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.
Tema
2013
4639 ARTíCULOS , VIENDO DEL 1 AL 15
Parkinson's disease: strong marriages suffer more.
Tellis-Nayak V.
Provider. 2013 Dec;39(12):35-6. No abstract available.
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Genetics in dystonia: an update.
Fuchs T, Ozelius LJ.
Curr Neurol Neurosci Rep. 2013 Dec;13(12):410. doi: 10.1007/s11910-013-0410-z. Review.
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Swarup V, Srivastava AK, Padma MV, Rajeswari MR.
J Neurosci Res. 2013 Nov;91(11):1483-91. doi: 10.1002/jnr.23262.
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Genetic variants ofLRRK2 in Taiwanese Parkinson's disease.
Wu YR, Chang KH, Chang WT, Hsiao YC, Hsu HC, Jiang PR, Chen YC, Chao CY, Chang YC, Lee BH, Hu FJ, Chen WL, Lee-Chen GJ, Chen CM.
PLoS One. 2013 Dec 5;8(12):e82001. doi: 10.1371/journal.pone.0082001.
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Tremor associated with focal and segmental dystonia.
Rudzińska M, Krawczyk M, Wójcik-Pędziwiatr M, Szczudlik A, Wasielewska A.
Neurol Neurochir Pol. 2013 May-Jun;47(3):223-31.
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Origin of the spinocerebellar ataxia type 7 gene mutation in Mexican population.
Magaña JJ, Gómez R, Maldonado-Rodríguez M, Velázquez-Pérez L, Tapia-Guerrero YS, Cortés H, Leyva-García N, Hernández-Hernández O, Cisneros B.
Cerebellum. 2013 Dec;12(6):902-5. doi: 10.1007/s12311-013-0505-8.
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Mapping of the PDQ-39 to EQ-5D scores in patients with Parkinson's disease.
Young MK, Ng SK, Mellick G, Scuffham PA.
Qual Life Res. 2013 Jun;22(5):1065-72. doi: 10.1007/s11136-012-0231-6.
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Acute dystonia after using single dose duloxetine: case report.
Karakaş Uğurlu G, Onen S, Bayındırlı D, Cayköylü A.
Psychiatry Investig. 2013 Mar;10(1):95-7. doi: 10.4306/pi.2013.10.1.95.
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Ataxia-telangiectasia and wilms tumor: reduced treatment but early relapse.
Pérez-Villena A, Cormenzana M, de Prada I, Pérez-Martínez A, Aleo E.
J Pediatr Hematol Oncol. 2013 May;35(4):308-10. doi: 10.1097/MPH.0b013e31828fccdf.
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Axon degeneration in Parkinson's disease.
Burke RE, O'Malley K.
Exp Neurol. 2013 Aug;246:72-83. doi: 10.1016/j.expneurol.2012.01.011. Review.
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Doxycycline restrains glia and confers neuroprotection in a 6-OHDA Parkinson model.
Lazzarini M, Martin S, Mitkovski M, Vozari RR, Stühmer W, Bel ED.
Glia. 2013 Jul;61(7):1084-100. doi: 10.1002/glia.22496.
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Magnetization transfer imaging in premanifest and manifest huntington disease: a 2-year follow-up.
van den Bogaard SJ, Dumas EM, Hart EP, Milles J, Reilmann R, Stout JC, Craufurd D, Gibbard CR, Tabrizi SJ, van Buchem MA, van der Grond J, Roos RA.
AJNR Am J Neuroradiol. 2013 Feb;34(2):317-22. doi: 10.3174/ajnr.A3303.
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Strategies used by teens growing up in families with Huntington disease.
Williams JK, Driessnack M, Barnette JJ, Sparbel KJ, Leserman A, Thompson S, Paulsen JS.
J Pediatr Nurs. 2013 Sep-Oct;28(5):464-9. doi: 10.1016/j.pedn.2013.02.030.
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Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease.
Izumi Y, Miyamoto R, Morino H, Yoshizawa A, Nishinaka K, Udaka F, Kameyama M, Maruyama H, Kawakami H.
Neurology. 2013 Feb 5;80(6):600-1. doi: 10.1212/WNL.0b013e3182815529. No abstract available. Erratum in: Neurology. 2013 Mar 26;80(13):1267.
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Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease.
Kim JS, Son TO, Youn J, Ki CS, Cho JW.
J Clin Neurol. 2013 Oct;9(4):274-9. doi: 10.3988/jcn.2013.9.4.274.
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