ADULT MYOPATHY FROM GLYCOGEN STORAGE DISEASE DUE TO ACID MALTASE DEFICIENCY

被引：127

作者：

HUDGSON, P

GARDNERM.D

WORSFOLD, M

PENNINGTON, RJ

WALTON, JN

机构：

来源：

BRAIN | 1968年 / 91卷

关键词：

D O I：

10.1093/brain/91.3.435

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：435 / +

页数：1

共 55 条

[1] CONGENITAL NONPROGRESSIVE MYOPATHY - CENTRAL CORE DISEASE AND NEMALINE MYOPTAHY IN 1 FAMILY [J].

AFIFI, AK ;

SMITH, JW ;

ZELLWEGER, H .

NEUROLOGY, 1965, 15 (04) :371-+

[2]

AGUAYO AJ, IN PRESS

[3]

BERGMEYER HU, 1963, METHODS ENZYMATIC ED, P266

[4]

BOURNE GH, 1963, MUSCULAR DYSTROPH ED, P193

[5]

BOURNE GH, 1963, MUSCULAR DYSTROPH ED, P159

[6] ALPHA-1,4-GLUCOSIDASE ACTIVITY IN LEUCOCYTES FROM FAMILY OF 2 BROTHERS WHO LACK THIS ENZYME IN MUSCLE [J].

BROWN, BI ;

ZELLWEGER, H .

BIOCHEMICAL JOURNAL, 1966, 101 (01) :C16-+

[7]

BUCHTHAL F, 1963, MUSCULAR DYSTROPHY M, P193

[8]

CARDIFF RD, 1966, PEDIATRICS, V37, P249

[9] GLYCOGEN DISEASE RESEMBLING MONGOLISM, CRETINISM, AND AMYTONIA CONGENITA - CASE REPORT AND REVIEW OF LITERATURE [J].

CLEMENT, DH ;

GODMAN, GC .

JOURNAL OF PEDIATRICS, 1950, 36 (01) :11-30

[10]

CORI GT, 1953, HARVEY LECT, V48, P145

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