array:24 [
  "pii" => "S1579212918300569"
  "issn" => "15792129"
  "doi" => "10.1016/j.arbr.2017.10.018"
  "estado" => "S300"
  "fechaPublicacion" => "2018-04-01"
  "aid" => "1749"
  "copyright" => "SEPAR"
  "copyrightAnyo" => "2017"
  "documento" => "simple-article"
  "crossmark" => 1
  "subdocumento" => "cor"
  "cita" => "Arch Bronconeumol. 2018;54:236"
  "abierto" => array:3 [
    "ES" => false
    "ES2" => false
    "LATM" => false
  ]
  "gratuito" => false
  "lecturas" => array:2 [
    "total" => 966
    "formatos" => array:3 [
      "EPUB" => 139
      "HTML" => 497
      "PDF" => 330
    ]
  ]
  "Traduccion" => array:1 [
    "en" => array:19 [
      "pii" => "S0300289617303952"
      "issn" => "03002896"
      "doi" => "10.1016/j.arbres.2017.10.006"
      "estado" => "S300"
      "fechaPublicacion" => "2018-04-01"
      "aid" => "1749"
      "copyright" => "SEPAR"
      "documento" => "simple-article"
      "crossmark" => 1
      "subdocumento" => "cor"
      "cita" => "Arch Bronconeumol. 2018;54:236"
      "abierto" => array:3 [
        "ES" => true
        "ES2" => true
        "LATM" => true
      ]
      "gratuito" => true
      "lecturas" => array:2 [
        "total" => 1452
        "formatos" => array:3 [
          "EPUB" => 157
          "HTML" => 717
          "PDF" => 578
        ]
      ]
      "en" => array:10 [
        "idiomaDefecto" => true
        "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
        "titulo" => "Molecular Detection of the Frequent Allele F52del in Alpha 1 Antitrypsin Deficiency"
        "tienePdf" => "en"
        "tieneTextoCompleto" => "en"
        "paginas" => array:1 [
          0 => array:1 [
            "paginaInicial" => "236"
          ]
        ]
        "titulosAlternativos" => array:1 [
          "es" => array:1 [
            "titulo" => "Detecci&#243;n molecular del alelo F52del frecuente en la deficiencia de alfa-1-antitripsina"
          ]
        ]
        "contieneTextoCompleto" => array:1 [
          "en" => true
        ]
        "contienePdf" => array:1 [
          "en" => true
        ]
        "autores" => array:1 [
          0 => array:2 [
            "autoresLista" => "Francisco Mart&#237;nez Bugallo, Juan Marco Figueira Gon&#231;alves, Mar&#237;a Dolores Mart&#237;n Mart&#237;nez"
            "autores" => array:3 [
              0 => array:2 [
                "nombre" => "Francisco"
                "apellidos" => "Mart&#237;nez Bugallo"
              ]
              1 => array:2 [
                "nombre" => "Juan Marco"
                "apellidos" => "Figueira Gon&#231;alves"
              ]
              2 => array:2 [
                "nombre" => "Mar&#237;a Dolores"
                "apellidos" => "Mart&#237;n Mart&#237;nez"
              ]
            ]
          ]
        ]
      ]
      "idiomaDefecto" => "en"
      "Traduccion" => array:1 [
        "en" => array:9 [
          "pii" => "S1579212918300569"
          "doi" => "10.1016/j.arbr.2017.10.018"
          "estado" => "S300"
          "subdocumento" => ""
          "abierto" => array:3 [
            "ES" => false
            "ES2" => false
            "LATM" => false
          ]
          "gratuito" => false
          "lecturas" => array:1 [
            "total" => 0
          ]
          "idiomaDefecto" => "en"
          "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300569?idApp=UINPBA00003Z"
        ]
      ]
      "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289617303952?idApp=UINPBA00003Z"
      "url" => "/03002896/0000005400000004/v2_201804150418/S0300289617303952/v2_201804150418/en/main.assets"
    ]
  ]
  "itemSiguiente" => array:19 [
    "pii" => "S1579212918300399"
    "issn" => "15792129"
    "doi" => "10.1016/j.arbr.2018.02.009"
    "estado" => "S300"
    "fechaPublicacion" => "2018-04-01"
    "aid" => "1754"
    "copyright" => "SEPAR"
    "documento" => "simple-article"
    "crossmark" => 1
    "subdocumento" => "cor"
    "cita" => "Arch Bronconeumol. 2018;54:237-8"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 1143
      "formatos" => array:3 [
        "EPUB" => 132
        "HTML" => 706
        "PDF" => 305
      ]
    ]
    "en" => array:10 [
      "idiomaDefecto" => true
      "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
      "titulo" => "The Role of FE<span class="elsevierStyleInf">NO</span> in the Diagnosis and Control of Asthma&#46; Expert Multidisciplinary Group Debate during the Asthma Meeting Point 2017"
      "tienePdf" => "en"
      "tieneTextoCompleto" => "en"
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "237"
          "paginaFinal" => "238"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "es" => array:1 [
          "titulo" => "Papel de la medici&#243;n de la FE<span class="elsevierStyleInf">NO</span> en el diagn&#243;stico y control del asma&#46; Debate del grupo multidisciplinar de expertos de la reuni&#243;n Asma Meeting Point 2017"
        ]
      ]
      "contieneTextoCompleto" => array:1 [
        "en" => true
      ]
      "contienePdf" => array:1 [
        "en" => true
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "Vicente Plaza, Borja G&#46; Cosio, Lu&#237;s Manuel Entrenas, Jos&#233; Mar&#237;a Olagu&#237;bel, Luis P&#233;rez de Llano, Santiago Quirce"
          "autores" => array:7 [
            0 => array:2 [
              "nombre" => "Vicente"
              "apellidos" => "Plaza"
            ]
            1 => array:2 [
              "nombre" => "Borja G&#46;"
              "apellidos" => "Cosio"
            ]
            2 => array:2 [
              "nombre" => "Lu&#237;s Manuel"
              "apellidos" => "Entrenas"
            ]
            3 => array:2 [
              "nombre" => "Jos&#233; Mar&#237;a"
              "apellidos" => "Olagu&#237;bel"
            ]
            4 => array:2 [
              "nombre" => "Luis"
              "apellidos" => "P&#233;rez de Llano"
            ]
            5 => array:2 [
              "nombre" => "Santiago"
              "apellidos" => "Quirce"
            ]
            6 => array:1 [
              "colaborador" => "members of the Multidisciplinary Group of Asthma Meeting Point &#40;AMP&#41; 2017"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "en"
