Journal Information
Vol. 33. Issue 5.
Pages 247-250 (May 1997)
Share
Share
Download PDF
More article options
Vol. 33. Issue 5.
Pages 247-250 (May 1997)
Full text access
Importancia de la creación de unidades de fibrosis quística de adultos
Visits
4663
A. Salcedo*, M.A. Neira, A. Sequeiros, R. Girón
Unidad de Fibrosis Quística. Sección de Neumología. Hospital Infantil Niño Jesús. Madrid
This item has received
Article information
Full text is only aviable in PDF
Bibliografía
[1.]
W.J. Warwick.
The incidence of cystic fibrosis in Caucasian populations.
Helv Paediatr Acta, 33 (1978), pp. 117-125
[2.]
L.C. Tsui, M. Buchwald, D. Barker, J.C. Braman, R. Knowlton, J.W. Schumm, et al.
Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.
Science, 230 (1985), pp. 1.054-1.057
[3.]
J.M. Rommens, M.C. Iannuzzi, B.S. Kerem, M.L. Drumm, G. Melmer, M. Dean, et al.
Identification of the cystic fibrosis gene: chromosome walking and jumping.
Science, 245 (1989), pp. 1.059-1.065
[4.]
J.R. Riordan, J.M. Rommens, B.S. Kerem, N. Alón, R. Rozmahel, Z. Grzelczak, et al.
Identification of the cystic fibrosis gene: cloning and characterization of the complementary DNA.
Science, 245 (1989), pp. 1.066-1.073
[5.]
B.S. Kerem, J.M. Rommens, J.A. Buchanan, D. Markiewicz, T.K. Cox, A. Chakravarti, et al.
Identificación of the cystic fibrosis gene: genetic analysis.
Science, 245 (1989), pp. 1.073-1.080
[6.]
G. Romeo, M. Devoto.
Population analysis of the major mutation in cystic fibrosis.
Hum Genet, 85 (1990), pp. 391-445
[7.]
T. Casals, M. Chillón, J. Giménez, N. Morral, M.D. Ramos, A. Palacio, et al.
Fibrosis quística en población española: análisis genético y molecular de 500 familias.
An Esp Ped, 61 (1994), pp. 68-72
[8.]
M.P. Anderson, R.J. Gregory, S. Thompson, D.W. Souza, S. Paul, R.C. Mulligan, et al.
Demostration that CFTR is a chloride channel by alteration of its anion selectivity.
Science, 253 (1991), pp. 202-205
[9.]
W.J. Warwick, R.E. Pogue.
The prognosis for children with cystic fibrosis based on reasoned approaches to therapy: past, present and future.
J Asthma Res, 5 (1968), pp. 277-284
[10.]
Cystic Fibrosis Foundation.
Report of the 1978 Patient Registry.
The Foundation, (1980),
[11.]
W.J. Warwick, R.E. Pogue, H.U. Gerber, C.J. Nesbitt.
Survival pattems in cystic fibrosis.
J Chronic Dis, 28 (1975), pp. 609-622
[12.]
S.C. FitzSimmons.
The changing epidemiology of cystic fibrosis.
J Pediatr, 122 (1993), pp. 1-9
[13.]
J.S. Elbom, D.J. Shale, J.R. Britton.
Cystic fibrosis: current survival and population estimates to the year 2000.
Thorax, 46 (1991), pp. 881-885
[14.]
Patient Registry 1994 Annual Data Report.
Cystic Fibrosis Foundation, (1995),
[15.]
A.K. Webb.
Consumer, carer, provider, purchaser-developing care for adults with cystic fibrosis: a specialist Service.
Thorax, 49 (1994), pp. 291-292
[16.]
M. Robson, J. Abbott, K. Webb, M. Dodd, J. Walsworth-Bell.
A cost description of an adult cystic fibrosis unit and cost analyses of different categories of patients.
Thorax, 47 (1992), pp. 684-689
[17.]
Sterling N and CSAG Working group.
Cystic fibrosis. Access to and availability of specialist Services. Report of a Clinical Standards Advisory working group. Institute of Public and Environmental Health. University of Birmingham. Londres.
HMSO, (1993),
[18.]
M.E.H. Tumer-Warwick, Membership of the working party.
Cystic fibrosis in adults: recommendations for care of patients in the United Kingdom.
Royal College of Physicians, (1990),
[19.]
G.P. Marelich, C.E. Cross.
Cystic Fibrosis in adults. From researcher to practitioner.
West J Med, 164 (1996), pp. 321-324
[20.]
S. Walters, J. Britton, M.E. Hodson.
Hospital care for adults with cystic fibrosis: an overview and comparison between special cystic fibrosis clinics and general clinics using a patient questionnaire.
Thorax, 49 (1994), pp. 300-306
[21.]
A. Webb.
Communicating with young adults with cystic fibrosis.
Postgrad Med J, 71 (1995), pp. 385-389
[22.]
A. Salcedo.
Unidades de fibrosis quística. Organización y Funcionamiento.
An Esp Pediatr, 41 (1994), pp. 222-230
[23.]
S.Z. Nasr, C. Campbell, W. Howatt.
Transition program from pediatric to adult care for cystic fibrosis.
J Adolesc Health, 13 (1992), pp. 682-685
[24.]
R.W. Blum, D. Garell, C.H. Hodgman, T.W. Jorissen, N.A. Okinow, D.P. Orr, et al.
Transition from child-centered to adult health-care Systems for adolescents with chronic conditions. A position paper of the Society for Adolescent Medicine.
J Adolesc Health, 14 (1993), pp. 570-576
[25.]
D.S. Rosen.
Transition from pediatric to adult-oriented health care for the adolescent with chronic illness or disability.
Adolescent medicine: State of the art reviews, 5 (1994), pp. 241-248
[26.]
Conference Proceedings.
Moving on: transition from pediatric to adult health care.
J Adolesc Health, 1 (1995), pp. 1-32
[27.]
L.I. Landau.
Cystic fibrosis: transition from paediatric to adult physician's care.
Thorax, 50 (1995), pp. 1.031-1.032
[28.]
A. Salcedo, M.A. Neira, A. Sequeiros, R. Girón.
Transición etapa infantil a etapa adulta en fibrosis quística.
An Esp Ped, 45 (1996), pp. 455-458
Copyright © 1997. Sociedad Española de Neumología y Cirugía Torácica
Archivos de Bronconeumología
Article options
Tools

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