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PUBMED FOR HANDHELDS

Journal Abstract Search


237 related items for PubMed ID: 23219306

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  • 2. Electrophysiological evaluation of spinocerebellar ataxias 1, 2 and 3.
    Yadav R, Pal PK, Krishna N, Amar BR, Jain S, Purushottam M.
    J Neurol Sci; 2012 Jan 15; 312(1-2):142-5. PubMed ID: 21880333
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  • 6. Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxias.
    Álvarez-Paradelo S, García A, Infante J, Berciano J.
    Neurologia; 2011 Apr 15; 26(3):157-65. PubMed ID: 21163215
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  • 7. Spinocerebellar ataxias type 1, 2 and 3: a study of heart rate variability.
    Pradhan C, Yashavantha BS, Pal PK, Sathyaprabha TN.
    Acta Neurol Scand; 2008 May 15; 117(5):337-42. PubMed ID: 18028243
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  • 8. Electrophysiological features of central motor conduction in spinocerebellar atrophy type 1, type 2, and Machado-Joseph disease.
    Yokota T, Sasaki H, Iwabuchi K, Shiojiri T, Yoshino A, Otagiri A, Inaba A, Yuasa T.
    J Neurol Neurosurg Psychiatry; 1998 Oct 15; 65(4):530-4. PubMed ID: 9771779
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  • 11. Prolonged central motor conduction time of lower limb muscle in spinocerebellar ataxia 6.
    Chen JT, Lin YY, Lee YC, Soong BW, Wu ZA, Liao KK.
    J Clin Neurosci; 2004 May 15; 11(4):381-3. PubMed ID: 15080952
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  • 12. Abnormal corticospinal tract function and motor cortex excitability in non-ataxic SCA2 mutation carriers: A TMS study.
    Velázquez-Pérez L, Rodríguez-Labrada R, Torres-Vega R, Medrano Montero J, Vázquez-Mojena Y, Auburger G, Ziemann U.
    Clin Neurophysiol; 2016 Aug 15; 127(8):2713-2719. PubMed ID: 27417041
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  • 13. Cortical silent period prolongation in spinocerebellar ataxia type 2 (SCA2).
    Restivo DA, Lanza S, Giuffrida S, Le Pira F, Drago MT, Di Mauro R, Palmeri A, Puzzo D, Di Bella P, Sessa E, Rifici C, D'Aleo G, Muscarà N, Bramanti P.
    Funct Neurol; 2004 Aug 15; 19(1):37-41. PubMed ID: 15212115
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  • 15. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
    Schmitz-Hübsch T, Coudert M, Bauer P, Giunti P, Globas C, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de Warrenburg BP, Dürr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schöls L, Zdienicka E, Kang JS, Döhlinger S, Kremer B, Stephenson DA, Melegh B, Pandolfo M, di Donato S, du Montcel ST, Klockgether T.
    Neurology; 2008 Sep 23; 71(13):982-9. PubMed ID: 18685131
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  • 16. Progression of corticospinal tract dysfunction in pre-ataxic spinocerebellar ataxia type 2: A two-years follow-up TMS study.
    Velázquez-Pérez L, Rodríguez-Labrada R, Torres-Vega R, Ortega-Sánchez R, Medrano-Montero J, González-Piña R, Vázquez-Mojena Y, Auburger G, Ziemann U.
    Clin Neurophysiol; 2018 May 23; 129(5):895-900. PubMed ID: 29550649
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  • 18. Central motor conduction time.
    Udupa K, Chen R.
    Handb Clin Neurol; 2013 May 23; 116():375-86. PubMed ID: 24112910
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  • 19. Abnormal cortical excitability in patients with spinocerebellar ataxia type 12.
    Bhattacharya A, Stezin A, Kamble N, Bhardwaj S, Yadav R, Pal PK.
    Parkinsonism Relat Disord; 2024 Mar 23; 120():106002. PubMed ID: 38219530
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  • 20. [Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].
    Rakowicz M, Zdzienicka E, Poniatowska R, Waliniowska E, Sułek A, Jakubowska T, Niedzielska K, Rola R, Wierzbicka A, Hoffman-Zacharska D, Głazowski C, Jakubczyk T, Niewiadomska M, Zaremba J.
    Neurol Neurochir Pol; 2005 Mar 23; 39(4):263-275. PubMed ID: 16096942
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