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Bibliografía Científica

Artículos por temáticas

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

Corea y enfermedad de Huntington

262 ARTíCULOS , VIENDO DEL 76 AL 90

PUBMED

Paliperidone Long-Acting Injections in Huntington's Disease for Motor and Behavioural Disturbances.

van Oosterom N, Theodoros T.

Clin Drug Investig. 2019 Apr;39(4):407-410. doi: 10.1007/s40261-019-00759-8.

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PUBMED

Antisense oligonucleotides might change the therapeutic landscape for Huntington's disease.

Paulsen JS, Coffey CS.

Lancet Neurol. 2019 Oct;18(10):911-912. doi: 10.1016/S1474-4422(19)30329-1. No abstract available.

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PUBMED

Bim contributes to the progression of Huntington's disease-associated phenotypes.

Roberts SL, Evans T, Yang Y, Fu Y, Button RW, Sipthorpe RJ, Cowan K, Valionyte E, Anichtchik O, Li H, Lu B, Luo S.

Hum Mol Genet. 2020 Jan 15;29(2):216-227. doi: 10.1093/hmg/ddz275.

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PUBMED

Positive allosteric modulation of the type 1 cannabinoid receptor reduces the signs and symptoms of Huntington's disease in the R6/2 mouse model.

Laprairie RB, Bagher AM, Rourke JL, Zrein A, Cairns EA, Kelly MEM, Sinal CJ, Kulkarni PM, Thakur GA, Denovan-Wright EM.

Neuropharmacology. 2019 Mar 30;151:1-12. doi: 10.1016/j.neuropharm.2019.03.033. [Epub ahead of print]

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PUBMED

Clinical and Genetic Profiles in Chinese Patients with Huntington's Disease: A Ten-year Multicenter Study in China.

Li HL, Li XY, Dong Y, Zhang YB, Cheng HR, Gan SR, Liu ZJ, Ni W, Burgunder JM, Yang XW, Wu ZY.

Aging Dis. 2019 Oct 1;10(5):1003-1011. doi: 10.14336/AD.2018.0911. eCollection 2019 Oct.

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PUBMED

Chorea-related mutations in PDE10A result in aberrant compartmentalization and functionality of the enzyme.

Tejeda GS, Whiteley EL, Deeb TZ, Bürli RW, Moss SJ, Sheridan E, Brandon NJ, Baillie GS.

Proc Natl Acad Sci U S A. 2020 Jan 7;117(1):677-688. doi: 10.1073/pnas.1916398117. Epub 2019 Dec 23.

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PUBMED

Striatal Cholesterol Precursors Are Altered with Age in Female Huntington's Disease Model Mice.

Pfalzer AC, Wages PA, Porter NA, Bowman AB.

J Huntingtons Dis. 2019 Apr 3. doi: 10.3233/JHD-180321. [Epub ahead of print]

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PUBMED

A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.

Ciosi M, Maxwell A, Cumming SA, Hensman Moss DJ, Alshammari AM, Flower MD, Durr A, Leavitt BR, Roos RAC; TRACK-HD team.; Enroll-HD team., Holmans P, Jones L, Langbehn DR, Kwak S, Tabrizi SJ, Monckton

EBioMedicine. 2019 Oct 4. pii: S2352-3964(19)30624-3. doi: 10.1016/j.ebiom.2019.09.020. [Epub ahead of print]

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PUBMED

Conformational studies of pathogenic expanded polyglutamine protein deposits from Huntington's disease.

Matlahov I, van der Wel PC.

Exp Biol Med (Maywood). 2019 Dec;244(17):1584-1595. doi: 10.1177/1535370219856620. Epub 2019 Jun 15. No abstract available.

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PUBMED

Striatal morphology and neurocognitive dysfunction in Huntington disease: The IMAGE-HD study.

Wilkes FA, Abaryan Z, Ching CRK, Gutman BA, Madsen SK, Walterfang M, Velakoulis D, Stout JC, Chua P, Egan GF, Thompson PM, Looi JCL, Georgiou-Karistianis N.

Psychiatry Res Neuroimaging. 2019 Sep 30;291:1-8. doi: 10.1016/j.pscychresns.2019.07.003. Epub 2019 Jul 12.

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PUBMED

Treatment with JQ1, a BET bromodomain inhibitor, is selectively detrimental to R6/2 Huntington's disease mice.

Kedaigle AJ, Reidling JC, Lim RG, Adam M, Wu J, Wassie B, Stocksdale JT, Casale MS, Fraenkel E, Thompson LM.

Hum Mol Genet. 2019 Nov 7. pii: ddz264. doi: 10.1093/hmg/ddz264. [Epub ahead of print]

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PUBMED

Association of CAG Repeats With Long-term Progression in Huntington Disease.

Langbehn DR, Stout JC, Gregory S, Mills JA, Durr A, Leavitt BR, Roos RAC, Long JD, Owen G, Johnson HJ, Borowsky B, Craufurd D, Reilmann R, Landwehrmeyer GB, Scahill RI, Tabrizi SJ; TRACK-HD and Track-

JAMA Neurol. 2019 Aug 12. doi: 10.1001/jamaneurol.2019.2368. [Epub ahead of print]

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PUBMED

Longitudinal atrophy characterization of cortical and subcortical gray matter in Huntington's disease patients.

Ramirez-Garcia G, Galvez V, Diaz R, Bayliss L, Fernandez-Ruiz J, Campos-Romo A.

Eur J Neurosci. 2019 Nov 9. doi: 10.1111/ejn.14617. [Epub ahead of print]

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PUBMED

A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?

Milone R, Masson R, Di Cosmo C, Tonacchera M, Bertini V, Guzzetta A, Battini R.

Child Neurol Open. 2019 Feb 12;6:2329048X19828881. doi: 10.1177/2329048X19828881. eCollection 2019.

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PUBMED

18F-FDG PET/CT: an unexpected case of Huntington's disease.

Michels S, Buchholz HG, Rosar F, Heinrich I, Hoffmann MA, Schweiger S, Tüscher O, Schreckenberger M.

BMC Neurol. 2019 May 1;19(1):78. doi: 10.1186/s12883-019-1311-9.

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