    "Traduccion" => array:1 [
      "es" => array:9 [
        "pii" => "S0300289617304003"
        "doi" => "10.1016/j.arbres.2017.09.016"
        "estado" => "S300"
        "subdocumento" => ""
        "abierto" => array:3 [
          "ES" => true
          "ES2" => true
          "LATM" => true
        ]
        "gratuito" => true
        "lecturas" => array:1 [
          "total" => 0
        ]
        "idiomaDefecto" => "es"
        "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289617304003?idApp=UINPBA00003Z"
      ]
    ]
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300399?idApp=UINPBA00003Z"
    "url" => "/15792129/0000005400000004/v2_201804150412/S1579212918300399/v2_201804150412/en/main.assets"
  ]
  "itemAnterior" => array:19 [
    "pii" => "S1579212918300557"
    "issn" => "15792129"
    "doi" => "10.1016/j.arbr.2017.10.017"
    "estado" => "S300"
    "fechaPublicacion" => "2018-04-01"
    "aid" => "1747"
    "copyright" => "SEPAR"
    "documento" => "simple-article"
    "crossmark" => 1
    "subdocumento" => "cor"
    "cita" => "Arch Bronconeumol. 2018;54:235-6"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 932
      "formatos" => array:3 [
        "EPUB" => 106
        "HTML" => 549
        "PDF" => 277
      ]
    ]
    "en" => array:11 [
      "idiomaDefecto" => true
      "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
      "titulo" => "Successful Endoscopic Resection of an Endobronchial Lipoma Using a Percutaneous Gastrostomy Snare Device"
      "tienePdf" => "en"
      "tieneTextoCompleto" => "en"
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "235"
          "paginaFinal" => "236"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "es" => array:1 [
          "titulo" => "Resecci&#243;n endosc&#243;pica con &#233;xito de un lipoma endobronquial utilizando un dispositivo percut&#225;neo de asa para gastrostom&#237;a"
        ]
      ]
      "contieneTextoCompleto" => array:1 [
        "en" => true
      ]
      "contienePdf" => array:1 [
        "en" => true
      ]
      "resumenGrafico" => array:2 [
        "original" => 0
        "multimedia" => array:7 [
          "identificador" => "fig0005"
          "etiqueta" => "Figure 1"
          "tipo" => "MULTIMEDIAFIGURA"
          "mostrarFloat" => true
          "mostrarDisplay" => false
          "figura" => array:1 [
            0 => array:4 [
              "imagen" => "gr1.jpeg"
              "Alto" => 725
              "Ancho" => 2083
              "Tamanyo" => 152520
            ]
          ]
          "descripcion" => array:1 [
            "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; Computed tomography showing the endobronchial lipoma blocking the right main bronchus &#40;white arrow&#41;&#46; &#40;B&#41; Our snare mounted in the flexible bronchoscope&#46; &#40;C&#41; 15-mm lobulated soft tissue mass of almost excised lipoma&#46;</p>"
          ]
        ]
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "Ren&#233; Agust&#237;n Flores-Franco, Luis Fernando Gonz&#225;lez-Calzadillas, Stephanie Cota-Castro"
          "autores" => array:3 [
            0 => array:2 [
              "nombre" => "Ren&#233; Agust&#237;n"
              "apellidos" => "Flores-Franco"
            ]
            1 => array:2 [
              "nombre" => "Luis Fernando"
              "apellidos" => "Gonz&#225;lez-Calzadillas"
            ]
            2 => array:2 [
              "nombre" => "Stephanie"
              "apellidos" => "Cota-Castro"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "en"
    "Traduccion" => array:1 [
      "en" => array:9 [
        "pii" => "S0300289617303939"
        "doi" => "10.1016/j.arbres.2017.10.004"
        "estado" => "S300"
        "subdocumento" => ""
        "abierto" => array:3 [
          "ES" => true
          "ES2" => true
          "LATM" => true
        ]
        "gratuito" => true
        "lecturas" => array:1 [
          "total" => 0
        ]
        "idiomaDefecto" => "en"
        "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289617303939?idApp=UINPBA00003Z"
      ]
    ]
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300557?idApp=UINPBA00003Z"
    "url" => "/15792129/0000005400000004/v2_201804150412/S1579212918300557/v2_201804150412/en/main.assets"
  ]
  "en" => array:13 [
    "idiomaDefecto" => true
    "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
    "titulo" => "Molecular Detection of the Frequent Allele F52del in Alpha 1 Antitrypsin Deficiency"
    "tieneTextoCompleto" => true
    "saludo" => "Dear Editor&#44;"
    "paginas" => array:1 [
      0 => array:1 [
        "paginaInicial" => "236"
      ]
    ]
    "autores" => array:1 [
      0 => array:4 [
        "autoresLista" => "Francisco Mart&#237;nez Bugallo, Juan Marco Figueira Gon&#231;alves, Mar&#237;a Dolores Mart&#237;n Mart&#237;nez"
        "autores" => array:3 [
          0 => array:4 [
            "nombre" => "Francisco"
            "apellidos" => "Mart&#237;nez Bugallo"
            "email" => array:1 [
              0 => "fmarbug&#64;gobiernodecanarias&#46;org"
            ]
            "referencia" => array:2 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
              1 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">&#42;</span>"
                "identificador" => "cor0005"
              ]
            ]
          ]
          1 => array:3 [
            "nombre" => "Juan Marco"
            "apellidos" => "Figueira Gon&#231;alves"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">b</span>"
                "identificador" => "aff0010"
              ]
            ]
          ]
          2 => array:3 [
            "nombre" => "Mar&#237;a Dolores"
            "apellidos" => "Mart&#237;n Mart&#237;nez"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
        ]
        "afiliaciones" => array:2 [
          0 => array:3 [
            "entidad" => "Human Genetic Unit&#44; Clinical Analyses Services&#44; University Hospital Nuestra Se&#241;ora de Candelaria&#44; Santa Cruz de Tenerife&#44; Spain"
            "etiqueta" => "a"
            "identificador" => "aff0005"
