Resolution of severe hepatosteatosis in a cystic fibrosis patient with multifactorial choline deficiency: A case report-Reference-Cited by-同舟云学术

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Resolution of severe hepatosteatosis in a cystic fibrosis patient with multifactorial choline deficiency: A case report

Published:2021-09 Issue: Volume:89 Page:111348
ISSN:0899-9007
Container-title:Nutrition
language:en
Short-container-title:Nutrition

Author:

Bernhard Wolfgang^ORCID,Shunova Anna,Machann Jürgen,Grimmel Mona,Haack Tobias B.,Utz Philipp,Graepler-Mainka Ute

Publisher

Elsevier BV

Subject

Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism

Reference21 articles.

1. Cystic fibrosis—diagnosis and treatment;Naehrig;Dtsch Arztebl Int,2017

2. Gestational and neonatal characteristics of children with cystic fibrosis: a cohort study;Festini;J Pediatr,2005

3. Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening;Hoo;Thorax,2012

4. Respiratory rate in infants with cystic fibrosis throughout the first year of life and association with lung clearance index measured shortly after birth;Korten;J Cyst Fibros,2019

5. Liver disease in cystic fibrosis: a prospective study on incidence, risk factors, and outcome;Colombo;Hepatology,2002

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Different choline supplement metabolism in adults using deuterium labelling;European Journal of Nutrition;2023-02-25

2. Die Bedeutung von Cholin für die Entwicklung von Säuglingen und Kindern;Ernährung & Medizin;2022-12

3. Choline deficiency: Is it being recognized?;Nutrition;2022-02

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