TYPE I FIBER HYPOTROPHY AND CENTRAL NUCLEI - A RARE CONGENITAL MUSCLE ABNORMALITY WITH A POSSIBLE EXPERIMENTAL MODEL

被引：152

作者：

ENGEL, WK

GOLD, GN

KARPATI, G

机构：

[1] Medical Neurology Branch, National Institutes of Health, Bethesda, Muscular Dystrophy Association of Canada, Bethesda, Md

来源：

关键词：

D O I：

10.1001/archneur.1968.00470340121011

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：435 / &

共 30 条

[1] BANKER B, 1967, J NEUROPATH EXP NEUR, V26, P133
[2] ARTHROGRYPOSIS MULTIPLEX DUE TO CONGENITAL MUSCULAR DYSTROPHY
BANKER, BQ
VICTOR, M
ADAMS, RD
[J]. BRAIN, 1957, 80 (03) : 319 - &
[3] Bruce A, 1901, TOPOGRAPHICAL ATLAS
[4] COLEMAN RF, 1967, LAB INVEST, V16, P647
[5] Councilman WT, 1911, AM J DIS CHILD, V2, P340
[6] DEHAAN, 1965, ORGANOGENESIS ED, P337
[7] DREWS GA, 1967, NATURE, V212, P1551
[8] ENZYME HISTOCHEMISTRY OF SKELETAL MUSCLE .3. NEUROGENIC MUSCULAR ATROPHIES
DUBOWITZ, V
[J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1966, 29 (01) : 23 - &
[9] ESSENTIALITY OF HISTO- AND CYTOCHEMICAL STUDIES OF SKELETAL MUSCLE IN INVESTIGATION OF NEUROMUSCULAR DISEASE
ENGEL, WK
[J]. NEUROLOGY, 1962, 12 (11) : 778 - +
[10] ENGEL WK, 1967, PEDIATR CLIN N AM, V14, P963