Clinical and radiological features of Posterior Cortical Atrophy (PCA) in a GRN mutation carrier: a case report

Giunta M, Libri I, Premi E, Brattini C, Paghera B, Archetti S, Gasparotti R, Padovani A, Borroni B, Benussi A.

Eur J Neurol. 2020 Oct 8. doi: 10.1111/ene.14574. Online ahead of print.

CIM6P/IGF-2 Receptor Ligands Reverse Deficits in Angelman Syndrome Model Mice

Cruz E, Descalzi G, Steinmetz A, Scharfman HE, Katzman A, Alberini CM.

Autism Res. 2020 Oct 27. doi: 10.1002/aur.2418. Online ahead of print.

Identification of a pre-possible multiple system atrophy phase

Osaki Y, Morita Y, Miyamoto Y, Ohtsuru S, Shogase T, Furushima T, Furuya H.

Acta Neurol Scand. 2020 Oct 28. doi: 10.1111/ane.13367. Online ahead of print.

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood

Döring JH, Saffari A, Bast T, Brockmann K, Ehrhardt L, Fazeli W, Janzarik WG, Kluger G, Muhle H, Møller RS, Platzer K, Santos JL, Bache I, Bertsche A, Bonfert M, Borggräfe I, Broser PJ, Datta AN, Hamm

Biomedicines. 2020 Oct 28;8(11):E456. doi: 10.3390/biomedicines8110456.

How specific are non-motor symptoms in the prodrome of Parkinson's disease compared to other movement disorders?

Moscovich M, Heinzel S, Postuma RB, Reilmann R, Klockgether T, Jacobi H, Höglinger G, Berg D.

Parkinsonism Relat Disord. 2020 Oct 5:S1353-8020(20)30778-1. doi: 10.1016/j.parkreldis.2020.10.003. Online ahead of print.

Accurate detection of cerebellar smooth pursuit eye movement abnormalities via mobile phone video and machine learning

Chang Z, Chen Z, Stephen CD, Schmahmann JD, Wu HT, Sapiro G, Gupta AS.

Sci Rep. 2020 Oct 29;10(1):18641. doi: 10.1038/s41598-020-75661-x.

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

Algahtani H, Shirah B, Almatrafi S, Al-Qahtani MH, Abdulkareem AA, Naseer MI.

Neurol Res. 2020 Oct 4:1-7. doi: 10.1080/01616412.2020.1831331. Online ahead of print.

Neurotherapeutic effect of Hyptis spp. leaf extracts in Caenorhabditis elegans models of tauopathy and polyglutamine disease: Role of the glutathione redox cycle

Vilasboas-Campos D, Costa MD, Teixeira-Castro A, Rios R, Silva FG, Bessa C, Dias ACP, Maciel P.

Free Radic Biol Med. 2020 Oct 20:S0891-5849(20)31292-2. doi: 10.1016/j.freeradbiomed.2020.10.018. Online ahead of print.

Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 Variants

Eckenweiler M, Mayr JA, Grünert S, Abicht A, Korinthenberg R.

Neuropediatrics. 2020 Oct 21. doi: 10.1055/s-0040-1715631. Online ahead of print.

Sialidosis Type I without a Cherry Red Spot- Is There a Genetic Basis?

Neeraja K, Holla VV, Prasad S, Surisetti BK, Rakesh K, Kamble N, Yadav R, Pal PK.

J Mov Disord. 2020 Oct 31. doi: 10.14802/jmd.20083. Online ahead of print.

Early-onset severe spinocerebellar ataxia 42 with neurodevelopmental deficits (SCA42ND): Case report, pharmacological trial, and literature review

Casas-Alba D, López-Sala L, Pérez-Ordóñez M, Mari-Vico R, Bolasell M, Martínez-Monseny AF, Muchart J, Fernández-Fernández JM, Martorell L, Serrano M.

Am J Med Genet A. 2020 Oct 24. doi: 10.1002/ajmg.a.61939. Online ahead of print.

Safety assessment of metarrestin in dogs: A clinical candidate targeting a subnuclear structure unique to metastatic cancer cells

Bourdi M, Rudloff U, Patnaik S, Marugan J, Terse PS.

Regul Toxicol Pharmacol. 2020 Oct;116:104716. doi: 10.1016/j.yrtph.2020.104716. Epub 2020 Jun 30.

Spinocerebellar Ataxia-Like Presentation of the M233V PSEN1 Mutation

Seliverstov Y, Kanivets I, Illarioshkin S.

Cerebellum. 2020 Oct;19(5):744-747. doi: 10.1007/s12311-020-01161-3.

New Nonsense Variant c.2983G>T; p.Glu995* in the CACNA1A Gene Causes Progressive Autosomal Dominant Ataxia

Saathoff Y, Biskup S, Funke C, Roth C.

J Mov Disord. 2020 Oct 31. doi: 10.14802/jmd.20082. Online ahead of print.

Mutant IDH1 Enhances Temozolomide Sensitivity via Regulation of the ATM/CHK2 Pathway in Glioma

Lin L, Cai J, Tan Z, Meng X, Li R, Li Y, Jiang C.

Cancer Res Treat. 2020 Oct 13. doi: 10.4143/crt.2020.506. Online ahead of print.