Mitochondrial myopathy and familial thiamine deficiency

Muscle and Nerve

Volumn 23, Issue 7, 2000, Pages 1069-1075

  Sato, Yoshihiro ^a,d   Nakagawa, Masanori ^b   Higuchi, Itsuro ^b   Osame, Mitsuhiro ^b   Naito, Etsuo ^c   Oizumi, Kotaro ^a  

^a KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b KAGOSHIMA UNIVERSITY   (Japan)

^c UNIVERSITY OF TOKUSHIMA   (Japan)

^d KURUME UNIVERSITY MEDICAL CENTER   (Japan)

Author keywords

MELAS; Mitochondrial DNA; Pyruvate; Skeletal myopathy; Thiamine

Indexed keywords

BENFOTIAMINE; CREATINE KINASE MB; LACTIC ACID; MITOCHONDRIAL DNA; PYRUVIC ACID; THIAMINE;

ADULT; ARTICLE; CASE REPORT; ELECTRON TRANSPORT; ENZYME ACTIVITY; FAMILIAL DISEASE; GENE MUTATION; HUMAN; HUMAN TISSUE; MALE; MITOCHONDRIAL MYOPATHY; PRIORITY JOURNAL; SLOW MUSCLE FIBER; THIAMINE DEFICIENCY; VITAMIN METABOLISM; VITAMIN SUPPLEMENTATION;

ADULT; ATROPHY; DNA, MITOCHONDRIAL; ELECTROCARDIOGRAPHY; FEMALE; HEMODYNAMIC PROCESSES; HUMANS; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL MYOPATHIES; MUSCLE WEAKNESS; MUSCLE, SKELETAL; THIAMINE; THIAMINE DEFICIENCY;

EID: 0033935842     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-4598(200007)23:7<1069::AID-MUS9>3.0.CO;2-0     Document Type: Article

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