Cystic fibrosis, pathophysiological and clinical aspects-Reference-Cited by-同舟云学术

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Cystic fibrosis, pathophysiological and clinical aspects

Published:1990-08 Issue:11 Volume:149 Page:742-751
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Neijens H. J.,Sinaasappel M.,de Groot R.,de Jongste J. C.,Overbeek S. E.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF01957271.pdf

Reference123 articles.

1. Abman SH, Ogle JW, Butler SN, Rumack CM, Accurso FJ (1988) Role of respiratory syncytial virus in early hospitalizations for respiratory distress of young infants with cystic fibrosis. J Pediatr 113:826–830

2. Ammitzoll T, Pederson SS, Espersen F, Schiller H (1988) Excretion of urinary collagen metabolites correlates to severity of pulmonary disease in cystic fibrosis. Acta Paediatr Scand 77:842–846

3. Andersen DH (1939) Cystic fibrosis of the pancreas and its relation to celciac disease: a clinical and pathological study. Am J Dis Child 56:344

4. Anonymous (1986) Supplementary nutrition in cystic fibrosis. Lancet I: 249–251

5. Bali B, Stableforth DE, Asquith P (1983) Prolonged small-intestinal transit time in cystic fibrosis. Br Med J 287:1011–1013

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2. Insulin-secretion abnormalities and clinical deterioration related to impaired glucose tolerance in cystic fibrosis;European Journal of Endocrinology;2005-02

3. High morbidity and mortality in cystic fibrosis patients compound heterozygous for 3905insT and ΔF508;European Respiratory Journal;2001-06-01

4. A Chest Wall Restrictor to Study Effects on Pulmonary Function and Exercise;Respiration;1999

5. Can the Histologic Changes of Cystic Fibrosis-Associated Hepatobiliary Disease be Predicted by Clinical Criteria?;Journal of Pediatric Gastroenterology & Nutrition;1997-07

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