Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease-Reference-Cited by-同舟云学术

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Clinical utility of urinary mulberry bodies/cells testing in the diagnosis of Fabry disease

Published:2023-09 Issue: Volume:36 Page:100983
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Nakamura Katsuya,Mukai Saki,Takezawa Yuka,Natori Yuika,Miyazaki Akari,Ide Yuichiro,Takebuchi Mayu,Nanato Kana,Katoh Mizuki,Suzuki Harue,Sakyu Akiko,Kojima Tomomi,Kise Emiko,Hanafusa Hiroaki,Kosho Tomoki,Kuwahara Koichiro,Sekijima Yoshiki

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference23 articles.

1. An atypical variant of Fabry’s disease in men with left ventricular hypertrophy;Nakao;N. Engl. J. Med.,1995

2. Fabry disease: detection of undiagnosed hemodialysis patients and identification of a “renal variant” phenotype;Nakao;Kidney Int.,2003

3. Safety and efficacy of recombinant human α-galactosidase A replacement therapy in Fabry’s disease;Eng;N. Engl. J. Med.,2001

4. Enzyme replacement therapy in Fabry disease;Schiffmann;JAMA.,2001

Cited by 2 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. Genetic counselling for at-risk family members with hereditary transthyretin amyloidosis: data from a single-centre study;Amyloid;2024-05-25

2. Effects of switching from agalsidase−α to agalsidase−β on biomarkers, renal and cardiac parameters, and disease severity in fabry disease forming neutralizing antidrug antibodies: a case report;CEN Case Reports;2023-12-22

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