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Volumn 70, Issue 8, 1999, Pages 745-749

Adult polyglucosan body disease. Report of a case with predominant involvement of the central and peripheral nervous system and branching enzyme deficiency in leukocytes;Adulte polyglukosan-korperkrankheit. Fallbeispiel mit uberwiegender beteiligung des zentralen und peripheren nervensystems und branchingenzymdefekt in leukozyten

Author keywords

APBD; Branching enzyme; N.suralis biopsy

Indexed keywords

1,4 ALPHA GLUCAN BRANCHING ENZYME; GLYCOGEN;

EID: 0033174259     PISSN: 00282804     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001150050505     Document Type: Article
Times cited : (7)

References (16)
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    • Diagnosis of glycogen storage disease
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    • Adult polyglucosan body myopathy with subclinical peripheral neuropathy: Case report and review of diseases associated with polyglucosan body accumulation
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    • Immunological homogeneity of Lafora body, corpora amylacea, basophilic degeneration in heart, and intracytoplasmasmic inclusions of liver and heart in type IV glycogenosis
    • Yokota T, Ishihara T, Kawano H (1987) Immunological homogeneity of Lafora body, corpora amylacea, basophilic degeneration in heart, and intracytoplasmasmic inclusions of liver and heart in type IV glycogenosis. Acta Pathol Jpn 37:941-947
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.