يعرض 1 - 10 نتائج من 53 نتيجة بحث عن '"Jean‐Marc Burgunder"', وقت الاستعلام: 1.57s تنقيح النتائج
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    المصدر: NeuroImage : Clinical
    Kübel, S, Stegmayer, K, Vanbellingen, T, Pastore-Wapp, M, Bertschi, M, Burgunder, J-M, Abela, E, Weder, B, Walther, S & Bohlhalter, S 2017, ' Altered praxis network underlying limb kinetic apraxia in Parkinson's disease : an fMRI study ', NeuroImage: Clinical . https://doi.org/10.1016/j.nicl.2017.07.007Test
    Kübel, Stefanie; Stegmayer, Katharina; Vanbellingen, Tim; Pastore-Wapp, Manuela; Bertschi, Manuel; Burgunder, Jean-Marc; Abela, Eugenio; Weder, Bruno; Walther, Sebastian; Bohlhalter, Stephan (2017). Altered praxis network underlying limb kinetic apraxia in Parkinson's disease-an fMRI study. NeuroImage: Clinical, 16, pp. 88-97. Elsevier 10.1016/j.nicl.2017.07.007 <http://dx.doi.org/10.1016/j.nicl.2017.07.007Test>
    NeuroImage: Clinical, Vol 16, Iss, Pp 88-97 (2017)

    وصف الملف: application/pdf

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    المساهمون: University of Zurich, Lachenmayer, M L

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    المصدر: Brockington, Martin; Yuva, Yeliz; Prandini, Paola; Brown, Susan C.; Torelli, Silvia; Benson, Matthew A.; Herrmann, Ralf; Anderson, Louise V.B.; Bashir, Rumaisa; Burgunder, Jean-Marc; Fallet, Shari; Romero, Norma; Fardeau, Michel; Straub, Volker; Storey, Gillian; Pollitt, Christine; Richard, Isabelle; Sewry, Caroline A.; Bushby, Kate; Voit, Thomas; ... (2001). Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Human molecular genetics, 10(25), pp. 2851-2859. Oxford University Press 10.1093/hmg/10.25.2851 <http://dx.doi.org/10.1093/hmg/10.25.2851Test>

    وصف الملف: application/pdf