          ]
          1 => array:3 [
            "entidad" => "Pneumology and Thoracic Surgery Service&#44; University Hospital Nuestra Se&#241;ora de Candelaria&#44; Santa Cruz de Tenerife&#44; Spain"
            "etiqueta" => "b"
            "identificador" => "aff0010"
          ]
        ]
        "correspondencia" => array:1 [
          0 => array:3 [
            "identificador" => "cor0005"
            "etiqueta" => "&#8270;"
            "correspondencia" => "Corresponding author&#46;"
          ]
        ]
      ]
    ]
    "titulosAlternativos" => array:1 [
      "es" => array:1 [
        "titulo" => "Detecci&#243;n molecular del alelo F52del frecuente en la deficiencia de alfa-1-antitripsina"
      ]
    ]
    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In some recent issues&#44; such as that of Belmonte et al&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> published in the International Journal of COPD&#44; have incorporated of the Mmalton allele-specific genotyping assay in the diagnostic algorithm of alpha-1 antitrypsin deficiency &#40;AATD&#41; to allow the clinical characterization of Mmalton individuals&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Current laboratory tests for AATD involve the determination of a combination of alpha-1 antitrypsin &#40;AAT&#41; serum levels&#44; AAT phenotyping by isoelectric focusing&#44; and an allele specific genotyping assay to detect the most prevalent&#44; S and Z&#44; deficiency alleles&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> However&#44; rare variants can only be detected by more complex techniques&#44; such as the use of allelic specific probes or sequencing of the SERPINA1 gene&#44; which are not available in all routine laboratories&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">A study published by Martinez Bugallo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> emphasizes that the Mmalton variant in the third most frequent variant deficiency in our island&#44; after S and Z alleles&#44; and with a higher prevalence than that described in the Iberian Peninsula&#46; Forty two patients with AAT values &#60;100<span class="elsevierStyleHsp" style=""></span>mg&#47;dL and with an inconclusive result in the genotype for PI&#42;S and PI&#42;Z underwent complete sequencing of the SERPINA1 gene&#46; Of the 42 patients studied&#44; at least one infrequent deficient allele was detected in 90&#46;4&#37; of the cases &#40;38 patients&#41;&#46; The most common deficient variant was Mmalton allele &#40;64&#46;2&#37;&#41;&#44; followed by Mpalermo allele &#40;16&#46;6&#37;&#41;&#44; both caused by the F52del mutation &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">The Mmalton and Mpalermo are two rare variants characterized by an F52del &#40;c&#46;226&#95;228delTTC&#41; mutation&#46; While the Mmalton allele must have derived from the normal M2 allele&#44; Mpalermo derives from the normal M1V&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">In our population&#44; Mpalermo represents 1 in 5 individuals with the F52del mutation&#44; and although the use of specific probes for the detection of this mutation seems to be a good diagnostic strategy&#44; it should be used as screening&#44; since that in our opinion it is necessary to perform the complete sequencing of SERPINA1 in all cases to make a more accurate diagnosis of these variants&#44; being necessary to confirm the presence of the base allele M2 or M1V in cis in these patients&#46;</p></span>"
    "pdfFichero" => "main.pdf"
    "tienePdf" => true
    "multimedia" => array:1 [
      0 => array:8 [
        "identificador" => "tbl0005"
        "etiqueta" => "Table 1"
        "tipo" => "MULTIMEDIATABLA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "detalles" => array:1 [
          0 => array:3 [
            "identificador" => "at1"
            "detalle" => "Table "
            "rol" => "short"
          ]
        ]
        "tabla" => array:1 [
          "tablatextoimagen" => array:1 [
            0 => array:2 [
              "tabla" => array:1 [
                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Genotype&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">N</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;M&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">17&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">40&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;S&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">16&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Z&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Mmalton&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">4&#46;8&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;M&#47;Mpalermo&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">14&#46;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;S&#47;Mpalermo&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;M&#47;Q0amersfoort&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Z&#47;Q0amersfoort&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Z&#47;Q0cardiff&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;MI&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">No deficitary allele&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">9&#46;5&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry  " colspan="3" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Overall&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">42&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">100&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
              ]
              "imagenFichero" => array:1 [
                0 => "xTab1720486.png"
              ]
            ]
          ]
        ]
        "descripcion" => array:1 [
          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Genotypes of Subjects with Rare Deficiency Alleles&#46;</p>"
        ]
      ]
    ]
    "bibliografia" => array:2 [
      "titulo" => "References"
      "seccion" => array:1 [
        0 => array:2 [
          "identificador" => "bibs0015"
          "bibliografiaReferencia" => array:5 [
            0 => array:3 [
