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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

347 ARTíCULOS , VIENDO DEL 331 AL 345

PUBMED

Inhibition of Drp1 hyperactivation reduces neuropathology and behavioral deficits in zQ175 knock-in mouse model of Huntington's disease.

Zhao Y, Sun X, Qi X.

Biochem Biophys Res Commun. 2018 Dec 9;507(1-4):319-323. doi: 10.1016/j.bbrc.2018.11.031. Epub 2018 Nov 16.

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PUBMED

Perinatal insults and neurodevelopmental disorders may impact Huntington's disease age of diagnosis.

Barkhuizen M, Rodrigues FB, Anderson DG, Winkens B; REGISTRY Investigators of the European Huntington's Disease Network., Wild EJ, Kramer BW, Gavilanes AWD.

Parkinsonism Relat Disord. 2018 May 18. pii: S1353-8020(18)30246-3. doi: 10.1016/j.parkreldis.2018.05.016. [Epub ahead of print]

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PUBMED

Effects of Stimulus-Related Variables on Mental States Recognition in Huntington'S Disease.

Belardinelli MO, Huenefeldt T, Maffi S, Squitieri F, Migliore S.

Int J Neurosci. 2018 Nov 27:1-21. doi: 10.1080/00207454.2018.1552691. [Epub ahead of print]

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Huntington's Disease Outpatient Clinic for Functional Diagnosis and Treatment: Coming to Consensus: How Long Term Care Facility Procedures Complement Specialist Diagnosis and Treatment.

Veenhuizen R, Nijsten H, van Roosmalen P, Lammertsen K, Stor T, de Jager L, de Man J, van der Doelen R, Landa K, Grond V, Heffels J, Groenewoud R, Rovers L, Bakker C, Leiwakabessy S, van der Wedden D,

J Huntingtons Dis. 2018 May 19. doi: 10.3233/JHD-180298. [Epub ahead of print]

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PUBMED

The role of the striatum in linguistic selection: Evidence from Huntington's disease and computational modeling.

Giavazzi M, Daland R, Palminteri S, Peperkamp S, Brugières P, Jacquemot C, Schramm C, Cleret de Langavant L, Bachoud-Lévi AC.

Cortex. 2018 Dec;109:189-204. doi: 10.1016/j.cortex.2018.08.031. Epub 2018 Sep 15.

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PUBMED

Quantification of the Light Subunit of Neurofilament Protein in Cerebrospinal Fluid of Huntington's Disease Patients.

Szejko N, Picón C, García-Caldentey J, de Yebenes JG, Alvarez-Cermeño JC, Villar LM, López-Sendón Moreno JL.

PLoS Curr. 2018 Aug 31;10. pii: ecurrents.hd.280c8f9f7d9fa4f7f0c883d9f8e807da. doi: 10.1371/currents.hd.280c8f9f7d9fa4f7f0c883d9f8e807da.

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PUBMED

Corticostriatal network dysfunction in huntington's disease: Deficits in neural processing, glutamate transport, and ascorbate release.

Rebec GV.

CNS Neurosci Ther. 2018 Feb 21. doi: 10.1111/cns.12828. [Epub ahead of print] Review.

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PUBMED

Morvan Syndrome (Morvan Fibrillary Chorea, MFC).

Masood W, Sitammagari KK.

2020 Jan 15. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.

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PUBMED

Human Umbilical Cord Matrix Stem Cells Reverse Oxidative Stress-Induced Cell Death and Ameliorate Motor Function and Striatal Atrophy in Rat Model of Huntington Disease.

Ebrahimi MJ, Aliaghaei A, Boroujeni ME, Khodagholi F, Meftahi G, Abdollahifar MA, Ahmadi H, Danyali S, Daftari M, Sadeghi Y.

Neurotox Res. 2018 Aug;34(2):273-284. doi: 10.1007/s12640-018-9884-4. Epub 2018 Mar 8.

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PUBMED

Small molecule modulator of protein disulfide isomerase attenuates mutant huntingtin toxicity and inhibits endoplasmic reticulum stress in a mouse model of Huntington's disease.

Zhou X, Li G, Kaplan A, Gaschler MM, Zhang X, Hou Z, Mali J, Zott R, Cremers S, Stockwell BR, Duan W.

Hum Mol Genet. 2018 Feb 16. doi: 10.1093/hmg/ddy061. [Epub ahead of print]

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PUBMED

Epidemiology of Huntington disease in Cyprus: A 20-year retrospective study.

Demetriou CA, Heraclides A, Salafori C, Tanteles GA, Christodoulou K, Christou Y, Zamba-Papanicolaou E.

Clin Genet. 2018 Mar;93(3):656-664. doi: 10.1111/cge.13168. Epub 2018 Feb 8.

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PUBMED

HACE1 is essential for astrocyte mitochondrial function and influences Huntington disease phenotypes in vivo.

Ehrnhoefer DE, Southwell AL, Sivasubramanian M, Qiu X, Villanueva EB, Xie Y, Waltl S, Anderson L, Fazeli A, Casal L, Felczak B, Tsang M, Hayden MR.

Hum Mol Genet. 2018 Jan 15;27(2):239-253. doi: 10.1093/hmg/ddx394.

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PUBMED

FAN1 modifies Huntington's disease progression by stabilising the expanded HTT CAG repeat.

Goold R, Flower M, Moss DH, Medway C, Wood-Kaczmar A, Andre R, Farshim P, Bates GP, Holmans P, Jones L, Tabrizi SJ.

Hum Mol Genet. 2018 Oct 24. doi: 10.1093/hmg/ddy375. [Epub ahead of print]

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PUBMED

Identification of differentially expressed genes and regulatory relationships in Huntington's disease by bioinformatics analysis.

Dong X, Cong S.

Mol Med Rep. 2018 Mar;17(3):4317-4326. doi: 10.3892/mmr.2018.8410. Epub 2018 Jan 9.

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PUBMED

The ubiquitin ligase UBR5 suppresses proteostasis collapse in pluripotent stem cells from Huntington's disease patients.

Koyuncu S, Saez I, Lee HJ, Gutierrez-Garcia R, Pokrzywa W, Fatima A, Hoppe T, Vilchez D.

Nat Commun. 2018 Jul 23;9(1):2886. doi: 10.1038/s41467-018-05320-3.

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