Inicia sesión Registrate Mi Biblioteca idioma

Idioma

biblioteca idioma abrir menu

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.

Ataxia

6944 ARTíCULOS , VIENDO DEL 6916 AL 6930

PUBMED

A longitudinal investigation into cognition and disease progression in spinocerebellar ataxia types 1, 2, 3, 6, and 7.

Moriarty A, Cook A, Hunt H, Adams ME, Cipolotti L, Giunti P.

Orphanet J Rare Dis. 2016 Jun 22;11(1):82. doi: 10.1186/s13023-016-0447-6.

0

0

0

PUBMED

Impairment in motor reprogramming in Friedreich ataxia reflecting possible cerebellar dysfunction.

Corben LA, Delatycki MB, Bradshaw JL, Horne MK, Fahey MC, Churchyard AJ, Georgiou-Karistianis N.

J Neurol. 2010 May;257(5):782-91. doi: 10.1007/s00415-009-5410-1.

0

0

0

PUBMED

Role of dynamic and mitochondrial mutations in neurodegenerative diseases with ataxia: lower repeats and LNAs at multiple loci as alternative pathogenesis.

Gul Lone W, Poornima S, Meena AK, Rao KP, Hasan Q.

J Mol Neurosci. 2014 Dec;54(4):837-47. doi: 10.1007/s12031-014-0431-3.

0

0

0

PUBMED

Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.

Gan SR, Wang J, Figueroa KP, Pulst SM, Tomishon D, Lee D, Perlman S, Wilmot G, Gomez CM, Schmahmann J, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind MD, Xia G, Subramony SH, Ash

Tremor Other Hyperkinet Mov (N Y). 2017 Oct 9;7:492. doi: 10.7916/D8GM8KRH. eCollection 2017.

0

0

0

PUBMED

Challenges ahead for trials in Friedreich's ataxia.

Lynch DR, Kichula E.

Lancet Neurol. 2016 Dec;15(13):1300-1301. doi: 10.1016/S1474-4422(16)30281-2. No abstract available.

0

0

0

PUBMED

The NRF2 Signaling Network Defines Clinical Biomarkers and Therapeutic Opportunity in Friedreich's Ataxia

La Rosa P, Bertini ES, Piemonte F.

Int J Mol Sci. 2020 Jan 30;21(3):916. doi: 10.3390/ijms21030916.

0

0

0

PUBMED

The reciprocal cerebellar circuitry in human hereditary ataxia.

Koeppen AH, Ramirez RL, Bjork ST, Bauer P, Feustel PJ.

Cerebellum. 2013 Aug;12(4):493-503. doi: 10.1007/s12311-013-0456-0.

0

0

0

PUBMED

A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia.

Al Tassan N, Khalil D, Shinwari J, Al Sharif L, Bavi P, Abduljaleel Z, Abu Dhaim N, Magrashi A, Bobis S, Ahmed H, Alahmed S, Bohlega S.

Hum Mutat. 2012 Feb;33(2):351-4. doi: 10.1002/humu.21650.

0

0

0

PUBMED

Generation of induced pluripotent stem cells from a patient with spinocerebellar ataxia type 3.

Soong BW, Syu SH, Wen CH, Ko HW, Wu ML, Hsieh PC, Hwang SM, Lu HE.

Stem Cell Res. 2017 Jan;18:29-32. doi: 10.1016/j.scr.2016.12.017. Epub 2016 Dec 9.

0

0

0

PUBMED

Cerebellar ataxia by enhanced Ca(V)2.1 currents is alleviated by Ca2+-dependent K+-channel activators in Cacna1a(S218L) mutant mice.

Gao Z, Todorov B, Barrett CF, van Dorp S, Ferrari MD, van den Maagdenberg AM, De Zeeuw CI, Hoebeek FE.

J Neurosci. 2012 Oct 31;32(44):15533-46. doi: 10.1523/JNEUROSCI.2454-12.2012.

0

0

0

PUBMED

Acetyl-DL-leucine improves gait variability in patients with cerebellar ataxia-a case series.

Schniepp R, Strupp M, Wuehr M, Jahn K, Dieterich M, Brandt T, Feil K.

Cerebellum Ataxias. 2016 Apr 12;3:8. doi: 10.1186/s40673-016-0046-2.

0

0

0

PUBMED

Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study.

Renaud M, Anheim M, Kamsteeg EJ, Mallaret M, Mochel F, Vermeer S, Drouot N, Pouget J, Redin C, Salort-Campana E, Kremer HP, Verschuuren-Bemelmans CC, Muller J, Scheffer H, Durr A, Tranchant C, Koenig

JAMA Neurol. 2014 Oct;71(10):1305-10. doi: 10.1001/jamaneurol.2014.193.

0

0

0

PUBMED

Autonomic function testing in spinocerebellar ataxia type 2.

Indelicato E, Fanciulli A, Ndayisaba JP, Nachbauer W, Granata R, Wanschitz J, Wagner M, Gizewski ER, Poewe W, Wenning GK, Boesch S.

Clin Auton Res. 2018 Feb 12. doi: 10.1007/s10286-018-0504-4. [Epub ahead of print]

0

0

0

PUBMED

Premature ageing of the immune system underlies immunodeficiency in ataxia telangiectasia.

Exley AR, Buckenham S, Hodges E, Hallam R, Byrd P, Last J, Trinder C, Harris S, Screaton N, Williams AP, Taylor AM, Shneerson JM.

Clin Immunol. 2011 Jul;140(1):26-36. doi: 10.1016/j.clim.2011.03.007.

0

0

0

PUBMED

A case of a 17-year-old male with neurofascin-155 antibody-positive chronic inflammatory demyelinating polyradiculoneuropathy presenting with tremor and ataxia.

Itaya K, Inoue M, Iizuka N, Shimizu Y, Yuki N, Ichikawa H.

Rinsho Shinkeigaku. 2016 Sep 29;56(9):633-6. doi: 10.5692/clinicalneurol.cn-000853.

0

0

0

Comentarios

En ningún caso la información facilitada constituye asesoramiento por parte de Zambon

Con el aval de:

Logo SEN Logo HONcode Logo WIS

En colaboración con:

Zambon Neuroacademy