LIPID STORAGE MYOPATHY - RECOGNIZABLE CLINICOPATHOLOGICAL ENTITY

被引：18

作者：

JOHNSON, MA

FULTHORPE, JJ

HUDGSON, P

机构：

[1] NEWCASTLE GEN HOSP, MUSCULAR DYSTROPHY RES LABS, DEPT EXPTL NEUROPATHOL, NEWCASTLE NE4 6BE, ENGLAND

[2] ROY VICTORIA INFIRM, DEPT NEUROL, NEWCASTLE, ENGLAND

来源：

ACTA NEUROPATHOLOGICA | 1973年 / 24卷 / 02期

关键词：

D O I：

10.1007/BF00684832

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：97 / 106

页数：10

共 12 条

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[4]

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[7] A SKELETAL-MUSCLE DISORDER ASSOCIATED WITH INTERMITTENT SYMPTOMS AND A POSSIBLE DEFECT OF LIPID METABOLISM [J].

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LEVY, RI .

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[8] ARE ACTIVE AND INACTIVE PHOSPHORYLASES HISTOCHEMICALLY DISTINGUISHABLE [J].

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[9] AN IMPROVED METHOD OF FIXATION FOR FORMALIN-SENSITIVE ENZYMES WITH SPECIAL REFERENCE TO MYOSIN ADENOSINE TRIPHOSPHATASE [J].

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[10]

HUDGSON P, 1972, J NEUROL SCI, V16, P343, DOI 10.1016/0022-510X(72)90197-9

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