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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

263 ARTíCULOS , VIENDO DEL 91 AL 105

PUBMED

Myelin Breakdown in Human Huntington's Disease: Multi-Modal Evidence from Diffusion MRI and Quantitative Magnetization Transfer.

Bourbon-Teles J, Bells S, Jones DK, Coulthard E, Rosser A, Metzler-Baddeley C.

Neuroscience. 2019 Apr 1;403:79-92. doi: 10.1016/j.neuroscience.2017.05.042. Epub 2017 Jun 1.

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PUBMED

Discovery of a potent small molecule inhibiting Huntington's disease (HD) pathogenesis via targeting CAG repeats RNA and Poly Q protein.

Khan E, Mishra SK, Mishra R, Mishra A, Kumar A.

Sci Rep. 2019 Nov 14;9(1):16872. doi: 10.1038/s41598-019-53410-z.

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PUBMED

You can dance if you want to: A case of Sydenham's chorea.

Lubberdink AL, Sharif S, Pardhan K.

Am J Emerg Med. 2019 Aug 24:158414. doi: 10.1016/j.ajem.2019.158414. [Epub ahead of print]

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PUBMED

The Onset and Progression of Hippocampal Synaptic Plasticity Deficits in the Q175FDN Mouse Model of Huntington Disease.

Quirion JG, Parsons MP.

Front Cell Neurosci. 2019 Jul 17;13:326. doi: 10.3389/fncel.2019.00326. eCollection 2019.

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PUBMED

Chorea-like symptoms and high blood concentration of ceftriaxone in a patient undergoing hemodialysis: A case report.

Yokoyama Y, Hosokawa N, Kudo T, Goda H, Ito K, Suzuki M, Funakoshi R.

J Infect Chemother. 2019 Oct 31. pii: S1341-321X(19)30305-8. doi: 10.1016/j.jiac.2019.10.005. [Epub ahead of print]

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PUBMED

Striatal Interneurons in Transgenic Nonhuman Primate Model of Huntington's Disease.

Lallani SB, Villalba RM, Chen Y, Smith Y, Chan AWS.

Sci Rep. 2019 Mar 5;9(1):3528. doi: 10.1038/s41598-019-40165-w.

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PUBMED

Cerebellar degeneration correlates with motor symptoms in Huntington disease.

Singh-Bains MK, Mehrabi NF, Sehji T, Austria MDR, Tan AYS, Tippett LJ, Dragunow M, Waldvogel HJ, Faull RLM.

Ann Neurol. 2019 Mar;85(3):396-405. doi: 10.1002/ana.25413. Epub 2019 Feb 4.

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PUBMED

Leptin deficiency reverses high metabolic state and weight loss without affecting central pathology in the R6/2 mouse model of Huntington's disease.

Sjögren M, Soylu-Kucharz R, Dandunna U, Stan TL, Cavalera M, Sandelius Å, Zetterberg H, Björkqvist M.

Neurobiol Dis. 2019 Dec;132:104560. doi: 10.1016/j.nbd.2019.104560. Epub 2019 Aug 13.

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PUBMED

IKKβ slows Huntington's disease progression in R6/1 mice.

Ochaba J, Fote G, Kachemov M, Thein S, Yeung SY, Lau AL, Hernandez S, Lim RG, Casale M, Neel MJ, Monuki ES, Reidling J, Housman DE, Thompson LM, Steffan JS.

Proc Natl Acad Sci U S A. 2019 May 28;116(22):10952-10961. doi: 10.1073/pnas.1814246116. Epub 2019 May 14.

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PUBMED

Sample enrichment for clinical trials to show delay of onset in huntington disease.

Paulsen JS, Lourens S, Kieburtz K, Zhang Y.

Mov Disord. 2019 Jan 14. doi: 10.1002/mds.27595. [Epub ahead of print]

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PUBMED

Body composition and bone mineral density in Huntington's disease.

Costa de Miranda R, Di Lorenzo N, Andreoli A, Romano L, De Santis GL, Gualtieri P, De Lorenzo A.

Nutrition. 2019 Mar;59:145-149. doi: 10.1016/j.nut.2018.08.005. Epub 2018 Aug 21.

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PUBMED

Amelioration of Huntington's disease phenotype in astrocytes derived from iPSC-derived neural progenitor cells of Huntington's disease monkeys.

Cho IK, Yang B, Forest C, Qian L, Chan AWS.

PLoS One. 2019 Mar 21;14(3):e0214156. doi: 10.1371/journal.pone.0214156. eCollection 2019.

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PUBMED

Validity of irritability in Huntington's disease: A scoping review.

Simpson J, Dale M, Theed R, Gunn S, Zarotti N, Eccles FJR.

Cortex. 2019 Nov;120:353-374. doi: 10.1016/j.cortex.2019.06.012. Epub 2019 Jul 8. Review.

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PUBMED

PGC-1α, Sirtuins and PARPs in Huntington's Disease and Other Neurodegenerative Conditions: NAD+ to Rule Them All.

Lloret A, Beal MF.

Neurochem Res. 2019 May 7. doi: 10.1007/s11064-019-02809-1. [Epub ahead of print]

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PUBMED

Reverse pre-symptomatic testing for Huntington disease: double disclosure when 25% at-risk children reveal the genetic status to their parent.

Bonnard A, Herson A, Gargiulo M, Durr A.

Eur J Hum Genet. 2019 Jan;27(1):22-27. doi: 10.1038/s41431-018-0255-7. Epub 2018 Sep 11.

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