Spinobulbar muscular atrophy (Kennedy's disease): A rare diagnosis in the Greek population
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference12 articles.
1. Perspectives of Kennedy's disease;Finsterer;J. Neurol. Sci.,2010
2. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy;La Spada;Nature,1991
3. Epidemiological survey of X-linked bulbar and spinal muscular atrophy, or Kennedy's disease, in the province of Reggio Emilia, Italy;Guidetti;Eur. J. Epidemiol.,2001
4. Correlation of clinical and molecular features in spinal bulbar muscular atrophy;Fratta;Neurology,2014
5. High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients;Mok;Neurobiol. Aging,2012
Cited by 2 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. Wide range of reduced penetrance alleles in spinal and bulbar muscular atrophy: a model-based approach;Journal of Medical Genetics;2020-06-22
2. Kennedy’s disease (spinal and bulbar muscular atrophy): a clinically oriented review of a rare disease;Journal of Neurology;2018-07-13
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