Literature DB >> 23848287

Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testing.

Aurore Mensah1, Nanna Witting, Morten Duno, Dan Milea, John Vissing.   

Abstract

Entities:  

Mesh:

Year:  2013        PMID: 23848287     DOI: 10.1111/aos.12243

Source DB:  PubMed          Journal:  Acta Ophthalmol        ISSN: 1755-375X            Impact factor:   3.761


× No keyword cloud information.
  3 in total

1.  Analysis of Molecular Genetic Testing Referrals for Inherited Retinal Dystrophies in a Quebec Tertiary Care Center Over a Decade.

Authors:  Alexandre Lachance; Mélanie Hébert; Marc Hébert; Christian Salesse; Serge Bourgault; Ali Dirani
Journal:  Clin Ophthalmol       Date:  2022-02-02

2.  Oculopharyngeal muscular dystrophy misdiagnosed as myasthenia gravis: Case report and review of literature.

Authors:  Omid Aryani; Mohammadreza Akbari; Masoud Aghsaei-Fard; Arash Mirmohammad-Sadeghi; Samira Yadegari
Journal:  Iran J Neurol       Date:  2017-04-04

Review 3.  Recent Progress in Oculopharyngeal Muscular Dystrophy.

Authors:  Satoshi Yamashita
Journal:  J Clin Med       Date:  2021-03-29       Impact factor: 4.241

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.