ANALYTICAL STUDY OF FABRYS-DISEASE

被引:7
作者
ROTH, J [1 ]
SCHULZE, E [1 ]
RAABE, G [1 ]
WALDMANN, G [1 ]
机构
[1] FRIEDRICH SCHILLER UNIV,PATHOL INST,ZIEGELMUHLENWEG 1,DDR-6900 JENA,EAST GERMANY
来源
VIRCHOWS ARCHIV ABTEILUNG A PATHOLOGISCHE ANATOMIE | 1974年 / 363卷 / 03期
关键词
D O I
10.1007/BF00432808
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
引用
收藏
页码:287 / 301
页数:15
相关论文
共 57 条
[1]  
Anderson W., 1898, BRIT J DERMATOL, V10, P113, DOI [10.1111/j.1365-2133.1898.tb16317.x, DOI 10.1111/J.1365-2133.1898.TB16317.X]
[2]   FABRYS DISEASE AS AN ALPHA-GALACTOSIDOSIS - EVIDENCE FOR AN ALPHA-CONFIGURATION IN TRIHEXOSYL CERAMIDE [J].
BENSAUDE, I ;
CALLAHAN, J ;
PHILIPPART, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1971, 43 (04) :913-+
[3]  
BEUTLER E, 1972, AM J HUM GENET, V24, P237
[4]   ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY [J].
BRADY, RO ;
GAL, AE ;
BRADLEY, RM ;
MARTENSS.E ;
WARSHAW, AL ;
LASTER, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1967, 276 (21) :1163-&
[5]   FABRYS DISEASE - ANTENATAL DETECTION [J].
BRADY, RO ;
UHLENDORF, BW ;
JACOBSON, CB .
SCIENCE, 1971, 172 (3979) :174-+
[6]   REPLACEMENT THERAPY FOR INHERITED ENZYME DEFICIENCY - USE OF PURIFIED CERAMIDETRIHEXOSIDASE IN FABRYS-DISEASE [J].
BRADY, RO ;
TALLMAN, JF ;
JOHNSON, WG ;
GAL, AE ;
LEAHY, WR ;
QUIRK, JM ;
DEKABAN, AS .
NEW ENGLAND JOURNAL OF MEDICINE, 1973, 289 (01) :9-14
[7]   DIE DUNNSCHICHTCHROMATOGRAPHIE VON GEWEBSSCHNITTEN [J].
BREITENE.L ;
HOLCZABE.W .
HISTOCHEMIE, 1966, 7 (04) :291-&
[8]  
CANLETT R, 1967, ANN ANAT PATH, V12, P49
[9]  
CHRISTENSEN LHO, 1966, ACTA PATHOL MIC SC, V68, P332
[10]   CERAMIDE TRIHEXOSIDOSIS (FABRYS DISEASE) WITHOUT SKIN LESIONS [J].
CLARKE, JTR ;
KNAACK, J ;
CRAWHALL, JC ;
WOLFE, LS .
NEW ENGLAND JOURNAL OF MEDICINE, 1971, 284 (05) :233-&