Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings

Journal article

Peer reviewed

P Hudgson, W G Bradley and M Jenkison

Journal of the neurological sciences, Vol.16(3), pp.343-370

1972-07

PMID: 4114165

Abstract

Thyroid Function Tests

Humans

Middle Aged

Mitochondria, Muscle - metabolism

Male

Muscular Dystrophies - genetics

Muscles - pathology

Lipids - blood

Electrocardiography

Adult

Female

Electromyography

Muscles - metabolism

Child

Amino Acids - urine

Muscular Dystrophies - metabolism

Creatine Kinase - blood

Oxidative Phosphorylation

Lipid Metabolism

Lipoproteins - blood

Microscopy, Electron

Muscular Dystrophies - pathology

Pedigree

Adolescent

Aged

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Title: Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings
Creators: P Hudgson
W G Bradley
M Jenkison
Publication Details: Journal of the neurological sciences, Vol.16(3), pp.343-370
Publisher: Netherlands
Academic Unit: Miller School of Medicine; UMMG Department of Neurology; UMMG Dept of Neurology - Neuromuscular Disorders Div
Language: English
Resource Type: Journal article
PMID: 4114165
Record Identifier: 991031559908002976