Clinical and genetic study of Japanese patients with type 3 Gaucher disease-Reference-Cited by-同舟云学术

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Clinical and genetic study of Japanese patients with type 3 Gaucher disease

Published:2009-08 Issue:4 Volume:97 Page:272-277
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Tajima Asako,Yokoi Takayuki,Ariga Masamichi,Ito Takeru,Kaneshiro Eiko,Eto Yoshikatsu,Ida Hiroyuki

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference22 articles.

1. A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher’s disease;Tsuji;N. Engl. J. Med.,1987

2. Effectiveness of enzyme placement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5years of treatment: a report from the Gaucher Registry;Weinreb;Am. J. Med.,2002

3. Eight-year clinical outcomes of long-term enzyme replacement therapy for 884 children with Gaucher disease type 1;Andersson;Pediatrics,2008

4. Ten years’ experience of bone marrow transplantation for Gaucher disease;Ringden;Transplantation,1995

5. Sustained therapeutic effects of oral miglustat (Zavesca, N-butyldeoxynojirimycin, OGT 918) in type 1 Gaucher disease;Elstein;J. Inherit. Metab. Dis.,2004

Cited by 63 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. Allele frequency of pathogenic variants causing acid sphingomyelinase deficiency and Gaucher disease in the general Japanese population;Human Genome Variation;2024-06-12

2. Rapid and long‐lasting efficacy of high‐dose ambroxol therapy for neuronopathic Gaucher disease: A case report and literature review;Molecular Genetics & Genomic Medicine;2024-03-30

3. A review of type 3 Gaucher disease: unique neurological manifestations and advances in treatment;Acta Neurologica Belgica;2024-02-28

4. Gaucher Disease Types I and III Responded Well to Substrate Reduction Therapy Using Eliglustat;Internal Medicine;2023-10-15

5. Gaucher disease in a patient with membranoproliferative glomerulonephritis: case report;BMC Nephrology;2023-09-29

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