Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1)-Reference-Cited by-同舟云学术

Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1)

Published:2020-09-24 Issue:1 Volume:42 Page:18-23
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:

Author:

Frezza Erica,Fuccillo Emanuela,Petrucci Antonio,Greco Giulia,Nucera Gabriele,Bruno Ernesto,Giardina Emiliano,Tupler Rossella,Di Mauro Roberta,Di Girolamo Stefano,Massa Roberto

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Sensory Systems,Otorhinolaryngology

Reference25 articles.

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2. Genetic and epigenetic contributors to FSHD;Daxinger;Curr Opin Genet Dev,2015

3. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2;Lemmers;Nat Genet,2012

4. Clinical features of facioscapulohumeral muscular dystrophy 2;De Greef;Neurology,2010

5. Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine;Tawil;Neurology,2015

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1. Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy;Frontiers in Genome Editing;2022-07-15

2. Systemic manifestations and symptom burden of facioscapulohumeral muscular dystrophy in a referral cohort;Muscle & Nerve;2022-01-25

3. Auditory Dysfunction in Facioscapulohumeral Muscular Dystrophy Type 1;Otology & Neurotology;2021-11-11

4. Response To Letter To The Editor “Auditory Dysfunction In Facioscapulohumeral Muscular Dystrophy Type 1;Otology & Neurotology;2021-11-11