Pathomechanism characterization and potential therapeutics identification for SCA3 targeting neuroinflammation

Chiu YJ, Lin SA, Chen WL, Lin TH, Lin CH, Yao CF, Lin W, Wu YR, Chang KH, Lee-Chen GJ, Chen CM.

Aging (Albany NY). 2020 Nov 10;12. doi: 10.18632/aging.103700. Online ahead of print.

Paraneoplastic myeloneuropathies: Clinical, oncologic and serologic accompaniments

Shah S, Do Campo RV, Kumar N, McKeon A, Flanagan EP, Klein C, Pittock SJ, Dubey D.

Neurology. 2020 Nov 18:10.1212/WNL.0000000000011218. doi: 10.1212/WNL.0000000000011218. Online ahead of print.

Vocal Fold "Paralysis": An Early Sign in Multiple System Atrophy

Tipton PW, Ekbom DC, Rutt AL, van Gerpen JA.

J Voice. 2020 Nov;34(6):940-944. doi: 10.1016/j.jvoice.2019.06.008. Epub 2019 Jul 16.

The Use of New Mobile and Gaming Technologies for the Assessment and Rehabilitation of People with Ataxia: a Systematic Review and Meta-analysis

Lacorte E, Bellomo G, Nuovo S, Corbo M, Vanacore N, Piscopo P.

Cerebellum. 2020 Nov 14. doi: 10.1007/s12311-020-01210-x. Online ahead of print.

The use of motor learning and neural plasticity in rehabilitation for ataxic hemiparesis: A case report

Crum EO, Baltz MJ, Krause DA.

Physiother Theory Pract. 2020 Nov;36(11):1256-1265. doi: 10.1080/09593985.2019.1566941. Epub 2019 Jan 27.

Metabolic profiling reveals dysregulated lipid metabolism and potential biomarkers associated with the development and progression of Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)

Zafarullah M, Palczewski G, Rivera SM, Hessl DR, Tassone F.

FASEB J. 2020 Dec;34(12):16676-16692. doi: 10.1096/fj.202001880R. Epub 2020 Nov 1.

Abdominal pain as first manifestation of lyme neuroborreliosis in children, case report and review of literature

Savasta S, Fiorito I, Foiadelli T, Pichiecchio A, Cambieri P, Mariani B, Marone P, Marseglia G.

Ital J Pediatr. 2020 Nov 23;46(1):172. doi: 10.1186/s13052-020-00936-y.

Novel insights toward human stroke-related epigenetics: circular RNA and its impact in poststroke processes

Silva PW, M Shimon SM, de Brito LM, Reis-das-Mercês L, Magalhães L, Araújo G, Ribeiro-Dos-Santos Â, Vidal AF.

Epigenomics. 2020 Nov 26. doi: 10.2217/epi-2020-0128. Online ahead of print.

A serial SPECT-CT study in a celiac disease patient with cerebellar ataxia and psychiatric symptoms

Schmidt JJ, Schmidt GJ, Tolentino JC, Simoes EN, Obongo A, Tolentino Y, Coelho FA, Landesmann MCPP, Fonseca LMB, Lacerda GCB, Schmidt SL.

Neurol Sci. 2020 Nov 23. doi: 10.1007/s10072-020-04908-2. Online ahead of print.

Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative Disorder

Rüsch CT, Wortmann SB, Kovacs-Nagy R, Grehten P, Häberle J, Latal B, Stettner GM.

Neuropediatrics. 2020 Nov 23. doi: 10.1055/s-0040-1715628. Online ahead of print.

Improved Neuroimaging Findings and Cognitive Function in a Case of High-altitude Cerebral Edema

Urushida Y, Kikuchi Y, Shimizu C, Amari M, Kawarabayashi T, Nakamura T, Ikeda Y, Takatama M, Shoji M.

Intern Med. 2020 Nov 23. doi: 10.2169/internalmedicine.5747-20. Online ahead of print.

Finding the Needle in the Hay Stack: Population-based Study of Prediagnostic Symptomatic Interval in Children With CNS Tumors

Goldman RD, Cochrane DD, Dahiya A, Mah H, Buttar A, Lambert C, Cheng S.

J Pediatr Hematol Oncol. 2020 Nov 23. doi: 10.1097/MPH.0000000000002012. Online ahead of print.

Gayet Wernicke's encephalopathy with cortical damage following a subtotal gastrectomy: An uncommon association

Benzalim M, Arharas S, Alj S, Elouardi Y, Khallouki M.

Radiol Case Rep. 2020 Nov 4;16(1):94-97. doi: 10.1016/j.radcr.2020.10.049. eCollection 2021 Jan.

Abnormal Saccadic Oscillations Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Encephalopathy and Ataxia

Wright D, Rowley R, Halks-Wellstead P, Anderson T, Wu TY.

Mov Disord Clin Pract. 2020 Nov 2;7(8):980-982. doi: 10.1002/mdc3.13101. eCollection 2020 Nov.

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient

Zhang C, Deng X, Wen Y, He F, Yin F, Peng J.

BMC Med Genet. 2020 Nov 26;21(1):235. doi: 10.1186/s12881-020-01162-3.