Ketoacidosis in Duchenne muscular dystrophy: A report on 4 cases
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference14 articles.
1. A systematic review and meta analyses on the epidemiology of Duchenne and Becker muscular dystrophy;Mah;Neuromuscul Disord,2014
2. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management;Bushby;Lancet Neurol.,2010
3. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987
4. Pathophysiology of Duchenne muscular dystrophy: current hypotheses;Deconinck;Pediatr Neurol,2007
5. Ketone body metabolism and its defects;Fukao;J Inherit Metab Dis,2014
Cited by 4 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. Life-threatening bowel complications in adults with Duchenne muscular dystrophy: a case series;Neuromuscular Disorders;2023-11
2. Endogenous De Novo Synthesis of Isopropanol Following Severe Non-Diabetic Ketoacidosis in a Patient With Duchenne Muscular Dystrophy;Journal of Endocrinology and Metabolism;2022-06
3. Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular Dystrophy;Journal of Neuromuscular Diseases;2021-11-02
4. Review article: Ketoacidosis in the emergency department;Emergency Medicine Australasia;2020-04-07
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