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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

169 ARTíCULOS , VIENDO DEL 121 AL 135

PUBMED

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort study.

Carecchio M, Invernizzi F, Gonzàlez-Latapi P, Panteghini C, Zorzi G, Romito L, Leuzzi V, Galosi S, Reale C, Zibordi F, Joseph AP, Topf M, Piano C, Bentivoglio AR, Girotti F, Morana P, Morana B, Kurian

Mov Disord. 2019 Jun 19. doi: 10.1002/mds.27771. [Epub ahead of print]

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PUBMED

Sensory trick in upper limb dystonia.

Dagostino S, Ercoli T, Gigante AF, Pellicciari R, Fadda L, Defazio G.

Parkinsonism Relat Disord. 2019 Jan 6. pii: S1353-8020(19)30006-9. doi: 10.1016/j.parkreldis.2019.01.006. [Epub ahead of print]

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PUBMED

Management of Spastic Paresis and Cervical Dystonia: access to Therapeutic Innovations Through an International Program of Practical Courses.

Colosimo C, Bhidayasiri R, Fheodoroff K, Bhatia K, Chung TM, Landreau T, Jacinto LJ.

Clin Ther. 2019 Oct 10. pii: S0149-2918(19)30484-9. doi: 10.1016/j.clinthera.2019.09.007. [Epub ahead of print]

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PUBMED

No Evidence for Dystonia-Like Sensory Overflow of Tongue Representations in Adults Who Stutter.

Vreeswijk SME, Hoang TNL, Korzeczek A, Neef NE, Wolff von Gudenberg A, Paulus W, Sommer M.

Front Hum Neurosci. 2019 Oct 4;13:336. doi: 10.3389/fnhum.2019.00336. eCollection 2019.

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PUBMED

Intracranial calcifications and dystonia associated with a novel deletion of chromosome 8p11.2 encompassing SLC20A2 and THAP1.

Mu W, Tochen L, Bertsch C, Singer HS, Barañano KW.

BMJ Case Rep. 2019 May 27;12(5). pii: e228782. doi: 10.1136/bcr-2018-228782.

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PUBMED

A Case of Ascending and Descending Stair-Specific Dystonia.

Arceri T, Ratliff J.

J Mov Disord. 2019 Apr 5. doi: 10.14802/jmd.18057. [Epub ahead of print] No abstract available.

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PUBMED

Functional and structural neural bases of task specificity in isolated focal dystonia.

Bianchi S, Fuertinger S, Huddleston H, Frucht SJ, Simonyan K.

Mov Disord. 2019 Mar 6. doi: 10.1002/mds.27649. [Epub ahead of print]

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PUBMED

Pain in cervical dystonia and the antinociceptive effects of botulinum toxin: what is currently known?

Marciniec M, Szczepańska-Szerej A, Kulczyński M, Sapko K, Popek-Marciniec S, Rejdak K.

Rev Neurosci. 2019 Mar 27. pii: /j/revneuro.ahead-of-print/revneuro-2018-0119/revneuro-2018-0119.xml. doi: 10.1515/revneuro-2018-0119. [Epub ahead of print]

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PUBMED

Evaluation of anxiety and depression scales and quality of LIFE in cervical dystonia patients on botulinum toxin therapy and their relatives.

Ceylan D, Erer S, Zarifoğlu M, Türkeş N, Özkaya G.

Neurol Sci. 2019 Jan 18. doi: 10.1007/s10072-019-3719-9. [Epub ahead of print]

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PUBMED

Persistence of limb dystonia and myoclonus during sleep in corticobasal syndrome: a case series.

Infante R, Antelmi E, Pizza F, Stanzani Maserati M, Plazzi G, Rizzo G, Liguori R.

Sleep Med. 2019 Jul;59:107-109. doi: 10.1016/j.sleep.2018.12.025. Epub 2019 Feb 2. No abstract available.

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PUBMED

[KMT2B variants responsible for children dystonia 28: report of two cases].

Dai LF, Ding CH, Fang T, Xie ZH, Liu TH, Zhang WH, Wang XH, Ren XT, Liu M, Tian XJ, Wu HS, Fang F.

Zhonghua Er Ke Za Zhi. 2019 Jul 2;57(7):564-566. doi: 10.3760/cma.j.issn.0578-1310.2019.07.015. Chinese.

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PUBMED

Abnormalities in grey matter structure in embouchure dystonia.

Mantel T, Altenmüller E, Li Y, Meindl T, Jochim A, Lee A, Zimmer C, Dresel C, Haslinger B.

Parkinsonism Relat Disord. 2019 May 7. pii: S1353-8020(19)30229-9. doi: 10.1016/j.parkreldis.2019.05.008. [Epub ahead of print]

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PUBMED

Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia.

Hellberg C, Alinder E, Jaraj D, Puschmann A.

Parkinsonism Relat Disord. 2019 Dec;69:79-84. doi: 10.1016/j.parkreldis.2019.10.028. Epub 2019 Oct 29.

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PUBMED

Epileptic Encephalopathy, Myoclonus-Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene.

Giacomini T, Vari MS, Janis S, Prato G, Pisciotta L, Rocchi A, Michelucci A, Di Rocco M, Gandullia P, Mattioli G, Sacco O, Morana G, Mancardi MM.

Neuropediatrics. 2019 Oct;50(5):327-331. doi: 10.1055/s-0039-1692141. Epub 2019 Jul 18.

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PUBMED

A hexanucleotide repeat modifies expressivity of X-linked dystonia-parkinsonism.

Westenberger A, Reyes CJ, Saranza G, Dobricic V, Hanssen H, Domingo A, Laabs BH, Schaake S, Pozojevic J, Rakovic A, Grütz K, Begemann K, Walter U, Dressler D, Bauer P, Rolfs A, Münchau A, Kaiser FJ, O

Ann Neurol. 2019 Apr 11. doi: 10.1002/ana.25488. [Epub ahead of print]

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