Spinocerebellar & Related Ataxias

Spinocerebellar ataxias (SCA) are hereditary and characterized by cerebellar degeneration, which affects muscle coordination and balance. Discover the latest research on SCA and related ataxias here.

October 21, 2020

Clinical characteristics of ataxia-telangiectasia presenting dystonia as a main manifestation

Clinical Neurology and Neurosurgery
Minkyeong KimJinyoung Youn
October 13, 2020
Review
Open Access

Spatial Mechanisms for Segregation of Competing Sounds, and a Breakdown in Spatial Hearing

Frontiers in Neuroscience
John C Middlebrooks, Michael F Waters
October 8, 2020
Open Access

Cerebellar patients have intact feedback control that can be leveraged to improve reaching

ELife
Amanda M ZimmetNoah J Cowan
October 19, 2020

Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: a multicenter experience over ten years

European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies
Lu YangZhi-Ying Wu
October 16, 2020
Open Access

Ablation of polyamine catabolic enzymes provokes Purkinje cell damage, neuroinflammation, and severe ataxia

Journal of Neuroinflammation
Kamyar ZahediManoocher Soleimani
October 13, 2020
Case Report
Open Access

Facial Dysmorphism, Hirsutism, and Failure to Thrive as Manifestation of Leigh Syndrome in a Child with SURF1 Mutation

Journal of Pediatric Neurosciences
Dhinesh Baskaran, Nahin Hussain
October 6, 2020

A Novel Variant in CWF19L1 Gene in a Family with Late-Onset Autosomal Recessive Cerebellar Ataxia 17

Neurological Research
Hussein AlgahtaniMuhammad Imran Naseer
October 17, 2020
Review
Open Access

SARS-CoV-2 immunity: review and applications to phase 3 vaccine candidates

Lancet
Gregory A PolandRichard B Kennedy
October 7, 2020
Review

Assessment of Ataxia Rating Scales and Cerebellar Functional Tests: Critique and Recommendations

Movement Disorders : Official Journal of the Movement Disorder Society
Santiago Perez-Lloretand members of the MDS Rating Scales Review Committee
October 8, 2020
Open Access

Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients With Movement Disorders

Movement Disorders : Official Journal of the Movement Disorder Society
Wai Yan YauHenry Houlden
October 14, 2020
Case Report

Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences
Y HouZ X Wang
October 7, 2020

Quantitative Assessment of Friedreich Ataxia through the self-drinking activity

Annual International Conference of the IEEE Engineering in Medicine and Biology Society
Ragil KrishnaDavid J Szmulewicz
October 9, 2020

In-vivo microstructural white matter changes in early spinocerebellar ataxia 2

Acta Neurologica Scandinavica
Albert StezinPramod Kumar Pal
October 18, 2020

Safety and Efficacy of Omaveloxolone in Friedreich's Ataxia (MOXIe Study)

Annals of Neurology
David R LynchColin J Meyer
October 28, 2020

Prodromal Spinocerebellar Ataxia Type 2 Subjects Have Quantifiable Gait and Postural Sway Deficits

Movement Disorders : Official Journal of the Movement Disorder Society
Luis Velázquez-PérezChristopher M Gomez
October 26, 2020

Differential value of external anal- and urethral-sphincter electromyography in multiple system atrophy cerebellar type and spinocerebellar ataxias

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
Yan MiaoFeng Qiu
October 14, 2020
Open Access

Sexual function, intimate relationships and Friedreich ataxia

Journal of Neurology
Louise CorbenMartin Delatycki
October 22, 2020
Case Report
Open Access

Identification of a likely pathogenic structural variation in the LAMA1 gene by Bionano optical mapping

NPJ Genomic Medicine
Min ChenMinyue Dong

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