Hearing loss in fabry disease: A 16 year follow-up study of the Danish nationwide cohort-Reference-Cited by-同舟云学术

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Hearing loss in fabry disease: A 16 year follow-up study of the Danish nationwide cohort

Published:2022-06 Issue: Volume:31 Page:100841
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Yazdanfard Puriya Daniel Würtz,Effraimidis Grigoris,Madsen Christoffer Valdorff,Nielsen Lars Holme,Rasmussen Åse Krogh,Petersen Jørgen Holm,Sørensen Søren Schwartz,Køber Lars,de Abreu Vitor Hugo Fraga,Larsen Vibeke Andrée,Feldt-Rasmussen Ulla

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference34 articles.

1. α-Galactosidase A deficiency: fabry disease;Desnick,2013

2. Gastrointestinal manifestations of Fabry disease;Keshav,2006

3. Anderson-fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males;Macdermot;J. Med. Genet.,2001

4. X-chromosome inactivation in female patients with fabry disease;Echevarria;Clin. Genet.,2016

5. The hearing status in 12 female and 15 male japanese fabry patients;Sakurai;Auris Nasus Larynx,2009

Cited by 3 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. Neurootologische Manifestationen bei Morbus Fabry – eine retrospektive Analyse;HNO;2023-09-25

2. Clinical Diagnosis and Treatment Progress of Fabry Disease;Advances in Clinical Medicine;2023

3. Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry;Orphanet Journal of Rare Diseases;2022-06-20

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