Carnitine and coenzyme Q10 levels in individuals with Prader-Willi syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33887/fullpdf
Reference13 articles.
1. Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology;Bittel;Expert Rev Mol Med,2005
2. Coenzyme Q10 levels in Prader-Willi syndrome: Comparison with obese and non-obese subjects;Butler;Am J Med Genet Part A,2003
3. Regulation by carnitine of myocardial fatty acid and carbohydrate metabolism under normal and pathological conditions;Calvani;Basic Res Cardiol,2000
4. Prader-Willi syndrome;Cassidy;Eur J Hum Genet,2009
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1. Depletion and Supplementation of Coenzyme Q10 in Secondary Deficiency Disorders;Frontiers in Bioscience-Landmark;2022-12-19
2. Sleep Disorders in Children with Prader Willi Syndrome: Current Perspectives;Nature and Science of Sleep;2022-11
3. Benefits of multidisciplinary care in Prader-Willi syndrome;Expert Review of Endocrinology & Metabolism;2021-03-04
4. A multidisciplinary approach to the clinical management of Prader–Willi syndrome;Molecular Genetics & Genomic Medicine;2019-01-29
5. Excessive carbohydrate consumption and body mass index: the risk factors for type 2 diabetes mellitus in patients with Prader-Willi syndrome in Tamil Nadu population;The Journal of Basic and Applied Zoology;2018-12
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