Journal Information
Vol. 33. Issue 1.
Pages 1-3 (January 1997)
Vol. 33. Issue 1.
Pages 1-3 (January 1997)
Full text access
Fibrosis quística en el adulto
Visits
4166
P. Morales Marín*
Servicio de Neumología. Hospital Universitario La Fe. Valencia
This item has received
Article information
Full text is only aviable in PDF
Bibliografía
[1.]
S.C. FitzSimmons.
The changing epidemiology of cystic fibrosis.
J Pediatr, 122 (1993), pp. 1-9
[2.]
P.A. Di Sant’Agnese, R.C. Taimo.
Pathogenesis and phisiopathology of CF of the pancreas.
N Engl J Med, 277 (1967), pp. 1.287-1.294
[3.]
P.A. Lewis.
The epidemiology of cystic fibrosis.
Cystic fibrosis, pp. 1-13
[4.]
F.S. Collins.
Cystic fibrosis: molecular biology and therapeutic implications.
Science, 256 (1992), pp. 774-779
[5.]
E.H. Oppenheimer, J.R. Esterly.
Pathology of cystic fibrosis: review of the literature and comparison with 146 autopsied cases.
Perspect Pediatr Pathol, 2 (1975), pp. 241-278
[6.]
A.G.F. Davidson.
Gastrointestinal and pancreatic disease in cystic fibrosis.
Cystic fibrosis, pp. 259-280
[7.]
M.W. Rostan, M. Berger.
Infection and inflammation of the lung in cystic fibrosis:.
Cystic fibrosis. Lung biology in health and disease, pp. 219-276
[8.]
B.W. Ramsey, P.M. Farrell, P. Pencharz.
Nutritional assessment and management in cystic fibrosis: a consensus report.
Am J Clin Nutr, 55 (1992), pp. 108-116
[9.]
B.W. Ramsey.
Drug therapy: mamagement of pulmonary disease in patients with cystic fibrosis.
N Engl J Med, 335 (1996), pp. 179-188
[10.]
Cystic Fibrosis Foundation Patient Registrary 1990.
Annual Data Report.
EE.UU, (1992),
[11.]
J.S. Elborn, D.J. Shale, J.R. Britton.
Cystic fibrosis: current survival and population estimates to the year 2000.
Thorax, 46 (1991), pp. 881-885
[12.]
M.E. Hodson.
Respiratory system. Adults.
Cystic fibrosis, pp. 237-258
[13.]
Cystic fibrosis in adults: recommendations for care in the UK Report of the Royal College of Phisicians of London. Londres, 1990.
[14.]
T.M. Egan.
Treatment of pneumothorax in the context of lung transplantation.
Pediatr Pulmonol, 8 (1992), pp. 82-84
[15.]
N.B. Sweezey, R.E. Fellows.
Bronchial artery embolisation for severe haemoptysis in cystic fibrosis.
Chest, 97 (1990), pp. 1.322-1.326
[16.]
E.J. Hiller.
Pathogenesis and management of aspergillosis in cystic fibrosis.
Arch Dis Child, 65 (1990), pp. 397-398
[17.]
Therapeutic approaches to cystic fibrosis.
Memorandum from a joint WHO/ICF(M). A meeting.
WHO Bulletin OMS, 72 (1994), pp. 341-352
[18.]
M. Szaff, N. Hoiby, E.W. Flensborg.
Frequent antibiotic therapy improves survival of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection.
Acta Paediatr Scand, 72 (1983), pp. 651-657
[19.]
A. Román, P. de Lucas, P. Morales, R. Lama, M.C. Carreño, A. Varela, Grupo de Trabajo de la SEPAR.
Normativa sobre el estudio y seguimiento del receptor de un trasplante pulmonar. Recomendaciones SEPAR.
Ediciones Doyma,, (1996), pp. 12-15
[20.]
B.P. Madden.
Lung transplantation.
Cystic fibrosis, pp. 329-346
[21.]
P. Morales, M.A. Martínez, P.J. Cordero, M.J. Cremades, J. Ferrer.
Fibrosis quística. Seguimiento en una unidad de adultos.
Arch Bron- coneumol, 32 (1996), pp. 94
Copyright © 1997. Sociedad Española de Neumología y Cirugía Torácica