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Volumn 56, Issue 3, 2008, Pages 391-393
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Lipid storage myopathies with unusual clinical manifestations
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Author keywords
Carnitine therapy; Lipid storage myopathy; Muscle biopsy
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Indexed keywords
AMYLASE;
ASPARTIC ACID;
CARNITINE;
CREATINE KINASE;
CYTOCHROME B;
GLUCOSE;
IMMUNOGLOBULIN;
TRANSFER RNA;
TRIACYLGLYCEROL LIPASE;
UBIQUINONE;
ABDOMINAL PAIN;
ACUTE PANCREATITIS;
ADULT;
AMYLASE BLOOD LEVEL;
ARTICLE;
ARTIFICIAL VENTILATION;
CARNITINE DEFICIENCY;
CASE REPORT;
CREATINE KINASE BLOOD LEVEL;
DRUG WITHDRAWAL;
ELECTROMYOGRAM;
FEMALE;
FOLLOW UP;
GENE MUTATION;
GENE SEQUENCE;
GENETIC ANALYSIS;
GENETIC SCREENING;
GLUCOSE BLOOD LEVEL;
GUILLAIN BARRE SYNDROME;
HOSPITAL DISCHARGE;
HOSPITAL READMISSION;
HUMAN;
HUMAN TISSUE;
LIMB WEAKNESS;
LIVER FUNCTION TEST;
MITOCHONDRIAL GENE;
MITOCHONDRIAL MYOPATHY;
MUSCLE ATROPHY;
MUSCLE BIOPSY;
MUSCLE WEAKNESS;
MUSCULAR DYSTROPHY;
PHYSICAL EXAMINATION;
POLYMERASE CHAIN REACTION;
TENDON REFLEX;
TREATMENT RESPONSE;
TRIACYLGLYCEROL LIPASE BLOOD LEVEL;
VOMITING;
ADULT;
FEMALE;
HUMANS;
LIPID METABOLISM;
MIDDLE AGED;
MUSCLE FIBERS, SKELETAL;
MUSCULAR DISEASES;
YOUNG ADULT;
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EID: 56049102118
PISSN: 00283886
EISSN: 19984022
Source Type: Journal
DOI: 10.4103/0028-3886.43460 Document Type: Article |
Times cited : (10)
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References (14)
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