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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

276 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Early Illustrations of Geste Antagoniste in Cervical and Generalized Dystonia.

Broussolle E, Laurencin C, Bernard E, Thobois S, Danaila T, Krack P.

Tremor Other Hyperkinet Mov (N Y). 2015 Sep 21;5:332. doi: 10.7916/D8KD1X74. Review.

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Steroid-responsive autoimmune encephalopathy associated with autoimmune thyroiditis (SREAT) presenting with myoclonus-dystonia syndrome.

Rožanković PB, Rožanković M, Šušak I, Vlahović I, Sporis D.

J Neurol Sci. 2015 Jul 15;354(1-2):110-1. doi: 10.1016/j.jns.2015.04.021. Review. No abstract available. Erratum in: J Neurol Sci. 2015 Sep 15;356(1-2):219. Rožanković, Marjan [added]; Šušak, Ivana [added]; Vlahović, Ivan [added]; Sporis, Davor [added].

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PUBMED

Deep brain stimulation and dantrolene for secondary dystonia in x-linked adrenoleukodystrophy.

van Karnebeek C, Horvath G, Murphy T, Purtzki J, Bowden K, Sirrs S, Honey CR, Stockler S.

JIMD Rep. 2015;15:113-6. doi: 10.1007/8904_2014_305.

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PUBMED

Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia.

Zech M, Lam DD, Francescatto L, Schormair B, Salminen AV, Jochim A, Wieland T, Lichtner P, Peters A, Gieger C, Lochmüller H, Strom TM, Haslinger B, Katsanis N, Winkelmann J.

Am J Hum Genet. 2015 Jun 4;96(6):883-93. doi: 10.1016/j.ajhg.2015.04.010.

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PUBMED

DYT2 revealed: Hippocalcin mutations cause autosomal-recessive isolated dystonia.

Erro R, Klein C.

Mov Disord. 2015 Nov;30(13):1725. doi: 10.1002/mds.26280. Review. No abstract available.

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PUBMED

Interventional studies in childhood dystonia do not address the concerns of children and their carers.

Lumsden DE, Gimeno H, Tustin K, Kaminska M, Lin JP.

Eur J Paediatr Neurol. 2015 May;19(3):327-36. doi: 10.1016/j.ejpn.2015.01.003.

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PUBMED

[A case of 16q linked autosomal dominant cerebellar ataxia (16q-ADCA) presenting dystonia].

Sugawara M, Kamada S, Toyoshima I.

Rinsho Shinkeigaku. 2015;55(6):432-3. doi: 10.5692/clinicalneurol.cn-000653. Japanese. No abstract available.

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PUBMED

Facial dystonia as depicted in art in the time of Leonardo da Vinci.

Bono F, Morelli M, Quattrone A.

Lancet Neurol. 2015 Apr;14(4):351. doi: 10.1016/S1474-4422(15)70012-8. No abstract available.

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PUBMED

Development of the Comprehensive Cervical Dystonia Rating Scale: Methodology.

Comella CL, Fox SH, Bhatia KP, Perlmutter JS, Jinnah HA, Zurowski M, McDonald WM, Marsh L, Rosen AR, Waliczek T, Wright LJ, Galpern WR, Stebbins GT.

Mov Disord Clin Pract. 2015 Jun;2(2):135-141.

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Mixed effectiveness of rTMS and retraining in the treatment of focal hand dystonia.

Kimberley TJ, Schmidt RL, Chen M, Dykstra DD, Buetefisch CM.

Front Hum Neurosci. 2015 Jul 9;9:385. doi: 10.3389/fnhum.2015.00385.

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PUBMED

Myoclonus-dystonia syndrome: case report.

Akarsu EO, Surmeli R, Yalcin D.

North Clin Istanb. 2015 Jan 24;1(3):187-190. doi: 10.14744/nci.2014.28247.

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Val66Met polymorphism of brain-derived neurotrophic factor is associated with idiopathic dystonia.

Sako W, Murakami N, Izumi Y, Kaji R.

J Clin Neurosci. 2015 Mar;22(3):575-7. doi: 10.1016/j.jocn.2014.08.014.

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PUBMED

Oromandibular dystonia: a serious side effect of capecitabine.

van Pelt-Sprangers MJ, Geijteman EC, Alsma J, Boere IA, Mathijssen RH, Schuit SC.

BMC Cancer. 2015 Mar 11;15:115. doi: 10.1186/s12885-015-1132-1.

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PUBMED

Hairdresser dystonia: an unusual substantia nigra hyperechogenicity.

Yoo SW, Park HE, Lee KS, Kim JS.

J Neurol Sci. 2015 Oct 15;357(1-2):314-6. doi: 10.1016/j.jns.2015.07.029. No abstract available.

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PUBMED

Eating dystonia in a case of neuroacanthocytosis.

Rohani M, Shahidi G.

Iran J Neurol. 2015 Jan 5;14(1):52. No abstract available.

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