              "identificador" => "bib0030"
              "etiqueta" => "1"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Application of a diagnostic algorithm for the rare deficient variant Mmalton of alpha-1-antitrypsin deficiency&#58; a new approach"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "I&#46; Belmonte"
                            1 => "M&#46; Barrecheguren"
                            2 => "R&#46;M&#46; L&#243;pez-Mart&#237;nez"
                            3 => "C&#46; Esquinas"
                            4 => "E&#46; Rodr&#237;guez"
                            5 => "M&#46; Miravitlles"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.2147/COPD.S115940"
                      "Revista" => array:6 [
                        "tituloSerie" => "Int J Chron Obstruct Pulmon Dis"
                        "fecha" => "2016"
                        "volumen" => "11"
                        "paginaInicial" => "2535"
                        "paginaFinal" => "2541"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/27877030"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            1 => array:3 [
              "identificador" => "bib0035"
              "etiqueta" => "2"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Diagnosis of alpha-1-antitrypsin deficiency&#58; an algorithm of quantification&#44; genotyping&#44; and phenotyping"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "M&#46;R&#46; Snyder"
                            1 => "J&#46;A&#46; Katzmann"
                            2 => "M&#46;L&#46; Butz"
                            3 => "P&#46; Yang"
                            4 => "D&#46;B&#46; Dawson"
                            5 => "K&#46;C&#46; Halling"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1373/clinchem.2006.072991"
                      "Revista" => array:6 [
                        "tituloSerie" => "Clin Chem"
                        "fecha" => "2006"
                        "volumen" => "52"
                        "paginaInicial" => "2236"
                        "paginaFinal" => "2242"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/17053153"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            2 => array:3 [
              "identificador" => "bib0040"
              "etiqueta" => "3"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Spectrum of alpha-1 antitrypsin deficiency mutations detected in Tenerife"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "F&#46; Mart&#237;nez Bugallo"
                            1 => "J&#46;M&#46; Figueira Gon&#231;alves"
                            2 => "M&#46;D&#46; Mart&#237;n Mart&#237;nez"
                            3 => "D&#46; D&#237;az P&#233;rez"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1016/j.arbres.2017.03.005"
                      "Revista" => array:6 [
                        "tituloSerie" => "Arch Bronconeumol"
                        "fecha" => "2017"
                        "volumen" => "53"
                        "paginaInicial" => "595"
                        "paginaFinal" => "596"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/28427797"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            3 => array:3 [
              "identificador" => "bib0045"
              "etiqueta" => "4"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Molecular basis of the liver and lung disease associated with the alpha 1-antitrypsin deficiency allele Mmalton"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "D&#46;T&#46; Curiel"
                            1 => "M&#46;D&#46; Holmes"
                            2 => "H&#46; Okayama"
                            3 => "M&#46;L&#46; Brantly"
                            4 => "C&#46; Vogelmeier"
                            5 => "W&#46;D&#46; Travis"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "J Biol Chem"
                        "fecha" => "1989"
                        "volumen" => "264"
                        "paginaInicial" => "13938"
                        "paginaFinal" => "13945"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/2788166"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            4 => array:3 [
              "identificador" => "bib0050"
              "etiqueta" => "5"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous&#44; compound heterozygous and heterozygous state"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "P&#46; Joly"
                            1 => "O&#46; Guillaud"
                            2 => "V&#46; Hervie"
                            3 => "A&#46; Francina"
                            4 => "J&#46;F&#46; Mornex"
                            5 => "C&#46; Chapuis-Cellier"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1186/s13023-015-0350-6"
                      "Revista" => array:5 [
                        "tituloSerie" => "Orphanet J Rare Dis"
                        "fecha" => "2015"
                        "volumen" => "10"
                        "paginaInicial" => "130"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/26446624"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
          ]
        ]
      ]
    ]
  ]
  "idiomaDefecto" => "en"
  "url" => "/15792129/0000005400000004/v2_201804150412/S1579212918300569/v2_201804150412/en/main.assets"
  "Apartado" => array:4 [
    "identificador" => "45358"
    "tipo" => "SECCION"
    "en" => array:2 [
      "titulo" => "Letters to the Editor"
      "idiomaDefecto" => true
    ]
    "idiomaDefecto" => "en"
  ]
  "PDF" => "https://static.elsevier.es/multimedia/15792129/0000005400000004/v2_201804150412/S1579212918300569/v2_201804150412/en/main.pdf?idApp=UINPBA00003Z&text.app=https://archbronconeumol.org/"
  "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300569?idApp=UINPBA00003Z"
]
Share
Journal Information

Statistics

Follow this link to access the full text of the article

Letter to the Editor
Molecular Detection of the Frequent Allele F52del in Alpha 1 Antitrypsin Deficiency
Detección molecular del alelo F52del frecuente en la deficiencia de alfa-1-antitripsina
Francisco Martínez Bugalloa,
Corresponding author
fmarbug@gobiernodecanarias.org

Corresponding author.
