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Hypergonadotropic hypogonadism, progressive early-onset spinocerebellar ataxia, and late-onset sensorineural hearing loss: case report and literature review.Fatty Acid Oxidation and Cardiovascular Risk during Menopause: A Mitochondrial Connection?Rhabdomyolysis: a genetic perspective.Endocrine manifestations related to inherited metabolic diseases in adults.Acquired multiple acyl-CoA dehydrogenase deficiency and marked selenium deficiency causing severe rhabdomyolysis in a horse.Lipid storage myopathy with clinical markers of Marfan syndrome: A rare associationTherapeutic advances in the management of Pompe disease and other metabolic myopathiesRhabdomyolysis. The role of diagnostic and prognostic factors.Rhabdomyolysis as a manifestation of a metabolic disease: a case reportA Nonsense Variant in the ACADVL Gene in German Hunting Terrier Dogs with Exercise Induced Metabolic Myopathy.
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
State of the art in muscle lipid diseases.
@ast
State of the art in muscle lipid diseases.
@en
State of the art in muscle lipid diseases.
@nl
type
label
State of the art in muscle lipid diseases.
@ast
State of the art in muscle lipid diseases.
@en
State of the art in muscle lipid diseases.
@nl
prefLabel
State of the art in muscle lipid diseases.
@ast
State of the art in muscle lipid diseases.
@en
State of the art in muscle lipid diseases.
@nl
P2860
P1433
P1476
State of the art in muscle lipid diseases.
@en
P2093
P2860
P304
P5008
P577
2010-10-01T00:00:00Z