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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

3379 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Monogenic Causes of Dystonic Syndromes: Common in Dystonic Cerebral Palsy, Rare in Isolated Dystonia

Lange LM, Klein C.

Mov Disord. 2020 Dec 7. doi: 10.1002/mds.28420. Online ahead of print.

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The first case of Cri du Chat syndrome with dystonia

Moghadas F, Habibi S, Modara F, Shahidi GA, Zorzi G, Moghaddasi M, Lotfi T, Mehdizadeh M.

Clin Neurol Neurosurg. 2020 Dec 31;201:106459. doi: 10.1016/j.clineuro.2020.106459. Online ahead of print.

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Evaluation of improvement in quality of life after acupuncture in a patient with cervical dystonia: a case report

Horibe G, Yamaguchi S, Kikuchi T, Kubo A, Kouchi A, Isobe H, Araki N.

Acupunct Med. 2020 Dec 16:964528420958721. doi: 10.1177/0964528420958721. Online ahead of print.

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Deep brain stimulation procedure complicated by spontaneously resolved pneumothorax in a patient with cervical dystonia

Sobstyl M, Stapińska-Syniec A, Rylski M.

Neurol Neurochir Pol. 2020 Dec 4. doi: 10.5603/PJNNS.a2020.0091. Online ahead of print.

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SVA insertion in X-linked Dystonia Parkinsonism alters histone H3 acetylation associated with TAF1 gene

Petrozziello T, Dios AM, Mueller KA, Vaine CA, Hendriks WT, Glajch KE, Mills AN, Mangkalaphiban K, Penney EB, Ito N, Fernandez-Cerado C, Legarda GPA, Velasco-Andrada MS, Acuña PJ, Ang MA, Muñoz EL, Di

PLoS One. 2020 Dec 14;15(12):e0243655. doi: 10.1371/journal.pone.0243655. eCollection 2020.

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Precocious puberty in a girl with 3-methylglutaconic aciduria type 1 (3-MGA-I) due to a novel AUH gene mutation

Bizjak N, Zerjav Tansek M, Avbelj Stefanija M, Repic Lampret B, Mezek A, Drole Torkar A, Battelino T, Groselj U.

Mol Genet Metab Rep. 2020 Dec 2;25:100691. doi: 10.1016/j.ymgmr.2020.100691. eCollection 2020 Dec.

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Improvement in Quality of Life with OnabotulinumtoxinA for Cervical Dystonia: POSTURe

Petitclerc M, Cloutier M, Naud P, Langlois M, Bhogal M, Davidovic G.

Can J Neurol Sci. 2020 Dec 21:1-29. doi: 10.1017/cjn.2020.275. Online ahead of print.

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The Extreme Ends of the Treatment Response Spectrum to Botulinum Toxin in Cervical Dystonia

Samadzadeh S, Brauns R, Hefter H.

Toxins (Basel). 2020 Dec 31;13(1):E22. doi: 10.3390/toxins13010022.

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Reply to "Truncating VPS16 Mutations are Rare in Early-Onset Dystonia"

Zech M, Steel D, Kurian MA, Winkelmann J.

Ann Neurol. 2020 Dec 11. doi: 10.1002/ana.25988. Online ahead of print.

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Quantitative laryngeal electromyography parameters may correlate with improved outcomes following botulinum toxin injection for spasmodic dysphonia

Dwyer CD, Leclerc AA, Nandedkar SD, Young VN, Rosen CA.

Muscle Nerve. 2020 Dec 31. doi: 10.1002/mus.27161. Online ahead of print.

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Targeting pain in the long-term treatment of cervical dystonia with botulinum toxin A

Marciniec M, Szczepańska-Szerej A, Papuć E, Rejdak K.

Int J Neurosci. 2020 Dec 17:1-5. doi: 10.1080/00207454.2020.1860039. Online ahead of print.

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Contralateral C7 nerve transfer via the prespinal route in treatment of spastic paralysis of upper limb after cerebral palsy

Pan X, Zhao G, Yang X, Hua Y, Wang J, Ying Q, Mi J.

Br J Neurosurg. 2020 Dec 16:1-5. doi: 10.1080/02688697.2020.1859091. Online ahead of print.

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Functional motor disorders associated with other neurological diseases: Beyond the boundaries of "organic" neurology

Tinazzi M, Geroin C, Erro R, Marcuzzo E, Cuoco S, Ceravolo R, Mazzucchi S, Pilotto A, Padovani A, Romito LM, Eleopra R, Zappia M, Nicoletti A, Dallocchio C, Arbasino C, Bono F, Pascarella A, Demartini

Eur J Neurol. 2020 Dec 9. doi: 10.1111/ene.14674. Online ahead of print.

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Truncating VPS16 Mutations Are Rare in Early Onset Dystonia

Pott H, Brüggemann N, Reese R, Zeuner KE, Gandor F, Gruber D; DysTract Study Group, Klein C, Volkmann J, Lohmann K.

Ann Neurol. 2020 Dec 11. doi: 10.1002/ana.25990. Online ahead of print.

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Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype

Au LWC, Lee HHC, Sheng B, Chan KY, Yau EKC, Mak CM, Chan AYW, Chan AYY, Lau CKY, Mok VCT, Lam CW.

Clin Neurol Neurosurg. 2020 Dec;199:106258. doi: 10.1016/j.clineuro.2020.106258. Epub 2020 Sep 30.

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