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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.

Ataxia

408 ARTíCULOS , VIENDO DEL 106 AL 120

PUBMED

Innovative and effective immunosuppressive bitherapy for an unusual paraneoplastic opsoclonus-myoclonus-ataxia syndrome of the adult.

León Ruiz M, Benito-León J, García-Soldevilla MA, Rubio-Pérez L, Parra Santiago A, Lozano García-Caro LA, Izquierdo Esteban L, Hernández Martínez AC, González Estecha A, García-Albea Ristol E.

Neurologia. 2015 Jun 7. pii: S0213-4853(15)00086-9. doi: 10.1016/j.nrl.2015.02.005. [Epub ahead of print] English, Spanish. No abstract available.

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PUBMED

Phenotypic Screening for Friedreich Ataxia Using Random shRNA Selection.

Cotticelli MG, Acquaviva F, Xia S, Kaur A, Wang Y, Wilson RB.

J Biomol Screen. 2015 Oct;20(9):1084-90. doi: 10.1177/1087057115600433.

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PUBMED

Fragile X-Associated Tremor/Ataxia Syndrome in a Man in His 30s.

Martínez-Cerdeño V, Lechpammer M, Lott A, Schneider A, Hagerman R.

JAMA Neurol. 2015 Sep;72(9):1070-3. doi: 10.1001/jamaneurol.2015.1138. No abstract available.

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PUBMED

Alkaline Ceramidase 3 Deficiency Results in Purkinje Cell Degeneration and Cerebellar Ataxia Due to Dyshomeostasis of Sphingolipids in the Brain.

Wang K, Xu R, Schrandt J, Shah P, Gong YZ, Preston C, Wang L, Yi JK, Lin CL, Sun W, Spyropoulos DD, Rhee S, Li M, Zhou J, Ge S, Zhang G, Snider AJ, Hannun YA, Obeid LM, Mao C.

PLoS Genet. 2015 Oct 16;11(10):e1005591. doi: 10.1371/journal.pgen.1005591.

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PUBMED

Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine.

Kinder S, Ossig C, Wienecke M, Beyer A, von der Hagen M, Storch A, Smitka M.

Eur J Paediatr Neurol. 2015 Jan;19(1):72-4. doi: 10.1016/j.ejpn.2014.10.005.

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PUBMED

Myoclonus in ataxia-telangiectasia.

Termsarasab P, Yang AC, Frucht SJ.

Tremor Other Hyperkinet Mov (N Y). 2015 Mar 13;5:298. doi: 10.7916/D88P5Z9X.

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PUBMED

Bilateral lower-extremity numbness and ataxia in a young female runner.

Casagranda B, Srivastava U, Heller MT.

Radiol Case Rep. 2015 Nov 6;9(3):989. doi: 10.2484/rcr.v9i3.989.

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PUBMED

The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis.

Chatterjee A, Saha S, Chakraborty A, Silva-Fernandes A, Mandal SM, Neves-Carvalho A, Liu Y, Pandita RK, Hegde ML, Hegde PM, Boldogh I, Ashizawa T, Koeppen AH, Pandita TK, Maciel P, Sarkar PS, Hazra TK

PLoS Genet. 2015 Jan 29;11(1):e1004749. doi: 10.1371/journal.pgen.1004749.

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PUBMED

Square-Wave Ocular Oscillation and Ataxia in an Anti-GAD-Positive Individual With Hypothyroidism.

Brokalaki C, Kararizou E, Dimitrakopoulos A, Evdokimidis I, Anagnostou E.

J Neuroophthalmol. 2015 Dec;35(4):390-5. doi: 10.1097/WNO.0000000000000275.

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PUBMED

Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C NARP" mutation."

Martikainen MH, Gorman GS, Goldsmith P, Burn DJ, Turnbull DM, Schaefer AM.

Mov Disord. 2015 Sep;30(10):1432-3. doi: 10.1002/mds.26358. No abstract available.

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PUBMED

Frataxin levels in peripheral tissue in Friedreich ataxia.

Lazaropoulos M, Dong Y, Clark E, Greeley NR, Seyer LA, Brigatti KW, Christie C, Perlman SL, Wilmot GR, Gomez CM, Mathews KD, Yoon G, Zesiewicz T, Hoyle C, Subramony SH, Brocht AF, Farmer JM, Wilson RB

Ann Clin Transl Neurol. 2015 Aug;2(8):831-42. doi: 10.1002/acn3.225.

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PUBMED

Myoclonic axial jerks for diagnosing atypical evolution of ataxia telangiectasia.

Nakayama T, Sato Y, Uematsu M, Takagi M, Hasegawa S, Kumada S, Kikuchi A, Hino-Fukuyo N, Sasahara Y, Haginoya K, Kure S.

Brain Dev. 2015 Mar;37(3):362-5. doi: 10.1016/j.braindev.2014.06.001.

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PUBMED

Excision of Expanded GAA Repeats Alleviates the Molecular Phenotype of Friedreich's Ataxia.

Li Y, Polak U, Bhalla AD, Rozwadowska N, Butler JS, Lynch DR, Dent SY, Napierala M.

Mol Ther. 2015 Jun;23(6):1055-65. doi: 10.1038/mt.2015.41.

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PUBMED

HIV Presenting as Cerebellar Ataxia.

Agrawal RP, Jain A, Chahar C, Sirohi P, Meel JK, Mathur G.

J Assoc Physicians India. 2015 Jun;63(6):75-7.

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PUBMED

Open-label pilot study of interferon gamma-1b in Friedreich ataxia.

Seyer L, Greeley N, Foerster D, Strawser C, Gelbard S, Dong Y, Schadt K, Cotticelli MG, Brocht A, Farmer J, Wilson RB, Lynch DR.

Acta Neurol Scand. 2015 Jul;132(1):7-15. doi: 10.1111/ane.12337.

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