Impaired glucose tolerance, body mass index and respiratory function in patients with cystic fibrosis: A systematic review
Author:
Affiliation:
1. Division of Pediatric Pulmonology Michigan Medicine Ann Arbor Michigan
2. Faculty, Nutrition & Dietetics, Department of Human Environmental Studies Central Michigan University The Villages Florida
Publisher
Wiley
Subject
Genetics(clinical),Pulmonary and Respiratory Medicine,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/crj.13019
Reference30 articles.
1. Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders
2. Clinical Care Guidelines for Cystic Fibrosis-Related Diabetes: A position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society
3. Nutritional management of cystic fibrosis ‐ an update for the 21st century;Collins S;Paediatr Respir Rev,2018
4. CF-related diabetes: Containing the metabolic miscreant of cystic fibrosis
5. Cystic-fibrosis related-diabetes (CFRD) is preceded by and associated with growth failure and deteriorating lung function
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2. Significance of fructosamine in the diagnosis of carbohydrate metabolism disorders in children with cystic fibrosis;Meditsinskiy sovet = Medical Council;2022-03-03
3. Clinical implications of fungal isolation from sputum in adult patients with cystic fibrosis;TURKISH JOURNAL OF MEDICAL SCIENCES;2021-06-28
4. Detection and Management of Early Glucose Abnormalities in Cystic Fibrosis;Cystic Fibrosis - Facts, Management and Advances;2021-06-09
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