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Vol. 5. Issue 2.
Pages 179-181 (March - April 1999)
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Vol. 5. Issue 2.
Pages 179-181 (March - April 1999)
Open Access
Fibrose Quística - Perspectivas do Pediatra*
Visits
4201
Celeste Barreto
Unidade de Pneumologia. Serviço de Pediatria. Hospital de Santa Maria
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BIBLIOGRAFIA
[1.]
S.C. Fitz Simmons.
The changing of Cystic Fibrosis.
J Pediatr, 122 (1993), pp. 1-9
[2.]
F.S. Colltns.
pp. 24-27
[3.]
L. Pereira, Bandeira, C. Barreto.
Aumento da esperança média de vida nos doentes com Fibrose Quistica·experiência do Centro de Fibrose Quistica da Unidade de Pneumologia do Hospital de Santa Maria.
Rev Port Pneumol, IV (1998), pp. 599-609
[4.]
R. Dinwiddie.
The diagnosis and nanagement of Paediauic respiratory Disease, pp. 177-222
[5.]
M. Farriel.
Nutricional Benefits of Neonatal screening for cystic Fibrosis.
The New Eng J Med, 14 (1997), pp. 963-969
[6.]
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Neonatal Screening Cystic Fibrosis Current Topics, pp. 303-317
[7.]
Manual De "Orientaçōes Para o Diagnostco e Acompanhamento Da Fibrose Quística".
elaborado pela OMS e International Cystic Fibrosis (Muciviscidosis) Association. traduzido e adaptado em Portugues, (1996),
[8.]
E. Kerem, B. Kerem.
Genotype-Phenotype Correlations in Cystic Fibrosis Pediatr.
Pulmonol., 22 (1996), pp. 387-395
[9.]
The Diagnosis of Cystic Fibrosis.
Consensus Statement. Cystic Fibrosis Foundation, (1996), pp. 1-15
[10.]
P. Loureiro, et al.
Geografia genética e prevenção da fibrose quistica em Portugal.
Arq. INSA, 20-21 (1994/1995), pp. 839-851
[11.]
S. Gallati.
Molecular genetics in paediatric diseases.
5, 2 (1997), pp. 214-235
[12.]
B.W. Ramsey.
Management of pulmonary disease in patients with Cystic Fibrosis.
N. Eng. J Med., 335 (1996), pp. 179-883
[13.]
B. Pamela, et al.
State of the Art Cystic Fibrosis.
Am J Respir Crit Care Med, 154 (1996), pp. 1229-1256
[14.]
J. Yankaskas, et al.
Cystic Fibrosis in Adults, pp. 465-476

Trabalho apresentado na Mesa Rcdonda "Fibrose Quistica"

Copyright © 1999. Sociedade Portuguesa de Pneumologia/SPP
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