学术探索
学术期刊
新闻热点
数据分析
智能评审

ARTHROGRYPOSIS MULTIPLEX DUE TO CONGENITAL MUSCULAR DYSTROPHY

被引：141
作者：
BANKER, BQ
VICTOR, M
ADAMS, RD
机构：
来源：
BRAIN | 1957年 / 80卷 / 03期
关键词：
D O I：
10.1093/brain/80.3.319
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：319 / &
相关论文
共 31 条
[1]  
ADAMS RD, 1953, DISEASES MUSCLE
[2]  
Batten FE, 1911, BRAIN, V33, P433
[3]   A case of congenital spinal muscular atrophy (Family type), and a case of h ae morrhage into the spinal cord at birth, giving similar symptoms. [J].
Beevor, CE .
BRAIN, 1902, 25 :85-108
[4]  
BRANDT S, 1947, Acta Paediatr, V34, P365, DOI 10.1111/j.1651-2227.1947.tb03712.x
[5]  
BRANDT S, 1950, WERDNIGHOFFMANNS INF
[6]   The pathological examination of two cases of Amyotonia congenita with the clinical description of a fresh case. [J].
Collier, J ;
Holmes, G .
BRAIN, 1909, 32 :269-284
[7]  
Councilman WT, 1911, AM J DIS CHILD, V2, P340
[8]  
DELANGE C, 1937, ACTA PAEDIAT STOC S3, V20
[9]   AMYOPLASIA CONGENITA [J].
GILMOUR, JR .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1946, 58 (04) :675-&
[10]   Muscular shortening and dystrophy - A heredofamilial disease [J].
Hauptmann, A ;
Thannhauser, SJ .
ARCHIVES OF NEUROLOGY AND PSYCHIATRY, 1941, 46 (04) :654-664
1234