, Juan Marco Figueira Gonçalvesb, María Dolores Martín Martíneza
a Human Genetic Unit, Clinical Analyses Services, University Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain
b Pneumology and Thoracic Surgery Service, University Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain
Read
3373
Times
was read the article
1619
Total PDF
1754
Total HTML
Share statistics
 array:24 [
  "pii" => "S1579212918300569"
  "issn" => "15792129"
  "doi" => "10.1016/j.arbr.2017.10.018"
  "estado" => "S300"
  "fechaPublicacion" => "2018-04-01"
  "aid" => "1749"
  "copyright" => "SEPAR"
  "copyrightAnyo" => "2017"
  "documento" => "simple-article"
  "crossmark" => 1
  "subdocumento" => "cor"
  "cita" => "Arch Bronconeumol. 2018;54:236"
  "abierto" => array:3 [
    "ES" => false
    "ES2" => false
    "LATM" => false
  ]
  "gratuito" => false
  "lecturas" => array:2 [
    "total" => 966
    "formatos" => array:3 [
      "EPUB" => 139
      "HTML" => 497
      "PDF" => 330
    ]
  ]
  "Traduccion" => array:1 [
    "en" => array:19 [
      "pii" => "S0300289617303952"
      "issn" => "03002896"
      "doi" => "10.1016/j.arbres.2017.10.006"
      "estado" => "S300"
      "fechaPublicacion" => "2018-04-01"
      "aid" => "1749"
      "copyright" => "SEPAR"
      "documento" => "simple-article"
      "crossmark" => 1
      "subdocumento" => "cor"
      "cita" => "Arch Bronconeumol. 2018;54:236"
      "abierto" => array:3 [
        "ES" => true
        "ES2" => true
        "LATM" => true
      ]
      "gratuito" => true
      "lecturas" => array:2 [
        "total" => 1452
        "formatos" => array:3 [
          "EPUB" => 157
          "HTML" => 717
          "PDF" => 578
        ]
      ]
      "en" => array:10 [
        "idiomaDefecto" => true
        "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
        "titulo" => "Molecular Detection of the Frequent Allele F52del in Alpha 1 Antitrypsin Deficiency"
        "tienePdf" => "en"
        "tieneTextoCompleto" => "en"
        "paginas" => array:1 [
          0 => array:1 [
            "paginaInicial" => "236"
          ]
        ]
        "titulosAlternativos" => array:1 [
          "es" => array:1 [
            "titulo" => "Detecci&#243;n molecular del alelo F52del frecuente en la deficiencia de alfa-1-antitripsina"
          ]
        ]
        "contieneTextoCompleto" => array:1 [
          "en" => true
        ]
        "contienePdf" => array:1 [
          "en" => true
        ]
        "autores" => array:1 [
          0 => array:2 [
            "autoresLista" => "Francisco Mart&#237;nez Bugallo, Juan Marco Figueira Gon&#231;alves, Mar&#237;a Dolores Mart&#237;n Mart&#237;nez"
            "autores" => array:3 [
              0 => array:2 [
                "nombre" => "Francisco"
                "apellidos" => "Mart&#237;nez Bugallo"
              ]
              1 => array:2 [
                "nombre" => "Juan Marco"
                "apellidos" => "Figueira Gon&#231;alves"
              ]
              2 => array:2 [
                "nombre" => "Mar&#237;a Dolores"
                "apellidos" => "Mart&#237;n Mart&#237;nez"
              ]
            ]
          ]
        ]
      ]
      "idiomaDefecto" => "en"
      "Traduccion" => array:1 [
        "en" => array:9 [
          "pii" => "S1579212918300569"
          "doi" => "10.1016/j.arbr.2017.10.018"
          "estado" => "S300"
          "subdocumento" => ""
          "abierto" => array:3 [
            "ES" => false
            "ES2" => false
            "LATM" => false
          ]
          "gratuito" => false
          "lecturas" => array:1 [
            "total" => 0
          ]
          "idiomaDefecto" => "en"
          "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300569?idApp=UINPBA00003Z"
        ]
      ]
      "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289617303952?idApp=UINPBA00003Z"
      "url" => "/03002896/0000005400000004/v2_201804150418/S0300289617303952/v2_201804150418/en/main.assets"
    ]
  ]
  "itemSiguiente" => array:19 [
    "pii" => "S1579212918300399"
    "issn" => "15792129"
    "doi" => "10.1016/j.arbr.2018.02.009"
    "estado" => "S300"
    "fechaPublicacion" => "2018-04-01"
    "aid" => "1754"
    "copyright" => "SEPAR"
    "documento" => "simple-article"
    "crossmark" => 1
    "subdocumento" => "cor"
    "cita" => "Arch Bronconeumol. 2018;54:237-8"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 1143
      "formatos" => array:3 [
        "EPUB" => 132
        "HTML" => 706
        "PDF" => 305
      ]
    ]
    "en" => array:10 [
      "idiomaDefecto" => true
      "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
      "titulo" => "The Role of FE<span class="elsevierStyleInf">NO</span> in the Diagnosis and Control of Asthma&#46; Expert Multidisciplinary Group Debate during the Asthma Meeting Point 2017"
      "tienePdf" => "en"
      "tieneTextoCompleto" => "en"
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "237"
          "paginaFinal" => "238"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "es" => array:1 [
          "titulo" => "Papel de la medici&#243;n de la FE<span class="elsevierStyleInf">NO</span> en el diagn&#243;stico y control del asma&#46; Debate del grupo multidisciplinar de expertos de la reuni&#243;n Asma Meeting Point 2017"
        ]
      ]
      "contieneTextoCompleto" => array:1 [
        "en" => true
      ]
      "contienePdf" => array:1 [
        "en" => true
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "Vicente Plaza, Borja G&#46; Cosio, Lu&#237;s Manuel Entrenas, Jos&#233; Mar&#237;a Olagu&#237;bel, Luis P&#233;rez de Llano, Santiago Quirce"
          "autores" => array:7 [
            0 => array:2 [
              "nombre" => "Vicente"
              "apellidos" => "Plaza"
            ]
            1 => array:2 [
              "nombre" => "Borja G&#46;"
              "apellidos" => "Cosio"
            ]
            2 => array:2 [
              "nombre" => "Lu&#237;s Manuel"
              "apellidos" => "Entrenas"
            ]
            3 => array:2 [
              "nombre" => "Jos&#233; Mar&#237;a"
              "apellidos" => "Olagu&#237;bel"
            ]
            4 => array:2 [
              "nombre" => "Luis"
              "apellidos" => "P&#233;rez de Llano"
            ]
            5 => array:2 [
              "nombre" => "Santiago"
              "apellidos" => "Quirce"
            ]
            6 => array:1 [
              "colaborador" => "members of the Multidisciplinary Group of Asthma Meeting Point &#40;AMP&#41; 2017"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "en"
    "Traduccion" => array:1 [
      "es" => array:9 [
        "pii" => "S0300289617304003"
        "doi" => "10.1016/j.arbres.2017.09.016"
        "estado" => "S300"
        "subdocumento" => ""
        "abierto" => array:3 [
          "ES" => true
          "ES2" => true
          "LATM" => true
        ]
        "gratuito" => true
