SARCOTUBULAR MYOPATHY - NEWLY RECOGNIZED, BENIGN, CONGENITAL, FAMILIAL MUSCLE DISEASE

被引：33

作者：

JERUSALEM, F

ENGEL, AG

GOMEZ, MR

机构：

[1] MAYO CLIN & MAYO FDN, DEPT NEUROL, ROCHESTER, MN 55901 USA

[2] MAYO CLIN & MAYO FDN, NEUROMUSCULAR RES LAB, ROCHESTER, MN 55901 USA

来源：

NEUROLOGY | 1973年 / 23卷 / 09期

关键词：

D O I：

10.1212/WNL.23.9.897

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：897 / 906

页数：10

共 18 条

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[2] REDUCING BODY MYOPATHY [J].

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NEVILLE, HE .

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[3] FAMILIAL MYOPATHY WITH PROBABLE LYSIS OF MYOFIBRILS IN TYPE-I FIBERS [J].

CANCILLA, PA ;

KALYANARAMAN, K ;

VERITY, MA ;

MUNSAT, T ;

PEARSON, CM .

NEUROLOGY, 1971, 21 (06) :579-+

[4]

ENGEL AG, 1971, MAYO CLIN PROC, V46, P666

[5]

ENGEL AG, 1970, MAYO CLIN PROC, V45, P774

[6] ACID MALTASE DEFICIENCY IN ADULTS - STUDIES IN 4 CASES OF A SYNDROME WHICH MAY MIMIC MUSCULAR DYSTROPHY OR OTHER MYOPATHIES [J].

ENGEL, AG .

BRAIN, 1970, 93 :599-+

[7]

ENGEL AG, 1972, MAYO CLIN PROC, V47, P377

[8]

ENGEL AG, 1968, MAYO CLIN PROC, V43, P233

[9]

ENGEL AG, 1970, EXCERPTA MEDICA 199, P71

[10]

ENGEL AG, PATHOLOGIC PHYSIOLOG

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