Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis-Reference-Cited by-同舟云学术

Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis

Published:2020-05-09 Issue:3 Volume:89 Page:653-659
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Zysman-Colman Zofia N.,Kilberg Marissa J.,Harrison Victor S.,Chesi Alessandra,Grant Struan F. A.,Mitchell Jonathan,Sheikh Saba,Hadjiliadis Denis,Rickels Michael R.,Rubenstein Ronald C.^ORCID,Kelly Andrea

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://www.nature.com/articles/s41390-020-0940-4.pdf

Reference35 articles.

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2. Borowitz, D., Baker, R. D. & Stallings, V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J. Pediatr. Gastroenterol. Nutr. 35, 246–259 (2002).

3. Blackman, S. M. & Tangpricha, V. Endocrine disorders in cystic fibrosis. Pediatr. Clin. North Am. 63, 699–708 (2016).

4. Landon, C. & Rosenfeld, R. G. Short stature and pubertal delay in male adolescents with cystic fibrosis. Androgen treatment. Am. J. Dis. Child 138, 388–391 (1984).

5. Davis, P. B. & Byard, P. J. Heterozygotes for cystic fibrosis: models for study of airway and autonomic reactivity. J. Appl. Physiol. 66, 2124–2128 (1989).

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