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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

753 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Childhood-onset progressive dystonia associated with pathogenic truncating variants in CHD8

Doummar D, Treven M, Qebibo L, Devos D, Ghoumid J, Ravelli C, Kranz G, Krenn M, Demailly D, Cif L, Davion JB, Zimprich F, Burglen L, Zech M.

Ann Clin Transl Neurol. 2021 Oct;8(10):1986-1990. doi: 10.1002/acn3.51444. Epub 2021 Aug 20.

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Anti-N-methyl-D-aspartate receptor encephalitis: An observational and comparative study in Mexican children and adults

Herrera-Mora P, Munive-Baez L, Ruiz García M, Galindo-Martínez A, Maldonado-Diaz DE, Delgado RD, Cárdenas G.

Clin Neurol Neurosurg. 2021 Oct 11;210:106986. doi: 10.1016/j.clineuro.2021.106986. Online ahead of print.

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Clozapine-Associated Pisa Syndrome: A Case Report of an Acute Reaction in a Bipolar Patient

Santos HC, Oliveira J, Vieira AS, Pereira J.

Clin Neuropharmacol. 2021 Oct 12. doi: 10.1097/WNF.0000000000000485. Online ahead of print.

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Intrathecal Baclofen Pump Infection With Meningitis: Effective Treatment by Radical Debridement and Intrareservoir Baclofen-Vancomycin Co-Infusion

Koljonen PA, Chan SHS, Liu T, Ho ACC, Chim S, Tsoi NS, Wong YW.

Neuromodulation. 2021 Oct;24(7):1223-1228. doi: 10.1111/ner.13369. Epub 2021 Feb 3.

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Duration and onset of effect of incobotulinumtoxinA for the treatment of blepharospasm in botulinum toxin-naïve subjects

Mitsikostas DD, Dekundy A, Hanschmann A, Althaus M, Scheschonka A, Pagan F, Jankovic J.

Curr Med Res Opin. 2021 Oct;37(10):1761-1768. doi: 10.1080/03007995.2021.1965975. Epub 2021 Aug 24.

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A Novel Homozygous ADCY5 Variant is Associated with a Neurodevelopmental Disorder and Movement Abnormalities

Kaiyrzhanov R, Zaki MS, Maroofian R, Dominik N, Rad A, Vona B, Houlden H.

Mov Disord Clin Pract. 2021 Jul 31;8(7):1140-1143. doi: 10.1002/mdc3.13310. eCollection 2021 Oct.

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Generation of two induced pluripotent stem cell lines with heterozygous and homozygous GAG deletion in TOR1A gene from a healthy hiPSC line

Akter M, Cui H, Chen YH, Ding B.

Stem Cell Res. 2021 Oct;56:102536. doi: 10.1016/j.scr.2021.102536. Epub 2021 Sep 11.

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Moyamoya disease: a spectrum of clinical and radiological findings in a series of eight paediatric patients

Malakar S, Datta AK, Chakraborty U, Chaudhury J, Kumar S, Chandra A, Ray BK.

Acta Neurol Belg. 2021 Oct;121(5):1165-1172. doi: 10.1007/s13760-021-01604-6. Epub 2021 Feb 4.

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Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations

Baviera-Muñoz R, Campins-Romeu M, Carretero-Vilarroig L, Sastre-Bataller I, Martínez-Torres I, Vázquez-Costa JF, Muelas N, Sevilla T, Vílchez JJ, Aller E, Jaijo T, Bataller L, Espinós C.

J Neurol Sci. 2021 Oct 15;429:118062. doi: 10.1016/j.jns.2021.118062. Epub 2021 Aug 30.

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Teaching Video NeuroImage: New STUB1 Variant Causes Chorea, Tremor, Dystonia, Myoclonus, Ataxia, Depression, Cognitive Impairment, Epilepsy, and Superficial Siderosis

Saft C, Skodda S, Nguyen HP, Park J, Haack TB.

Neurology. 2021 Oct 26;97(17):e1749-e1750. doi: 10.1212/WNL.0000000000012264. Epub 2021 May 26.

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PUBMED

Outcomes of a regional variant of botulinum toxin type A in the treatment of essential blepharospasm and hemifacial spasms: A retrospective study

Maneksha V, Chakrabarty S, Tanwar M, Pillai MR.

Indian J Ophthalmol. 2021 Oct;69(10):2777-2781. doi: 10.4103/ijo.IJO_3656_20.

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Acute Extrapyramidal Side Effects from Smoked Haloperidol

Pham A, Lee JY, Miller CWT.

Case Rep Psychiatry. 2021 Oct 2;2021:4177263. doi: 10.1155/2021/4177263. eCollection 2021.

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Chronic form of Pisa syndrome after prolonged exposure to low-dose amisulpride treatment

Erdem NŞ, Özkaynak SS.

Ideggyogy Sz. 2021 Sep 30;74(9-10):356-360. doi: 10.18071/isz.74.0356.

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Rechargeable Pacemaker Technology in Deep Brain Stimulation: A Step Forward, But Not for Everyone

Runge J, Nagel JM, Schrader C, Saryyeva A, Krauss JK.

Mov Disord Clin Pract. 2021 Aug 13;8(7):1112-1115. doi: 10.1002/mdc3.13306. eCollection 2021 Oct.

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A pathogenic DYT-THAP1 dystonia mutation causes hypomyelination and loss of YY1 binding

Yellajoshyula D, Rogers AE, Kim AJ, Kim S, Pappas SS, Dauer WT.

Hum Mol Genet. 2021 Oct 23:ddab310. doi: 10.1093/hmg/ddab310. Online ahead of print.

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