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Gaucher disease: A prototype for molecular medicine

被引：23
作者：
Grabowski, GA
Saal, HM
Wenstrup, RJ
Barton, NW
机构：
[1] UNIV CINCINNATI, COLL MED, DEPT PEDIAT, CINCINNATI, OH USA
[2] UNIV CINCINNATI, COLL MED, DEPT MOLEC GENET BIOCHEM & MICROBIOL, CINCINNATI, OH USA
[3] NINCDS, NIH,DEV & METAB NEUROL BRANCH,CLIN INVEST SECT, DEV & METAB NEUROL BRANCH, BETHESDA, MD 20892 USA
来源：
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY | 1996年 / 23卷 / 01期
关键词：
D O I：
10.1016/1040-8428(96)00199-0
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
[No abstract available]
引用
收藏
页码：25 / 55
页数：31
相关论文
共 314 条
[81]   ENZYME AUGMENTATION IN MODERATE TO LIFE-THREATENING GAUCHER DISEASE [J].
FALLET, S ;
GRACE, ME ;
SIBILLE, A ;
MENDELSON, DS ;
SHAPIRO, RS ;
HERMANN, G ;
GRABOWSKI, GA .
PEDIATRIC RESEARCH, 1992, 31 (05) :496-502
[82]   COMBINED PORTAL AND VENA-CAVAL HYPERTENSION IN GAUCHER DISEASE - VALUE OF PREOPERATIVE VENOGRAPHY [J].
FELLOWS, KE ;
GRAND, RJ ;
COLODNY, AH ;
ORSINI, EN ;
CROCKER, AC .
JOURNAL OF PEDIATRICS, 1975, 87 (05) :739-743
[83]   A LESS COSTLY REGIMEN OF ALGLUCERASE TO TREAT GAUCHERS-DISEASE [J].
FIGUEROA, ML ;
ROSENBLOOM, BE ;
KAY, AC ;
GARVER, P ;
THURSTON, DW ;
KOZIOL, JA ;
GELBART, T ;
BEUTLER, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (23) :1632-1636
[84]   CORRECTION OF GLUCOCEREBROSIDASE DEFICIENCY AFTER RETROVIRAL-MEDIATED GENE-TRANSFER INTO HEMATOPOIETIC PROGENITOR CELLS FROM PATIENTS WITH GAUCHER DISEASE [J].
FINK, JK ;
CORRELL, PH ;
PERRY, LK ;
BRADY, RO ;
KARLSSON, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (06) :2334-2338
[85]  
FIRON N, 1990, AM J HUM GENET, V46, P527
[86]  
FLANAGAN AM, 1987, OSTEOPOROSIS, V2, P776
[87]  
FREDERICKSON DS, 1978, METABOLIC BASIS INHE, P730
[88]   LIPID COMPOSITION OF BRAIN IN INFANTILE GAUCHERS DISEASE [J].
FRENCH, JH ;
BROTZ, M ;
POSER, CM .
NEUROLOGY, 1969, 19 (01) :81-&
[89]  
FUJIBAYASHI S, 1985, AM J HUM GENET, V37, P741
[90]  
FUJIBAYASHI S, 1986, BIOCHIM BIOPHYS ACTA, V875, P554
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