PRENATAL-DIAGNOSIS OF CANAVAN DISEASE

被引:24
作者
MATALON, R [1 ]
MICHALS, K [1 ]
GASHKOFF, P [1 ]
KAUL, R [1 ]
机构
[1] UNIV ILLINOIS,DEPT NUTR & MED DIETET,CHICAGO,IL 60680
关键词
D O I
10.1007/BF02435985
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:392 / 394
页数:3
相关论文
共 8 条
[1]   Schilder's encephalitis periaxialis diffusa - Report or a case in a child aged sixteen and one-half months [J].
Canavan, MM .
ARCHIVES OF NEUROLOGY AND PSYCHIATRY, 1931, 25 (02) :299-308
[2]  
GOODMAN SI, 1981, DIAGNOSIS ORGANIC AC, P3
[3]   N-ACETYLASPARTIC ACIDURIA DUE TO ASPARTOACYLASE DEFICIENCY - A NEW ETIOLOGY OF CHILDHOOD LEUKODYSTROPHY [J].
HAGENFELDT, L ;
BOLLGREN, I ;
VENIZELOS, N .
JOURNAL OF INHERITED METABOLIC DISEASE, 1987, 10 (02) :135-141
[4]   PURIFICATION, CHARACTERIZATION, AND LOCALIZATION OF ASPARTOACYLASE FROM BOVINE BRAIN [J].
KAUL, R ;
CASANOVA, J ;
JOHNSON, AB ;
TANG, P ;
MATALON, R .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (01) :129-135
[5]   ASPARTOACYLASE DEFICIENCY - THE ENZYME DEFECT IN CANAVAN DISEASE [J].
MATALON, R ;
KAUL, R ;
CASANOVA, J ;
MICHALS, K ;
JOHNSON, A ;
RAPIN, I ;
GASHKOFF, P ;
DEANCHING, M .
JOURNAL OF INHERITED METABOLIC DISEASE, 1989, 12 :329-331
[6]   ASPARTOACYLASE DEFICIENCY AND N-ACETYLASPARTIC ACIDURIA IN PATIENTS WITH CANAVAN DISEASE [J].
MATALON, R ;
MICHALS, K ;
SEBESTA, D ;
DEANCHING, M ;
GASHKOFF, P ;
CASANOVA, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 29 (02) :463-471
[7]  
RIORDAN JF, 1967, METHOD ENZYMOL, V11, P565
[8]  
VANBOGAERT L, 1967, SPONGY DEGENERATION, P3