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amyotrophic lateral sclerosis (26) 26
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dystonic syndrome starting with focal signs or with functional dystonia (26) 26
progressive encephalomyelitis with rigidity and myoclonus (26) 26
progressive supranuclear palsy, presenting with parkinsonism (26) 26
repeat (26) 26
sca2 expansion, resulting in typical pd (26) 26
use of dat spect, facilitating differential diagnosis in patients with isolated tremor symptoms (26) 26
wilson's disease, autosomal recessive disorder linking to mutation of atp7b gene mapped to chromosome 13 (26) 26
constipation and smell loss, non-motor symptoms occurring in de novo pd patients (25) 25
fluid-attenuated inversion recovery (25) 25
urinary urgency and erectile dysfunction - common in msa (25) 25
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Movement Disorders, ISSN 0885-3185, 11/2004, Volume 19, Issue 11, pp. 1320 - 1325
Extrapyramidal features may occur in spinocerebellar ataxias consistent with neuropathological evidence of nigrostriatal involvement. Recently, striatal... 
dopamine | SPECT | SCA2 | ADCA | Dopamine
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2016, Volume 51, pp. 178.e1 - 178.e9
Journal Article
Infection and Immunity, ISSN 0019-9567, 06/2018, Volume 86, Issue 6
The Gram-negative obligate intracellular bacterium is an emerging tick-borne human pathogen. Recently, Sca2 and RickA have been implicated in adherence and... 
Rickettsia parkeri | RickA | Sca2 | Amblyomma maculatum | Actin-based motility
Journal Article
Genes, ISSN 2073-4425, 06/2017, Volume 8, Issue 6, pp. 2 - 21
RNA-binding proteins play fundamental roles in the regulation of molecular processes critical to cellular and organismal homeostasis. Recent studies have... 
ALS | RNA-DNA hybrids | Stress granules | SCA2 | RNA metabolism | PAS KINASE | DROSOPHILA HOMOLOG | POLYQ EXPANSIONS | POLY(A)-BINDING PROTEIN | LENGTH POLYGLUTAMINE EXPANSIONS | CAENORHABDITIS-ELEGANS | GENETICS & HEREDITY | stress granules | TYPE-2 SCA2 | INTRANUCLEAR INCLUSIONS | HEXANUCLEOTIDE REPEAT
Journal Article
Nature, ISSN 0028-0836, 04/2017, Volume 544, Issue 7650, pp. 362 - 366
Journal Article
Neurology Asia, ISSN 1823-6138, 12/2018, Volume 23, Issue 4, pp. 361 - 362
Spinocerebellar ataxia type 2 (SCA2) is an expanded CAG repeat disorder in ATXN2 gene with a wide range of clinical phenotypes. Chorea has been reported as one... 
Chorea | SCA2 | Korea | REPEAT | PHENOTYPE | CLINICAL NEUROLOGY | FEATURES
Journal Article
Movement Disorders, ISSN 0885-3185, 05/2017, Volume 32, Issue 5, pp. 708 - 718
Journal Article
JAMA Neurology, ISSN 2168-6149, 08/2018, Volume 75, Issue 8, pp. 1025 - 1027
This case report describes autopsy findings of progressive supranuclear palsy in a patient with a misdiagnosis of multiple system atrophy with predominant... 
CLINICAL NEUROLOGY | SCA2 | Online First | Research | Letters | Research Letter
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 01/2019, Volume 73, pp. 231.e7 - 231.e9
Common genetic risk factors are associated with frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Intermediate repeat expansions at the... 
Frontotemporal lobar degeneration | ATXN2 | polyQ repeats | SCA2 | Intermediate expansions | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | Medical research | Neurosciences | Medical genetics | Medicine, Experimental | Genetic aspects | Risk factors | Dementia
Journal Article
The Cerebellum, ISSN 1473-4222, 10/2014, Volume 13, Issue 5, pp. 568 - 579
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 8/2011, Volume 20, Issue 16, pp. 3207 - 3212
Journal Article
16.