Immunoquantification of β-glucosidase:: Diagnosis and prediction of severity in Gaucher disease.

被引:7
作者
Fuller, M
Lovejoy, M
Hopwood, JJ
Meikle, PJ
机构
[1] Youth & Womens Hlth Serv, Dept Genet Med Children, Lysosomal Dis Res Unit, Adelaide, SA 5006, Australia
[2] Univ Adelaide, Dept Pediat, Adelaide, SA, Australia
关键词
D O I
10.1373/clinchem.2005.053538
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
[No abstract available]
引用
收藏
页码:2200 / 2202
页数:3
相关论文
共 17 条
[11]   SAPOSIN PROTEINS - STRUCTURE, FUNCTION, AND ROLE IN HUMAN LYSOSOMAL STORAGE DISORDERS [J].
OBRIEN, JS ;
KISHIMOTO, Y .
FASEB JOURNAL, 1991, 5 (03) :301-308
[12]  
SIBILLE A, 1993, AM J HUM GENET, V52, P1094
[13]  
THEOPHILUS B, 1989, AM J HUM GENET, V45, P212
[14]  
Umapathysivam K, 2000, CLIN CHEM, V46, P1318
[15]   Management of neuronopathic Gaucher disease: A European consensus [J].
Vellodi, A ;
Bembi, B ;
de Villemeur, TB ;
Collin-Histed, T ;
Erikson, A ;
Mengel, E ;
Rolfs, A ;
Tylki-Szymanska, A .
JOURNAL OF INHERITED METABOLIC DISEASE, 2001, 24 (03) :319-327
[16]   Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: A report from the Gaucher Registry [J].
Weinreb, NJ ;
Charrow, J ;
Andersson, HC ;
Kaplan, P ;
Kolodny, EH ;
Mistry, P ;
Pastores, G ;
Rosenbloom, BE ;
Scott, CR ;
Wappner, RS ;
Zimran, A .
AMERICAN JOURNAL OF MEDICINE, 2002, 113 (02) :112-119
[17]  
ZOLA H, 1982, MONOCLONAL HYBRIDOMA, P1