        "lecturas" => array:1 [
          "total" => 0
        ]
        "idiomaDefecto" => "es"
        "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289617304003?idApp=UINPBA00003Z"
      ]
    ]
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300399?idApp=UINPBA00003Z"
    "url" => "/15792129/0000005400000004/v2_201804150412/S1579212918300399/v2_201804150412/en/main.assets"
  ]
  "itemAnterior" => array:19 [
    "pii" => "S1579212918300557"
    "issn" => "15792129"
    "doi" => "10.1016/j.arbr.2017.10.017"
    "estado" => "S300"
    "fechaPublicacion" => "2018-04-01"
    "aid" => "1747"
    "copyright" => "SEPAR"
    "documento" => "simple-article"
    "crossmark" => 1
    "subdocumento" => "cor"
    "cita" => "Arch Bronconeumol. 2018;54:235-6"
    "abierto" => array:3 [
      "ES" => false
      "ES2" => false
      "LATM" => false
    ]
    "gratuito" => false
    "lecturas" => array:2 [
      "total" => 932
      "formatos" => array:3 [
        "EPUB" => 106
        "HTML" => 549
        "PDF" => 277
      ]
    ]
    "en" => array:11 [
      "idiomaDefecto" => true
      "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
      "titulo" => "Successful Endoscopic Resection of an Endobronchial Lipoma Using a Percutaneous Gastrostomy Snare Device"
      "tienePdf" => "en"
      "tieneTextoCompleto" => "en"
      "paginas" => array:1 [
        0 => array:2 [
          "paginaInicial" => "235"
          "paginaFinal" => "236"
        ]
      ]
      "titulosAlternativos" => array:1 [
        "es" => array:1 [
          "titulo" => "Resecci&#243;n endosc&#243;pica con &#233;xito de un lipoma endobronquial utilizando un dispositivo percut&#225;neo de asa para gastrostom&#237;a"
        ]
      ]
      "contieneTextoCompleto" => array:1 [
        "en" => true
      ]
      "contienePdf" => array:1 [
        "en" => true
      ]
      "resumenGrafico" => array:2 [
        "original" => 0
        "multimedia" => array:7 [
          "identificador" => "fig0005"
          "etiqueta" => "Figure 1"
          "tipo" => "MULTIMEDIAFIGURA"
          "mostrarFloat" => true
          "mostrarDisplay" => false
          "figura" => array:1 [
            0 => array:4 [
              "imagen" => "gr1.jpeg"
              "Alto" => 725
              "Ancho" => 2083
              "Tamanyo" => 152520
            ]
          ]
          "descripcion" => array:1 [
            "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; Computed tomography showing the endobronchial lipoma blocking the right main bronchus &#40;white arrow&#41;&#46; &#40;B&#41; Our snare mounted in the flexible bronchoscope&#46; &#40;C&#41; 15-mm lobulated soft tissue mass of almost excised lipoma&#46;</p>"
          ]
        ]
      ]
      "autores" => array:1 [
        0 => array:2 [
          "autoresLista" => "Ren&#233; Agust&#237;n Flores-Franco, Luis Fernando Gonz&#225;lez-Calzadillas, Stephanie Cota-Castro"
          "autores" => array:3 [
            0 => array:2 [
              "nombre" => "Ren&#233; Agust&#237;n"
              "apellidos" => "Flores-Franco"
            ]
            1 => array:2 [
              "nombre" => "Luis Fernando"
              "apellidos" => "Gonz&#225;lez-Calzadillas"
            ]
            2 => array:2 [
              "nombre" => "Stephanie"
              "apellidos" => "Cota-Castro"
            ]
          ]
        ]
      ]
    ]
    "idiomaDefecto" => "en"
    "Traduccion" => array:1 [
      "en" => array:9 [
        "pii" => "S0300289617303939"
        "doi" => "10.1016/j.arbres.2017.10.004"
        "estado" => "S300"
        "subdocumento" => ""
        "abierto" => array:3 [
          "ES" => true
          "ES2" => true
          "LATM" => true
        ]
        "gratuito" => true
        "lecturas" => array:1 [
          "total" => 0
        ]
        "idiomaDefecto" => "en"
        "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0300289617303939?idApp=UINPBA00003Z"
      ]
    ]
    "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300557?idApp=UINPBA00003Z"
    "url" => "/15792129/0000005400000004/v2_201804150412/S1579212918300557/v2_201804150412/en/main.assets"
  ]
  "en" => array:13 [
    "idiomaDefecto" => true
    "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>"
    "titulo" => "Molecular Detection of the Frequent Allele F52del in Alpha 1 Antitrypsin Deficiency"
    "tieneTextoCompleto" => true
    "saludo" => "Dear Editor&#44;"
    "paginas" => array:1 [
      0 => array:1 [
        "paginaInicial" => "236"
      ]
    ]
    "autores" => array:1 [
      0 => array:4 [
        "autoresLista" => "Francisco Mart&#237;nez Bugallo, Juan Marco Figueira Gon&#231;alves, Mar&#237;a Dolores Mart&#237;n Mart&#237;nez"
        "autores" => array:3 [
          0 => array:4 [
            "nombre" => "Francisco"
            "apellidos" => "Mart&#237;nez Bugallo"
            "email" => array:1 [
              0 => "fmarbug&#64;gobiernodecanarias&#46;org"
            ]
            "referencia" => array:2 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
              1 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">&#42;</span>"
                "identificador" => "cor0005"
              ]
            ]
          ]
          1 => array:3 [
            "nombre" => "Juan Marco"
            "apellidos" => "Figueira Gon&#231;alves"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">b</span>"
                "identificador" => "aff0010"
              ]
            ]
          ]
          2 => array:3 [
            "nombre" => "Mar&#237;a Dolores"
            "apellidos" => "Mart&#237;n Mart&#237;nez"
            "referencia" => array:1 [
              0 => array:2 [
                "etiqueta" => "<span class="elsevierStyleSup">a</span>"
                "identificador" => "aff0005"
              ]
            ]
          ]
        ]
        "afiliaciones" => array:2 [
          0 => array:3 [
            "entidad" => "Human Genetic Unit&#44; Clinical Analyses Services&#44; University Hospital Nuestra Se&#241;ora de Candelaria&#44; Santa Cruz de Tenerife&#44; Spain"
            "etiqueta" => "a"
            "identificador" => "aff0005"
          ]
          1 => array:3 [
            "entidad" => "Pneumology and Thoracic Surgery Service&#44; University Hospital Nuestra Se&#241;ora de Candelaria&#44; Santa Cruz de Tenerife&#44; Spain"
            "etiqueta" => "b"
            "identificador" => "aff0010"
          ]
        ]
        "correspondencia" => array:1 [
          0 => array:3 [
            "identificador" => "cor0005"
            "etiqueta" => "&#8270;"
            "correspondencia" => "Corresponding author&#46;"
          ]
        ]
      ]
    ]
    "titulosAlternativos" => array:1 [
      "es" => array:1 [
        "titulo" => "Detecci&#243;n molecular del alelo F52del frecuente en la deficiencia de alfa-1-antitripsina"
      ]
    ]
