Literature DB >> 10658173

Disorders of lipid metabolism in skeletal muscle.

V A Cwik1.   

Abstract

Lipid storage myopathies are typically present with recurrent episodes of myoglobinuria and hypoglycemia, triggered by fasting or infection. Dilated cardiomyopathy can occur. This article will discuss an approach to lipid storage myopathies and describes various forms of disorders by fatty acid oxidation.

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Year:  2000        PMID： 10658173     DOI： 10.1016/s0733-8619(05)70183-3

Source DB:  PubMed          Journal:  Neurol Clin        ISSN： 0733-8619            Impact factor:   3.806


  4 in total

Review 1.  Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.

Authors:  Harjot K Saini-Chohan; Ryan W Mitchell; Frédéric M Vaz; Teresa Zelinski; Grant M Hatch
Journal:  J Lipid Res       Date:  2011-11-07       Impact factor: 5.922

2.  Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency.

Authors:  R K J Olsen; M Pourfarzam; A A M Morris; R C Dias; I Knudsen; B S Andresen; N Gregersen; S E Olpin
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

3.  Muscle carnitine deficiency: adult onset lipid storage myopathy with sensory neuropathy.

Authors:  Wei Zhang; Jianting Miao; Guangyun Zhang; Rui Liu; Dawei Zhang; Qun Wan; Yingxin Yu; Gang Zhao; Zhuyi Li
Journal:  Neurol Sci       Date:  2009-09-19       Impact factor: 3.307

4.  Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency

Authors:  Jinru Zhang; Jingzhe Han; Yaye Wang; Yue Wu; Lixia Ma; Xueqin Song; Guang Ji
Journal:  Balkan Med J       Date:  2022-06-23       Impact factor: 3.570
  4 in total

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