Determination of Gaucher's disease phenotypes with monoclonal antibody-Reference-Cited by-同舟云学术

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Determination of Gaucher's disease phenotypes with monoclonal antibody

Published:1983-07 Issue:3 Volume:131 Page:283-287
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Ginns Edward I.,Tegelaers Franz P.W.,Barneveld Ruud,Galjaard Hans,Reuser Arnold J.J.,Brady Roscoe O.,Tager Joseph M.,Barranger John A.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference15 articles.

1. Glucosyl ceramide lipidosis: Gaucher's disease;Brady,1983

2. Über sog. idiopathische Splenomegalie-typus Gaucher;Marchand;München Med Wschr,1907

3. Metabolism of glucocerebroside. II. Evidence of an enzymatic deficiency in Gaucher's disease;Brady;Biochem Biophys Res Commun,1965

4. Accumulation of glucosylceramide and glycosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease;Nilsson;J Neurochem,1982

5. Acid β-glucosidase and the diagnosis of Gaucher's disease in liver and spleen;Butterworth;Clin Chim Acta,1978

Cited by 51 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Processing and maturation of human glucocerebrosidase;Gaucher Disease: Basic and Clinical Perspectives;2013-08

2. Type 2 Gaucher disease: Phenotypic variation and genotypic heterogeneity;Blood Cells, Molecules, and Diseases;2011-01

3. Generation of Polyclonal Antibodies Against Recombinant Human Glucocerebrosidase Produced in Escherichia coli;Molecular Biotechnology;2010-06-24

4. Glycosphingolipid studies of visceral tissues and brain from type 1 Gaucher disease variants;Clinical Genetics;2008-04-23

5. Partial Restoration of Mutant Enzyme Homeostasis in Three Distinct Lysosomal Storage Disease Cell Lines by Altering Calcium Homeostasis;PLoS Biology;2008-02-05

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