McArdle's disease: Molecular genetics and metabolic consequences of the phenotype-Reference-Cited by-同舟云学术

McArdle's disease: Molecular genetics and metabolic consequences of the phenotype

Published:1995 Issue:S14 Volume:18 Page:S18-S22
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Beynon Robert J.,Bartram Clare,Hopkins Pam,Toescu Veronica,Gibson Henry,Phoenix Joanne,Edwards Richard H. T.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference24 articles.

1. McArdle's disease: a rare frameshift mutation in exon 1 of the muscle glycogen phosphorylase gene

2. McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases

4. : Protein degradation in normal and abnormal muscle?a study of glycogen phosphorylase, in (eds): Intracellular Protein Catabolism. Portland Press, London, pp 157-162.

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1. Carbohydrate Utilization and Disposal in Strength/Power Training and Sports: Examining the Underexamined;Nutritional Supplements in Sports and Exercise;2015

2. Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V);Cochrane Database of Systematic Reviews;2014-11-12

3. Forensic Aspects of Adult and General Neuropathology;Forensic Neuropathology, Third Edition;2014-05-07

4. Six-Digit CPK and Mildly Affected Renal Function in McArdle Disease;Case Reports in Pediatrics;2014

5. Carbohydrate and Muscle Glycogen Metabolism;Nutrition and Enhanced Sports Performance;2013