Identification of a Novel Mutation and Prevalence Study for Fabry Disease in Japanese Dialysis Patients-Reference-Cited by-同舟云学术

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Identification of a Novel Mutation and Prevalence Study for Fabry Disease in Japanese Dialysis Patients

Published:2012-05-08 Issue:5 Volume:34 Page:566-570
ISSN:0886-022X
Container-title:Renal Failure
language:en
Short-container-title:Renal Failure

Author:

Nishino Tomoya,Obata Yoko,Furusu Akira,Hirose Misaki,Shinzato Ken,Hattori Kiyoko,Nakamura Kimitoshi,Matsumoto Tadashi,Endo Fumio,Kohno Shigeru

Publisher

Informa UK Limited

Subject

Nephrology,Critical Care and Intensive Care Medicine,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/0886022X.2012.669300

Reference27 articles.

1. Enzymatic Defect in Fabry's Disease

2. Fabry's Disease: Classification as a Sphingolipidosis and Partial Characterization of a Novel Glycolipid

3. An Atypical Variant of Fabry's Disease in Men with Left Ventricular Hypertrophy

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1. Genetic Diagnosis of Adult Hemodialysis Patients With Unknown Etiology;Kidney International Reports;2024-04

2. A Systematic Literature Review on the Use of Dried Biofluid Microsampling in Patients With Kidney Disease;Journal of Clinical Laboratory Analysis;2024-03-25

3. Impact of GLA Variant Classification on the Estimated Prevalence of Fabry Disease: A Systematic Review and Meta-Analysis of Screening Studies;Circulation: Genomic and Precision Medicine;2023-12-04

4. Prevalence of Fabry disease in patients with chronic kidney disease: A systematic review and meta-analysis;Molecular Genetics and Metabolism;2023-12

5. Modeling of Fabry disease nephropathy using patient derived human induced pluripotent stem cells and kidney organoid system;Journal of Translational Medicine;2023-02-22

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