    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In some recent issues&#44; such as that of Belmonte et al&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> published in the International Journal of COPD&#44; have incorporated of the Mmalton allele-specific genotyping assay in the diagnostic algorithm of alpha-1 antitrypsin deficiency &#40;AATD&#41; to allow the clinical characterization of Mmalton individuals&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Current laboratory tests for AATD involve the determination of a combination of alpha-1 antitrypsin &#40;AAT&#41; serum levels&#44; AAT phenotyping by isoelectric focusing&#44; and an allele specific genotyping assay to detect the most prevalent&#44; S and Z&#44; deficiency alleles&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> However&#44; rare variants can only be detected by more complex techniques&#44; such as the use of allelic specific probes or sequencing of the SERPINA1 gene&#44; which are not available in all routine laboratories&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">A study published by Martinez Bugallo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> emphasizes that the Mmalton variant in the third most frequent variant deficiency in our island&#44; after S and Z alleles&#44; and with a higher prevalence than that described in the Iberian Peninsula&#46; Forty two patients with AAT values &#60;100<span class="elsevierStyleHsp" style=""></span>mg&#47;dL and with an inconclusive result in the genotype for PI&#42;S and PI&#42;Z underwent complete sequencing of the SERPINA1 gene&#46; Of the 42 patients studied&#44; at least one infrequent deficient allele was detected in 90&#46;4&#37; of the cases &#40;38 patients&#41;&#46; The most common deficient variant was Mmalton allele &#40;64&#46;2&#37;&#41;&#44; followed by Mpalermo allele &#40;16&#46;6&#37;&#41;&#44; both caused by the F52del mutation &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">The Mmalton and Mpalermo are two rare variants characterized by an F52del &#40;c&#46;226&#95;228delTTC&#41; mutation&#46; While the Mmalton allele must have derived from the normal M2 allele&#44; Mpalermo derives from the normal M1V&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">In our population&#44; Mpalermo represents 1 in 5 individuals with the F52del mutation&#44; and although the use of specific probes for the detection of this mutation seems to be a good diagnostic strategy&#44; it should be used as screening&#44; since that in our opinion it is necessary to perform the complete sequencing of SERPINA1 in all cases to make a more accurate diagnosis of these variants&#44; being necessary to confirm the presence of the base allele M2 or M1V in cis in these patients&#46;</p></span>"
    "pdfFichero" => "main.pdf"
    "tienePdf" => true
    "multimedia" => array:1 [
      0 => array:8 [
        "identificador" => "tbl0005"
        "etiqueta" => "Table 1"
        "tipo" => "MULTIMEDIATABLA"
        "mostrarFloat" => true
        "mostrarDisplay" => false
        "detalles" => array:1 [
          0 => array:3 [
            "identificador" => "at1"
            "detalle" => "Table "
            "rol" => "short"
          ]
        ]
        "tabla" => array:1 [
          "tablatextoimagen" => array:1 [
            0 => array:2 [
              "tabla" => array:1 [
                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Genotype&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">N</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">&#37;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;M&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">17&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">40&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;S&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">16&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Z&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Mmalton&#47;Mmalton&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">4&#46;8&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;M&#47;Mpalermo&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">14&#46;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;S&#47;Mpalermo&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;M&#47;Q0amersfoort&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Z&#47;Q0amersfoort&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;Z&#47;Q0cardiff&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">PI&#42;MI&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">2&#46;4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">No deficitary allele&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">4&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">9&#46;5&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry  " colspan="3" align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Overall&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">42&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="char" valign="top">100&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
              ]
              "imagenFichero" => array:1 [
                0 => "xTab1720486.png"
              ]
            ]
          ]
        ]
        "descripcion" => array:1 [
          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Genotypes of Subjects with Rare Deficiency Alleles&#46;</p>"
        ]
      ]
    ]
    "bibliografia" => array:2 [
      "titulo" => "References"
      "seccion" => array:1 [
        0 => array:2 [
          "identificador" => "bibs0015"
          "bibliografiaReferencia" => array:5 [
            0 => array:3 [
              "identificador" => "bib0030"
              "etiqueta" => "1"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Application of a diagnostic algorithm for the rare deficient variant Mmalton of alpha-1-antitrypsin deficiency&#58; a new approach"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "I&#46; Belmonte"
                            1 => "M&#46; Barrecheguren"
                            2 => "R&#46;M&#46; L&#243;pez-Mart&#237;nez"
                            3 => "C&#46; Esquinas"
                            4 => "E&#46; Rodr&#237;guez"
                            5 => "M&#46; Miravitlles"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.2147/COPD.S115940"
                      "Revista" => array:6 [
                        "tituloSerie" => "Int J Chron Obstruct Pulmon Dis"
                        "fecha" => "2016"
                        "volumen" => "11"
                        "paginaInicial" => "2535"
                        "paginaFinal" => "2541"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/27877030"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            1 => array:3 [
              "identificador" => "bib0035"
