Artículos por temáticas
En este apartado encontrará una actualización mensual de artículos sobre la enfermedad de Alzheimer/demencias y sobre los Trastornos del Movimiento clasificados según los 11 tipos establecidos por la International Parkinson & Movement Disorder Society.
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173896 ARTíCULOS , VIENDO DEL 172081 AL 172095
Termsarasab P.
Continuum (Minneap Minn). 2019 Aug;25(4):1001-1035. doi: 10.1212/CON.0000000000000763.
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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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van der Graaf LM, Gardiner SL, Tok M, Brands T, Boogaard MW, Pepers BA, Eussen B, de Klein A, Aziz NA, Freund C, Buijsen RAM, van Roon-Mom WMC.
Stem Cell Res. 2019 Aug;39:101498. doi: 10.1016/j.scr.2019.101498. Epub 2019 Jul 12.
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Neuroacanthocytosis: a case report of chorea-acanthocytosis.
Xiang Y, Li S, Liu X, Li J, Sun Q, Chen Y, Du Y, Wu J.
J Integr Neurosci. 2019 Jun 30;18(2):197-201. doi: 10.31083/j.jin.2019.02.165.
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Different clinical profiles in Huntington disease show distinct patterns of brain alterations.
Kelsey R.
Nat Rev Neurol. 2019 Sep;15(9):492. doi: 10.1038/s41582-019-0237-6. No abstract available.
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Adult-onset Huntington disease: An update.
[No authors listed]
Nursing. 2019 Jul;49(7):43-44. doi: 10.1097/01.NURSE.0000569736.14018.ce. No abstract available.
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Adult-onset Huntington disease: An update.
Urrutia NL.
Nursing. 2019 Jul;49(7):36-43. doi: 10.1097/01.NURSE.0000559914.46449.29.
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Iodice A, Carecchio M, Zorzi G, Garavaglia B, Spagnoli C, Salerno GG, Frattini D, Mencacci NE, Invernizzi F, Veneziano L, Mantuano E, Angriman M, Fusco C.
Brain Dev. 2019 Aug;41(7):643. doi: 10.1016/j.braindev.2019.04.011. Epub 2019 Apr 30. No abstract available.
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Kendrick LM, Hudgell D, Hellman A, Weaver MS.
J Palliat Care. 2019 Jul;34(3):205-207. doi: 10.1177/0825859719835560. Epub 2019 Apr 5.
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Efficacy of ethyl-EPA as a treatment for Huntington disease: a systematic review and meta-analysis.
Morsy S, Khalil SM, Doheim MF, Kamel MG, El-Basiony DSM, Ahmed Hassan HI, Eisa AA, Anh Ngoc CT, Dang NP, Hirayama K, Huy NT.
Acta Neuropsychiatr. 2019 Aug;31(4):175-185. doi: 10.1017/neu.2019.11. Epub 2019 Mar 20.
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27 years of prenatal diagnosis for Huntington disease in the United Kingdom.
Piña-Aguilar RE, Simpson SA, Alshatti A, Clarke A, Craufurd D, Dorkins H, Doye K, Lahiri N, Lashwood A, Lynch C, Miller C, Morton S, O'Driscoll M, Quarrell OW, Rae D, Strong M, Tomlinson C, Turnpenny
Genet Med. 2019 Jul;21(7):1639-1643. doi: 10.1038/s41436-018-0367-z. Epub 2018 Dec 14.
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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.
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Acute cerebellar ataxia: a rare Toscana Virus (TOSV) meningoencephalitis complication
Suardi LR, Di Lauria N, Pozzi M, Rogasi PG, Barilaro A, Azzolini F, Prestipino E, Colao MG, Rossolini GM, Bartoloni A.
Int J Neurosci. 2020 Mar;130(3):276-278. doi: 10.1080/00207454.2019.1673748. Epub 2019 Oct 7.
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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.
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Chen Y, Chen G, Li J, Huang YY, Li Y, Lin J, Chen LZ, Lu JP, Wang YQ, Wang CX, Pan LK, Xia XF, Yi X, Chen CB, Zheng XW, Guo ZQ, Pan JJ.
JAMA Netw Open. 2019 Sep 4;2(9):e1911895. doi: 10.1001/jamanetworkopen.2019.11895.
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