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Neuropathology, ISSN 0919-6544, 04/2018, Volume 38, Issue 2, pp. 113 - 124
Journal Article
Hearing Research, ISSN 0378-5955, 09/2015, Volume 327, pp. 235 - 244
Journal Article
by Peng, HR and Wang, CR and Chen, Z and Sun, ZF and Jiao, B and Li, K and Huang, FZ and Hou, X and Wang, JL and Shen, L and Xia, K and Tang, BS and Jiang, H
NEUROBIOLOGY OF AGING, ISSN 0197-4580, 09/2014, Volume 35, Issue 9, pp. 2179.e15 - 2179.e18
Polymorphism of the apolipoprotein E (APOE) gene has been defined as a modifying factor for age at onset (AO) in neurodegenerative disorders. The AO of... 
CHOLESTEROL | ALZHEIMERS-DISEASE | PHENOTYPE | SCA3/MJD | ATXN3 gene | RISK | APOE gene | NEUROSCIENCES | DOMINANT SPINOCEREBELLAR | GERIATRICS & GERONTOLOGY | OF-ONSET | GENE | Alleles | FREQUENCY | APOLIPOPROTEIN-E GENOTYPES | PARKINSON-DISEASE | Genotypes
Journal Article
by Yuan, XQ and Ou, RW and Hou, YB and Chen, XP and Cao, B and Hu, X and Shang, HF
FRONTIERS IN NEUROLOGY, ISSN 1664-2295, 02/2019, Volume 10, p. 110
Objectives: Our study attempted to systematically explore the prevalence of extra-cerebellar signs and non-motor symptoms, such as anxiety, depression,... 
DEPRESSION | SCA3 | spinocerebellar ataxia type 3 | DISORDERS | CLINICAL-FEATURES | DYSTONIA | non-motor symptoms | NEUROSCIENCES | CLINICAL NEUROLOGY | sleep disturbances | fatigue | extra-cerebellar signs | MACHADO-JOSEPH-DISEASE | RATING-SCALE | DEFICITS | DAYTIME SOMNOLENCE | SEVERITY
Journal Article
Movement Disorders, ISSN 0885-3185, 07/2009, Volume 24, Issue 9, pp. 1387 - 1390
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 10/2019, Volume 10
Background: Spinocerebellar ataxia type 3 (SCA3)/Machado-Joseph disease (MJD) is the most common type of autosomal dominant ataxia. Like other... 
Proteins | Nervous system diseases | Prognosis | Spinocerebellar ataxia | Quality control | Heat shock proteins | Development and progression | CHIP | SARA | SCA3 | serum | ICARS | cerebrospinal fluid
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 05/2010, Volume 18, Issue 5, pp. 621 - 623
Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disorder of late onset (occurring at a mean age of 40.2 years). The clinical... 
SYSTEM | CEREBELLAR | AZORES ISLANDS | SCA3 | REPEAT | MJD | BIOCHEMISTRY & MOLECULAR BIOLOGY | transcript variation | CLINICAL-FEATURES | SOMATIC MOSAICISM | polyglutamine disorders | FAMILIES | GENETICS & HEREDITY | CAG repeats
Journal Article
Journal Article