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Volumn 30, Issue 5, 1988, Pages 667-672

Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy

Author keywords

[No Author keywords available]

Indexed keywords

GLUTAMIC ACID;

EID: 0023813321     PISSN: 00121622     EISSN: 14698749     Source Type: Journal    
DOI: 10.1111/j.1469-8749.1988.tb04806.x     Document Type: Article
Times cited : (13)

References (31)
  • 11
    • 0018924628 scopus 로고
    • Multiple acyl‐CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein
    • (1980) Pediatric Research , vol.14 , pp. 12-17
    • McCabe, E.R.B.1    Fennessey, P.V.2    Mace, J.W.3
  • 31
    • 0343259326 scopus 로고
    • Assay of acyl‐CoA dehydrogenase in muscle and liver and identification of four new cases of medium‐chain acyl‐CoA dehydrogenase deficiency associated with systemic carnitine deficiency
    • (1986) Muscle and Nerve , pp. 193
    • Zierz, S.1    Engel, A.G.2    Romsche, C.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.