A NEW VARIANT OF LATE-ONSET MYOPHOSPHORYLASE DEFICIENCY

被引:26
作者
KOST, GJ [1 ]
VERITY, MA [1 ]
机构
[1] UNIV CALIF LOS ANGELES, DEPT NEUROPATHOL, LOS ANGELES, CA 90024 USA
关键词
D O I
10.1002/mus.880030302
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
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页码:195 / 201
页数:7
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共 58 条
[1]   METABOLIC AND CIRCULATORY RESPONSES TO MUSCULAR EXERCISE IN A SUBJECT WITH GLYCOGEN STORAGE DISEASE (MCARDLES DISEASE) [J].
ANDERSEN, KL ;
LUNDJOHA.P ;
CLAUSEN, G .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1969, 24 (02) :105-&
[2]   HISTOPATHOLOGY OF MCARDLES DISEASE IN A FAMILY [J].
BALE, P ;
HAMMETT, JF ;
NEALE, FC .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1967, 94 (02) :293-+
[3]  
BANK WJ, 1972, NEW ENGL J MED, V287, P1102
[4]  
BANK WJ, 1972, T AM NEUROL ASSOC, V97, P179
[5]  
BERGER M, 1978, FORTSCHR NEUROL PSYC, V46, P312
[6]  
BERGMEYER HU, 1963, METHODS ENZYMATIC ED, P266
[7]  
BOUDOURESQUES J, 1967, REV NEUROL-FRANCE, V117, P650
[8]   MCARDLES MYOPATHY . A REPORT OF A CASE WITH OBSERVATIONS ON MUSCLE ULTRASTRUCTURE [J].
BROWNELL, B ;
HUGHES, JT ;
GOLDBY, FS ;
WOODS, HF .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1969, 9 (03) :515-&
[9]  
CHANARD J, 1972, ARCH FR PEDIATR, V29, P505
[10]   DOMINANT INHERITANCE OF MCARDLE SYNDROME [J].
CHUI, LA ;
MUNSAT, TL .
ARCHIVES OF NEUROLOGY, 1976, 33 (09) :636-641