POMPES DISEASE ( DIFFUSE GLYCOGENOSIS ) WITH NEURONAL STORAGE

被引:65
作者
MANCALL, EL
APONTE, GE
BERRY, RG
机构
关键词
D O I
10.1097/00005072-196501000-00008
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:85 / +
页数:1
相关论文
共 32 条
[1]  
AGNESE PAD, 1959, ANN NY ACAD SCI, V72, P439
[2]  
BODANSKY M, 1952, BIOCHEMISTRY DISEASE
[3]  
CADDELL JL, 1962, PEDIATRICS, V29, P743
[4]  
CANTAROW A, 1962, CLINICAL BIOCHEMISTR
[5]  
CHILDS AW, 1952, PEDIATRICS, V10, P208
[6]   GLYCOGEN DISEASE RESEMBLING MONGOLISM, CRETINISM, AND AMYTONIA CONGENITA - CASE REPORT AND REVIEW OF LITERATURE [J].
CLEMENT, DH ;
GODMAN, GC .
JOURNAL OF PEDIATRICS, 1950, 36 (01) :11-30
[7]  
CROME J, 1963, PSYCHIATRY, V26, P422
[8]   LATE-ONSET TYPE OF SKELETAL-MUSCLE PHOSPHORYLASE DEFICIENCY - A NEW FAMILIAL VARIETY WITH COMPLETELY AND PARTIALLY AFFECTED SUBJECTS [J].
ENGEL, WK ;
WILLIAMS, HE ;
EYERMAN, EL .
NEW ENGLAND JOURNAL OF MEDICINE, 1963, 268 (03) :135-&
[9]  
ESSER M, 1937, SCHWEIZ MED WCHNSCHR, V67, P970
[10]  
FIELD RA, 1960, METABOLIC BASIS INHE, pCH6