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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.

Ataxia

408 ARTíCULOS , VIENDO DEL 136 AL 150

PUBMED

The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.

Saigoh K, Mitsui J, Hirano M, Shioyama M, Samukawa M, Ichikawa Y, Goto J, Tsuji S, Kusunoki S.

Parkinsonism Relat Disord. 2015 Mar;21(3):332-4. doi: 10.1016/j.parkreldis.2014.12.028. No abstract available.

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New insights into the pathogenesis and therapeutics of episodic ataxia type 1.

D'Adamo MC, Hasan S, Guglielmi L, Servettini I, Cenciarini M, Catacuzzeno L, Franciolini F.

Front Cell Neurosci. 2015 Aug 19;9:317. doi: 10.3389/fncel.2015.00317. Review.

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PUBMED

Progressive Ataxia and Palatal Tremor.

Zuzuárregui JR, Frank SA.

JAMA Neurol. 2015 Oct;72(10):1195. doi: 10.1001/jamaneurol.2015.1114. No abstract available.

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PUBMED

Ataxia-telangiectasia - A historical review and a proposal for a new designation: ATM syndrome.

Teive HA, Moro A, Moscovich M, Arruda WO, Munhoz RP, Raskin S, Ashizawa T.

J Neurol Sci. 2015 Aug 15;355(1-2):3-6. doi: 10.1016/j.jns.2015.05.022. Review.

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Ocular flutter and ataxia without cognitive impairment associated with steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT).

Lee HJ, Jeon K, Lee JY, Lee JE, Bae DW, Oh YS, Cho AH, Kim W.

J Neurol Sci. 2015 Dec 15;359(1-2):86-7. doi: 10.1016/j.jns.2015.10.037. No abstract available.

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PUBMED

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1.

Bettencourt C, de Yébenes JG, López-Sendón JL, Shomroni O, Zhang X, Qian SB, Bakker IM, Heetveld S, Ros R, Quintáns B, Sobrido MJ, Bevova MR, Jain S, Bugiani M, Heutink P, Rizzu P.

Cerebellum. 2015 Jun;14(3):378-81. doi: 10.1007/s12311-014-0643-7. No abstract available.

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PUBMED

Teaching NeuroImages: Corpus callosum splenium hyperintensity in fragile X-associated tremor ataxia syndrome.

Renard D, Fourcade G, Castelnovo G.

Neurology. 2015 Jun 2;84(22):e194. doi: 10.1212/WNL.0000000000001652. No abstract available.

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PUBMED

Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutations.

Mancini C, Nassani S, Guo Y, Chen Y, Giorgio E, Brussino A, Di Gregorio E, Cavalieri S, Lo Buono N, Funaro A, Pizio NR, Nmezi B, Kyttala A, Santorelli FM, Padiath QS, Hakonarson H, Zhang H, Brusco A.

J Neurol. 2015 Jan;262(1):173-8. doi: 10.1007/s00415-014-7553-y.

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PUBMED

Mutation analysis of 6 spinocerebellar ataxia (SCA) types in patients from southern Turkey.

Pazarci P, Kasap H, Koç AF, Altunbaşak S, Erkoç MA.

Turk J Med Sci. 2015;45(6):1228-33.

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PUBMED

Antibodies to dendritic neuronal surface antigens in opsoclonus myoclonus ataxia syndrome.

Panzer JA, Anand R, Dalmau J, Lynch DR.

J Neuroimmunol. 2015 Sep 15;286:86-92. doi: 10.1016/j.jneuroim.2015.07.007.

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PUBMED

Opsoclonus-ataxia syndrome associated with ovarian mature teratoma.

Kanno K, Kin S, Hirose M, Suzuki S, Watanabe T, Fujimori K.

J Obstet Gynaecol Res. 2015 Jul;41(7):1149-53. doi: 10.1111/jog.12675.

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PUBMED

[Anaesthesia for correction of scoliosis in pediatric patient with Friedreich's ataxia].

Agámez Medina GL, Pantin EJ, Lorthé J Jr, Therrien PJ.

Rev Esp Anestesiol Reanim. 2015 Jan;62(1):42-5. doi: 10.1016/j.redar.2014.03.001. English, Spanish.

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PUBMED

Motor pathway degeneration in young ataxia telangiectasia patients: A diffusion tractography study.

Sahama I, Sinclair K, Fiori S, Doecke J, Pannek K, Reid L, Lavin M, Rose S.

Neuroimage Clin. 2015 Aug 20;9:206-15. doi: 10.1016/j.nicl.2015.08.007.

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PUBMED

Friedreich's ataxia: the European consortium.

Lynch DR, Perlman SL.

Lancet Neurol. 2015 Feb;14(2):130-1. doi: 10.1016/S1474-4422(14)70327-8. No abstract available.

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