Polyglycosan body myopathy;Spätmanifestation einer polyglykosankörpermyopathie

Nervenarzt

Volumn 77, Issue 12, 2006, Pages 1487-1491

  Jeub, M ^a   Kappes Horn, K ^a   Kornblum, C ^a   Fischer, D ^a,b  

^a UNIVERSITY OF BONN   (Germany)

^b Kantonspital St Gallen ^*  (Switzerland)

Author keywords

Acid maltase deficiency; Branching enzyme deficiency; Debranching enzyme deficiency; Glycogenosis; Polyglycosan body disease

Indexed keywords

AGED; ARTICLE; CASE REPORT; ELECTROPHYSIOLOGY; FEMALE; HISTOPATHOLOGY; HUMAN; MALE; MYOPATHY; POLYGLYCOSAN BODY MYOPATHY;

1,4-ALPHA-GLUCAN BRANCHING ENZYME; AGED; BIOPSY; DIAGNOSIS, DIFFERENTIAL; FEMALE; GLYCOGEN DEBRANCHING ENZYME SYSTEM; GLYCOGEN STORAGE DISEASE TYPE III; GLYCOGEN STORAGE DISEASE TYPE IV; HUMANS; MALE; MUSCLE, SKELETAL; MYOSITIS, INCLUSION BODY; VACUOLES;

EID: 33845632034     PISSN: 00282804     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00115-006-2184-x     Document Type: Article

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