Oculopharyngeal muscular dystrophy with frontotemporal dementia
Author:
Publisher
Elsevier BV
Subject
Geriatrics and Gerontology,Gerontology
Reference9 articles.
1. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat Genet,1998
2. Oculopharyngeal muscular dystrophy associated with dementia;Mizoi;Intern Med,2011
3. An 18 alanine repeat in a severe form of oculopharyngeal muscular dystrophy;Jouan;Can J Neurol Sci,2014
4. Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophy;Dubbioso;J Neurol,2012
5. Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes;Blumen;Neurology,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. Behavioural Impairment and Frontotemporal Dementia in Oculopharyngeal Muscular Dystrophy;Journal of Neuromuscular Diseases;2022-01-04
2. Oculopharyngeal muscular dystrophy (OPMD) and dementia in a 75-year-old female;BMJ Case Reports;2019-09
3. A Preliminary Videofluoroscopic Investigation of Swallowing Physiology and Function in Individuals with Oculopharyngeal Muscular Dystrophy (OPMD);Dysphagia;2018-05-03
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