Auditory Characteristics in Patients With Mucopolysaccharidosis-Reference-Cited by-同舟云学术

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Auditory Characteristics in Patients With Mucopolysaccharidosis

Published:2019-12 Issue:10 Volume:40 Page:e955-e961
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Ahn Jungmin,Lee Jung Joo,Park Song-I.,Cho Sung-Yoon,Jin Dong-Kyu,Cho Yang-Sun,Chung Won-Ho,Hong Sung-Hwa,Moon Il Joon

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference14 articles.

1. The impact of laronidase treatment in otolaryngological manifestations of patients with mucopolysaccharidosis;Dualibi;Braz J Otorhinolaryngol,2016

2. The first 5years of clinical experience with laronidase enzyme replacement therapy for mucopolysaccharidosis I;Wraith;Expert Opin Pharmacother,2005

3. Assessment of hearing loss by pure-tone audiometry in patients with mucopolysaccharidoses;Lin;Mol Genet Metab,2014

4. Role of the pediatric otolaryngologist in diagnosis and management of children with mucopolysaccharidoses;Wold;Int J Pediatr Otorhinolaryngol,2010

5. Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004;Lin;Am J Med Genet A,2009

Cited by 9 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. Health service utilization, economic burden and quality of life of patients with mucopolysaccharidosis in China;Orphanet Journal of Rare Diseases;2024-09-06

2. Study of the peripheral and central auditory pathways in patients with mucopolysaccharidosis;Journal of Communication Disorders;2024-01

3. Hearing loss in mucopolysaccharidosis I–H (Hurler syndrome), a temporal bone report and systematic review;Otolaryngology Case Reports;2022-11

4. Hearing loss in inherited metabolic disorders: A systematic review;Metabolism;2021-09

5. Prevalence of patients with lysosomal storage disorders and peroxisomal disorders: A nationwide survey in Japan;Molecular Genetics and Metabolism;2021-07

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