Growth retardation and reduced growth hormone secretion in cystic fibrosis. Clinical observations from three CF centers-Reference-Cited by-同舟云学术

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Growth retardation and reduced growth hormone secretion in cystic fibrosis. Clinical observations from three CF centers

Published:2013-03 Issue:2 Volume:12 Page:165-169
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Ciro D'Orazio,Padoan Rita,Blau Hannah,Marostica Anna,Fuoti Maurizio,Volpi Sonia,Pilotta Alba,Meyerovitch Joseph,Sher Daniel,Assael Baroukh M.

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference32 articles.

1. Pigs and humans with cystic fibrosis have reduced IGF1 levels at birth;Rogan;PNAS,2010

2. Growth and long-term lung function in cystic fibrosis: a longitudinal study of patients diagnosed by neonatal screening;Assael;Pediatr Pulmonol,2009

3. Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis;Konstan;J Pediatr,2003

4. GH improves growth and clinical status in children with cystic fibrosis — a review of published studies;Hardin;Eur J Endocrinol,2004

5. Cystic fibrosis: terminology and diagnostic algorithms;De Boeck;Thorax,2006

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4. New insight into the importance of formulation variables on parenteral growth hormone preparations: potential effect on the injection-site pain;Frontiers in Endocrinology;2022-10-03

5. Physiological predictors of cardiorespiratory fitness in children and adolescents with cystic fibrosis without ventilatory limitation;Therapeutic Advances in Respiratory Disease;2022-01

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