Artículos por temáticas

En este apartado encontrará una actualización mensual de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por la International Parkinson & Movement Disorder Society.

Tema

Trastornos del movimiento Enfermedad de Parkinson Distonía Corea y enfermedad de Huntington Ataxia Temblor y temblor esencial Mioclonía y espasmos Tics y síndrome de Tourette Síndrome de piernas inquietas Síndrome de la persona rígida Alteraciones de la marcha Espasticidad COVID-19 y Enfermedades Neurológicas

Año

2025 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 1993

Ataxia

9267 ARTíCULOS , VIENDO DEL 9256 AL 9267

PUBMED

Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family.

Palvadeau R, Kaya-Güleç ZE, Şimşir G, Vural A, Öztop-Çakmak Ö, Genç G, Aygün MS, Falay O, Başak AN, Ertan S.

Neurogenetics. 2020 Jan;21(1):51-58. doi: 10.1007/s10048-019-00595-0. Epub 2019 Nov 19.

PUBMED

Distinguishing ataxia from developmental coordination disorder.

Baxter P.

Dev Med Child Neurol. 2020 Jan;62(1):11. doi: 10.1111/dmcn.14376. Epub 2019 Oct 17. No abstract available.

PUBMED

Guissart C, Harrison AN, Benkirane M, Oncel I, Arslan EA, Chassevent AK, Baraῆano K, Larrieu L, Iascone M, Tenconi R, Claustres M, Eroglu-Ertugrul N, Calvas P, Topaloglu H, Molday RS, Koenig M.

J Neurol. 2020 Jan;267(1):203-213. doi: 10.1007/s00415-019-09579-4. Epub 2019 Oct 14.

PUBMED

Primary Cultures of Pure Embryonic Dorsal Root Ganglia Sensory Neurons as a New Cellular Model for Friedreich's Ataxia

Griso O, Puccio H.

Methods Mol Biol. 2020;2056:241-253. doi: 10.1007/978-1-4939-9784-8_15.

PUBMED

The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins.

Sawada J, Katayama T, Tokashiki T, Kikuchi S, Kano K, Takahashi K, Saito T, Adachi Y, Okamoto Y, Yoshimura A, Takashima H, Hasebe N.

Intern Med. 2020 Jan 15;59(2):277-283. doi: 10.2169/internalmedicine.2905-19. Epub 2019 Sep 26.

PUBMED

Is fatigue an important finding in patients with spinocerebellar ataxia type 10 (SCA10)?

Moro A, Munhoz RP, Camargo CH, Moscovich M, Farah M, Teive HAG.

J Clin Neurosci. 2020 Jan;71:150-152. doi: 10.1016/j.jocn.2019.08.097. Epub 2019 Sep 17.

PUBMED

Paediatric motor phenotypes in early-onset ataxia, developmental coordination disorder, and central hypotonia.

Lawerman TF, Brandsma R, Maurits NM, Martinez-Manzanera O, Verschuuren-Bemelmans CC, Lunsing RJ, Brouwer OF, Kremer HP, Sival DA.

Dev Med Child Neurol. 2020 Jan;62(1):75-82. doi: 10.1111/dmcn.14355. Epub 2019 Sep 17.

PUBMED

Advance Care Plan and Factors Related to Disease Progression in Patients With Spinocerebellar Ataxia Type 1: A Cross-Sectional Study in Thailand.

Gomutbutra P, Brandeland M.

Am J Hosp Palliat Care. 2020 Jan;37(1):46-51. doi: 10.1177/1049909119850797. Epub 2019 May 14.

PUBMED

ATM mutation spectrum in Russian children with ataxia-telangiectasia.

Suspitsin E, Sokolenko A, Bizin I, Tumakova A, Guseva M, Sokolova N, Vakhlyarskaya S, Kondratenko I, Imyanitov E.

Eur J Med Genet. 2020 Jan;63(1):103630. doi: 10.1016/j.ejmg.2019.02.003. Epub 2019 Feb 14.

PUBMED

Whole-exome sequencing identifies rare compound heterozygous mutations in the MSTO1 gene associated with cerebellar ataxia and myopathy.

Li K, Jin R, Wu X.

Eur J Med Genet. 2020 Jan;63(1):103623. doi: 10.1016/j.ejmg.2019.01.013. Epub 2019 Jan 24.

PUBMED

Ataxia Telangiectasia (Louis-Bar Syndrome).

Riboldi GM, Samanta D, Frucht S.

2019 Dec 31. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.

PUBMED

Body composition in Spinocerebellar ataxia type 3 and 10 patients: Comparative study with control group

Leite CMBA, Schieferdecker MEM, Frehner C, Munhoz RP, Ashizawa T, Teive HAG.

Nutr Neurosci. 2020 Jan;23(1):49-54. doi: 10.1080/1028415X.2018.1469282. Epub 2018 May 7.

Artículos por temáticas

Ataxia

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