Artículos por temáticas

Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome.

Ma L, Herren AW, Espinal G, Randol J, McLaughlin B, Martinez-Cerdeño V, Pessah IN, Hagerman RJ, Hagerman PJ.

Acta Neuropathol Commun. 2019 Sep 3;7(1):143. doi: 10.1186/s40478-019-0796-1.

Osteochondral fragmentation of the cervical articular process joints within a population of horses with signs of ataxia and/or cervical pain.

[No authors listed]

Equine Vet J. 2019 Sep;51 Suppl 53:29. doi: 10.1111/evj.49_13152. No abstract available.

Neurosyphilis presenting as pure cerebellar ataxia: an atypical manifestation.

Garg D, Vibha D, Pandit AK, Srivastava AK.

BMJ Case Rep. 2019 Aug 31;12(8). pii: e231058. doi: 10.1136/bcr-2019-231058.

Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China.

Zhou Y, Yuan Y, Liu Z, Zeng S, Chen Z, Shen L, Jiang H, Xia K, Tang B, Wang J.

J Neurol. 2019 Aug 30. doi: 10.1007/s00415-019-09519-2. [Epub ahead of print]

Childhood-onset cerebellar ataxia in Japan: A questionnaire-based survey.

Ono H, Shimizu-Motohashi Y, Maruo K, Takeshita E, Ishiyama A, Saito T, Komaki H, Nakagawa E, Sasaki M.

Brain Behav. 2019 Aug 30:e01392. doi: 10.1002/brb3.1392. [Epub ahead of print]

Functional parameter measurements in children with ataxia telangiectasia

Shenhod E, Benzeev B, Sarouk I, Heimer G, Nissenkorn A.

Dev Med Child Neurol. 2020 Feb;62(2):207-213. doi: 10.1111/dmcn.14334. Epub 2019 Aug 30.

Very-late-onset Friedreich's ataxia: diagnosis in a kindred with late-onset cerebellar ataxia

Fearon C, Lonergan R, Ferguson D, Byrne S, Bradley D, Langan Y, Redmond J.

Pract Neurol. 2020 Feb;20(1):55-58. doi: 10.1136/practneurol-2019-002368. Epub 2019 Aug 29.

Quantitative susceptibility mapping in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)

Xie F, Weihua L, Lirong O, Wang X, Xing W.

Acta Radiol. 2020 Apr;61(4):520-527. doi: 10.1177/0284185119868906. Epub 2019 Aug 26.

Oral mobility reflects rate of progression in advanced Friedreich's ataxia.

Borel S, Gatignol P, Smail M, Monin ML, Ewenczyk C, Bouccara D, Durr A.

Ann Clin Transl Neurol. 2019 Aug 25. doi: 10.1002/acn3.50879. [Epub ahead of print]

Excision of the expanded GAA repeats corrects cardiomyopathy phenotypes of iPSC-derived Friedreich's ataxia cardiomyocytes.

Li J, Rozwadowska N, Clark A, Fil D, Napierala JS, Napierala M.

Stem Cell Res. 2019 Aug 7;40:101529. doi: 10.1016/j.scr.2019.101529. [Epub ahead of print]

Extensive cerebellar and thalamic degeneration in spinocerebellar ataxia type 10.

Hernandez-Castillo CR, Diaz R, Vaca-Palomares I, Torres DL, Chirino A, Campos-Romo A, Ochoa A, Rasmussen A, Fernandez-Ruiz J.

Parkinsonism Relat Disord. 2019 Aug 19. pii: S1353-8020(19)30367-0. doi: 10.1016/j.parkreldis.2019.08.011. [Epub ahead of print]

Withaferin A inhibits expression of ataxia telangiectasia and Rad3-related kinase and enhances sensitivity of human breast cancer cells to cisplatin.

Hahm ER, Lee J, Abella T, Singh SV.

Mol Carcinog. 2019 Aug 22. doi: 10.1002/mc.23104. [Epub ahead of print]

Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2.

Egorova PA, Bezprozvanny IB.

Neurotherapeutics. 2019 Aug 21. doi: 10.1007/s13311-019-00777-6. [Epub ahead of print] Review.

Ataxia-telangiectasia mutated coordinates the ovarian DNA repair and atresia-initiating response to phosphoramide mustard

Clark KL, Keating AF.

Biol Reprod. 2020 Feb 12;102(1):248-260. doi: 10.1093/biolre/ioz160.

Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.

Niewiadomska-Cimicka A, Trottier Y.

Neurotherapeutics. 2019 Aug 20. doi: 10.1007/s13311-019-00778-5. [Epub ahead of print] Review.