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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.

Distonía

317 ARTíCULOS , VIENDO DEL 301 AL 315

PUBMED

Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia.

Cai X, Chen X, Wu S, Liu W, Zhang X, Zhang D, He S, Wang B, Zhang M, Zhang Y, Li Z, Luo K, Cai Z, Li W.

Sci Rep. 2016 May 12;6:25834. doi: 10.1038/srep25834.

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PUBMED

Dystonia-Causing Mutations as a Contribution to the Etiology of Spasmodic Dysphonia.

de Gusmão CM, Fuchs T, Moses A, Multhaupt-Buell T, Song PC, Ozelius LJ, Franco RA, Sharma N.

Otolaryngol Head Neck Surg. 2016 Oct;155(4):624-8. doi: 10.1177/0194599816648293.

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PUBMED

Erratum to: Strategies for treatment of dystonia.

Dressler D, Altenmueller E, Bhidayasiri R, Bohlega S, Chana P, Chung TM, Frucht S, Garcia-Ruiz PJ, Kaelin A, Kaji R, Kanovsky P, Laskawi R, Micheli F, Orlova O, Relja M, Rosales R, Slawek J, Timerbaev

J Neural Transm (Vienna). 2016 Mar;123(3):259. doi: 10.1007/s00702-015-1471-8. No abstract available.

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PUBMED

Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia.

Masuho I, Fang M, Geng C, Zhang J, Jiang H, Özgul RK, Yılmaz DY, Yalnızoğlu D, Yüksel D, Yarrow A, Myers A, Burn SC, Crotwell PL, Padilla-Lopez S, Dursun A, Martemyanov KA, Kruer MC.

Neurol Genet. 2016 May 12;2(3):e78. doi: 10.1212/NXG.0000000000000078. No abstract available.

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PUBMED

Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.

Tuschl K, Meyer E, Valdivia LE, Zhao N, Dadswell C, Abdul-Sada A, Hung CY, Simpson MA, Chong WK, Jacques TS, Woltjer RL, Eaton S, Gregory A, Sanford L, Kara E, Houlden H, Cuno SM, Prokisch H, Valletta

Nat Commun. 2016 May 27;7:11601. doi: 10.1038/ncomms11601.

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PUBMED

Bilateral Pallidotomy for Cervical Dystonia After Failed Selective Peripheral Denervation.

Horisawa S, Goto S, Takeda N, Terashima H, Kawamata T, Taira T.

World Neurosurg. 2016 May;89:728.e1-4. doi: 10.1016/j.wneu.2016.01.011.

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PUBMED

The shirt collar sign" of cervical dystonia."

Silver MR, Hanfelt J, Factor SA.

Int J Neurosci. 2016 Jun 2:1-3. [Epub ahead of print]

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PUBMED

Periodontal treatment in a patient with generalized idiopathic dystonia.

Zuza EP, Campos LC, Vanzelli ML, Martins AT, Pontes AE, Ribeiro FS, Toledo BE, Pires JR.

Spec Care Dentist. 2016 Jan;36(1):48-52. doi: 10.1111/scd.12144.

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PUBMED

Prevalence of Dystonia in Antioquia, Colombia.

Solano Atehortúa JM, Isaza Jaramillo SP, Rendón Bañol A, Buritica Henao O.

Neuroepidemiology. 2016;46(2):137-43. doi: 10.1159/000443834.

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PUBMED

Botulinum Toxin Treatment of Cervical Dystonia.

Bledsoe IO, Comella CL.

Semin Neurol. 2016 Feb;36(1):47-53. doi: 10.1055/s-0035-1571210. Review.

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PUBMED

Sleep in patients with primary dystonia: A systematic review on the state of research and perspectives.

Hertenstein E, Tang NK, Bernstein CJ, Nissen C, Underwood MR, Sandhu HK.

Sleep Med Rev. 2016 Apr;26:95-107. doi: 10.1016/j.smrv.2015.04.004. Review.

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PUBMED

Expanding the phenotype in aminoacylase 1 (ACY1) deficiency: characterization of the molecular defect in a 63-year-old woman with generalized dystonia.

Sass JO, Vaithilingam J, Gemperle-Britschgi C, Delnooz CC, Kluijtmans LA, van de Warrenburg BP, Wevers RA.

Metab Brain Dis. 2016 Jun;31(3):587-92. doi: 10.1007/s11011-015-9778-6.

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PUBMED

Metformin-induced acute dystonia in a schizophrenic patient treated with sulpiride and clozapine.

Chen WH, Huang WL, Hsieh MH.

Psychiatry Clin Neurosci. 2016 Aug;70(8):362-3. doi: 10.1111/pcn.12405. No abstract available.

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PUBMED

Late-onset primary dystonia in Zhejiang province of China: a service-based epidemiological study.

Wang L, Chen Y, Hu B, Hu X.

Neurol Sci. 2016 Jan;37(1):111-6. doi: 10.1007/s10072-015-2366-z.

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PUBMED

Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation.

Eggink H, van Egmond ME, Verschuuren-Bemelmans CC, Schönherr MC, de Koning TJ, Oterdoom DL, van Dijk JM, Tijssen MA.

Mov Disord. 2016 Nov 8. doi: 10.1002/mds.26842. [Epub ahead of print]

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