              "etiqueta" => "2"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Diagnosis of alpha-1-antitrypsin deficiency&#58; an algorithm of quantification&#44; genotyping&#44; and phenotyping"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "M&#46;R&#46; Snyder"
                            1 => "J&#46;A&#46; Katzmann"
                            2 => "M&#46;L&#46; Butz"
                            3 => "P&#46; Yang"
                            4 => "D&#46;B&#46; Dawson"
                            5 => "K&#46;C&#46; Halling"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1373/clinchem.2006.072991"
                      "Revista" => array:6 [
                        "tituloSerie" => "Clin Chem"
                        "fecha" => "2006"
                        "volumen" => "52"
                        "paginaInicial" => "2236"
                        "paginaFinal" => "2242"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/17053153"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            2 => array:3 [
              "identificador" => "bib0040"
              "etiqueta" => "3"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Spectrum of alpha-1 antitrypsin deficiency mutations detected in Tenerife"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "F&#46; Mart&#237;nez Bugallo"
                            1 => "J&#46;M&#46; Figueira Gon&#231;alves"
                            2 => "M&#46;D&#46; Mart&#237;n Mart&#237;nez"
                            3 => "D&#46; D&#237;az P&#233;rez"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1016/j.arbres.2017.03.005"
                      "Revista" => array:6 [
                        "tituloSerie" => "Arch Bronconeumol"
                        "fecha" => "2017"
                        "volumen" => "53"
                        "paginaInicial" => "595"
                        "paginaFinal" => "596"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/28427797"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            3 => array:3 [
              "identificador" => "bib0045"
              "etiqueta" => "4"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Molecular basis of the liver and lung disease associated with the alpha 1-antitrypsin deficiency allele Mmalton"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => true
                          "autores" => array:6 [
                            0 => "D&#46;T&#46; Curiel"
                            1 => "M&#46;D&#46; Holmes"
                            2 => "H&#46; Okayama"
                            3 => "M&#46;L&#46; Brantly"
                            4 => "C&#46; Vogelmeier"
                            5 => "W&#46;D&#46; Travis"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:1 [
                      "Revista" => array:6 [
                        "tituloSerie" => "J Biol Chem"
                        "fecha" => "1989"
                        "volumen" => "264"
                        "paginaInicial" => "13938"
                        "paginaFinal" => "13945"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/2788166"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
            4 => array:3 [
              "identificador" => "bib0050"
              "etiqueta" => "5"
              "referencia" => array:1 [
                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous&#44; compound heterozygous and heterozygous state"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:6 [
                            0 => "P&#46; Joly"
                            1 => "O&#46; Guillaud"
                            2 => "V&#46; Hervie"
                            3 => "A&#46; Francina"
                            4 => "J&#46;F&#46; Mornex"
                            5 => "C&#46; Chapuis-Cellier"
                          ]
                        ]
                      ]
                    ]
                  ]
                  "host" => array:1 [
                    0 => array:2 [
                      "doi" => "10.1186/s13023-015-0350-6"
                      "Revista" => array:5 [
                        "tituloSerie" => "Orphanet J Rare Dis"
                        "fecha" => "2015"
                        "volumen" => "10"
                        "paginaInicial" => "130"
                        "link" => array:1 [
                          0 => array:2 [
                            "url" => "https://www.ncbi.nlm.nih.gov/pubmed/26446624"
                            "web" => "Medline"
                          ]
                        ]
                      ]
                    ]
                  ]
                ]
              ]
            ]
          ]
        ]
      ]
    ]
  ]
  "idiomaDefecto" => "en"
  "url" => "/15792129/0000005400000004/v2_201804150412/S1579212918300569/v2_201804150412/en/main.assets"
  "Apartado" => array:4 [
    "identificador" => "45358"
    "tipo" => "SECCION"
    "en" => array:2 [
      "titulo" => "Letters to the Editor"
      "idiomaDefecto" => true
    ]
    "idiomaDefecto" => "en"
  ]
  "PDF" => "https://static.elsevier.es/multimedia/15792129/0000005400000004/v2_201804150412/S1579212918300569/v2_201804150412/en/main.pdf?idApp=UINPBA00003Z&text.app=https://archbronconeumol.org/"
  "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1579212918300569?idApp=UINPBA00003Z"
]
Article information
ISSN: 15792129
Original language: English
The statistics are updated each day
Year/Month Html Pdf Total
2024 November 5 3 8
2024 October 29 19 48
2024 September 26 21 47
2024 August 44 49 93
2024 July 26 27 53
2024 June 32 18 50
2024 May 42 29 71
2024 April 23 27 50
2024 March 29 19 48
2024 February 29 28 57
2023 December 1 2 3
2023 March 6 6 12
2023 February 24 25 49
2023 January 20 27 47
2022 December 25 26 51
2022 November 33 22 55
2022 October 37 29 66
2022 September 30 26 56
2022 August 33 43 76
2022 July 24 42 66
2022 June 24 35 59
2022 May 31 38 69
2022 April 15 33 48
2022 March 22 29 51
2022 February 30 26 56
2022 January 28 26 54
2021 December 28 37 65
2021 November 39 37 76
2021 October 38 51 89
2021 September 22 37 59
2021 August 21 37 58
2021 July 22 24 46
2021 June 24 30 54
2021 May 31 46 77
2021 April 78 106 184
2021 March 40 21 61
2021 February 23 28 51
2021 January 23 14 37
2020 December 21 17 38
2020 November 27 19 46
2020 October 18 20 38
2020 September 19 10 29
2020 August 19 12 31
2020 July 19 16 35
2020 June 14 9 23
2020 May 14 10 24
2020 April 25 15 40
2020 March 11 6 17
2020 February 32 23 55
2020 January 19 21 40
2019 December 39 12 51
2019 November 30 22 52
2019 October 14 14 28
2019 September 16 17 33
2019 August 20 21 41
2019 July 27 25 52
2019 June 20 16 36
2019 May 27 25 52
2019 April 20 18 38
2019 March 33 18 51
2019 February 32 21 53
2019 January 36 14 50
2018 December 39 19 58
2018 November 45 32 77
2018 October 59 22 81
2018 September 2 2 4
Show all

Follow this link to access the full text of the article

Archivos de Bronconeumología

Are you a health professional able to prescribe or dispense drugs?