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Diagnostic accuracy of diffusion tensor imaging in amyotrophic lateral sclerosis: a systematic review and individual patient data meta-analysis. by Foerster, B, Dwamena, B, Petrou, M, Carlos, R, Callaghan, B, Churchill, C, Mohamed, M, Bartels, C, Benatar, M, Bonzano, L, Ciccarelli, O, Cosottini, M, Ellis, C, Ehrenreich, H, Filippini, N, Ito, M, Kalra, S, Melhem, E, Pyra, T, Roccatagliata, L, Senda, J, Sobue, G, Turner, M, Feldman, E, Pomper, MG
Published 2013Journal article -
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Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy by Park, J, Tucci, A, Cipriani, V, Demidov, G, Rocca, C, Senderek, J, Butryn, M, Velic, A, Lam, T, Galanaki, E, Cali, E, Vestito, L, Maroofian, R, Deininger, N, Rautenberg, M, Admard, J, Hahn, G-A, Bartels, C, van Os, NJH, Horvath, R, Chinnery, PF, Tiet, MY, Hewamadduma, C, Hadjivassiliou, M, Tofaris, GK, Genomics England Research Consortium, Wood, NW, Hayer, SN, Bender, F, Menden, B, Cordts, I, Klein, K, Nguyen, HP, Krauss, JK, Blahak, C, Strom, TM, Sturm, M, van de Warrenburg, B, Lerche, H, Maček, B, Synofzik, M, Ossowski, S, Timmann, D, Wolf, ME, Smedley, D, Riess, O, Schöls, L, Houlden, H, Haack, TB, Hengel, H
Published 2022Journal article