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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 31 AL 45

PUBMED

[Diagnosis of Spinocerebellar Ataxia type 3 (Machado-Joseph disease) in Chile].

Miranda C M.

Rev Med Chil. 2015 Jan;143(1):126-7. doi: 10.4067/S0034-98872015000100019. Spanish. No abstract available.

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Spontaneous downbeat nystagmus as a clue for the diagnosis of ataxia associated with anti-GAD antibodies.

Vale TC, Pedroso JL, Alquéres RA, Dutra LA, Barsottini OG.

J Neurol Sci. 2015 Dec 15;359(1-2):21-3. doi: 10.1016/j.jns.2015.10.024.

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Spinocerebellar ataxia-10 with paranoid schizophrenia.

Trikamji B, Singh P, Mishra S.

Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):93-5. doi: 10.4103/0972-2327.144285.

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Vision related quality of life in spinocerebellar ataxia.

Kedar S, Ghate D, Murray EL, Corbett JJ, Subramony SH.

J Neurol Sci. 2015 Nov 15;358(1-2):404-8. doi: 10.1016/j.jns.2015.10.013.

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Neuro-Ophthalmological Findings in Children and Adolescents with Chronic Ataxia.

Salman MS, Chodirker BN.

Neuroophthalmology. 2015 Jun 17;39(3):125-131.

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A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds.

Rohdin C, Gilliam D, O'Leary CA, O'Brien DP, Coates JR, Johnson GS, Jäderlund KH.

Acta Vet Scand. 2015 May 23;57:26. doi: 10.1186/s13028-015-0115-1.

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Two novel mutations of the SETX gene and ataxia with oculomotor apraxia type 2.

Pera J, Lechner S, Biskup S, Strach M, Grodzicki T, Slowik A.

Clin Neurol Neurosurg. 2015 Jan;128:44-6. doi: 10.1016/j.clineuro.2014.10.024. No abstract available.

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[Spinocerebellar ataxia type 3 (Machado-Joseph disease) and varenicline].

Young P, Finn BC, Giuliani F, Reisin R.

Rev Med Chil. 2015 Sep;143(9):1221-2. doi: 10.4067/S0034-98872015000900019. Spanish. No abstract available.

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Excessive brain iron accumulation in spinocerebellar ataxia type 17.

Claassen J, Gerding WM, Kastrup O, Uslar E, Goericke S, Timmann D.

Neurology. 2015 Jan 13;84(2):212-3. doi: 10.1212/WNL.0000000000001141. No abstract available.

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Hypermetabolism of Olivary Nuclei in a Patient with Progressive Ataxia and Palatal Tremor.

Korpela J, Joutsa J, Rinne JO, Bergman J, Kaasinen V.

Tremor Other Hyperkinet Mov (N Y). 2015 Aug 31;5:342. doi: 10.7916/D8PV6JMT.

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Nasality in Friedreich ataxia.

Poole ML, Wee JS, Folker JE, Corben LA, Delatycki MB, Vogel AP.

Clin Linguist Phon. 2015 Jan;29(1):46-58. doi: 10.3109/02699206.2014.954734.

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TPP1 deficiency: Rare cause of isolated childhood-onset progressive ataxia.

Dy ME, Sims KB, Friedman J.

Neurology. 2015 Oct 6;85(14):1259-61. doi: 10.1212/WNL.0000000000001876. No abstract available.

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Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12.

O'Hearn EE, Hwang HS, Holmes SE, Rudnicki DD, Chung DW, Seixas AI, Cohen RL, Ross CA, Trojanowski JQ, Pletnikova O, Troncoso JC, Margolis RL.

Mov Disord. 2015 Nov;30(13):1813-24. doi: 10.1002/mds.26348.

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The mechanism of ipsilateral ataxia in lacunar hemiparesis: SPECT perfusion imaging.

Yamamoto R, Johkura K, Nakae Y, Tanaka F.

Eur Neurol. 2015;73(1-2):106-11. doi: 10.1159/000369009.

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