Topological nonmagnetic impurity states in topological Kondo insulators von Abele, M., Yuan, X., Riseborough, P. S.

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Impaired heart rate variability in cervical dystonia is associated to depression von Hentschel, F., Dressler, D., Abele, M., Paus, S.

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Solid State Nuclear Magnetic Resonance and X-ray Diffraction Line Profile Analysis of heavily deformed fluorite von Abdellatief, M., Abele, M., Leoni, M., Scardi, P.

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Voxel-based morphometry and voxel-based relaxometry in multiple system atrophy—A comparison between clinical subtypes and correlations with clinical parameters von Minnerop, M., Specht, K., Ruhlmann, J., Schimke, N., Abele, M., Weyer, A., Wüllner, U., Klockgether, T.

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Stevens Johnson syndrome without skin lesions von Latsch, K, Girschick, H. J, Abele-Horn, M

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The aetiology of sporadic adult-onset ataxia von ABELE, M, BÜRK, K, SCHÖLS, L, SCHWARTZ, S, BESENTHAL, I, DICHGANS, J, ZÜHLKE, C, RIESS, O, KLOCKGETHER, T

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Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2 von Velázquez-Pérez, L, Seifried, C, Abele, M, Wirjatijasa, F, Rodríguez-Labrada, R, Santos-Falcón, N, Sánchez-Cruz, G, Almaguer-Mederos, L, Tejeda, R, Canales-Ochoa, N, Fetter, M, Ziemann, U, Klockgether, T, Medrano-Montero, J, Rodríguez-Díaz, J, Laffita-Mesa, J.M, Auburger, G

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Sporadic adult onset ataxia of unknown etiology : A clinical, electrophysiological and imaging study von ABELE, Michael, MINNEROP, Martina, URBACH, Horst, SPECHT, Karsten, KLOCKGETHER, Thomas

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Prevalence of antigliadin antibodies in ataxia patients von ABELE, M, SCHÖLS, L, SCHWARTZ, S, KLOCKGETHER, T

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The natural history of degenerative ataxia : a retrospective study in 466 patients von KLOCKGETHER, T, LÜDTKE, R, BRICE, A, INZELBERG, R, ZILBER, N, DICHGANS, J, KRAMER, B, ABELE, M, BÜRK, K, SCHÖLS, L, RIESS, O, LACCONE, F, BOESCH, S, LOPES-CENDES, I

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Probable multiple system atrophy in a German family von Wüllner, U, Abele, M, Schmitz-Huebsch, T, Wilhelm, K, Benecke, R, Deuschl, G, Klockgether, T

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Features of probable multiple system atrophy patients identified among 4770 patients with parkinsonism enrolled in the multicentre registry of the German Competence Network on Park... von Wüllner, U., Schmitz-Hübsch, T., Abele, M., Antony, G., Bauer, P., Eggert, K.

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The European Multiple System Atrophy-Study Group (EMSA-SG) von Geser, F, Seppi, K, Stampfer-Kountchev, M, Köllensperger, M, Diem, A, Ndayisaba, J P, Ostergaard, K, Dupont, E, Cardozo, A, Tolosa, E, Abele, M, Dodel, R, Klockgether, T, Ghorayeb, I, Yekhlef, F, Tison, F, Daniels, C, Kopper, F, Deuschl, G, Coelho, M, Ferreira, J, Rosa, M M, Sampaio, C, Bozi, M, Schrag, A, Hooker, J, Kim, H, Scaravilli, T, Mathias, C J, Fowler, C, Wood, N, Quinn, N, Widner, H, Nilsson, C F, Lindvall, O, Schimke, N, Eggert, K M, Oertel, W, del Sorbo, F, Carella, F, Albanese, A, Pellecchia, M T, Barone, P, Djaldetti, R, Meco, G, Colosimo, C, Gonzalez-Mandly, A, Berciano, J, Gurevich, T, Giladi, N, Galitzky, M, Ory, F, Rascol, O, Kamm, C, Buerk, K, Maass, S, Gasser, T, Poewe, W, Wenning, G K

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Autosomal dominant cerebellar ataxia type I Clinical features and MRI in families with SCA1, SCA2 and SCA3 von Bürk, K., Abele, M., Fetter, M., Dichgans, J., Skalej, M., Laccone, F., Didierjean, O., Brice, A., Klockgether, T.

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Autosomal dominant cerebellar ataxia type I : oculomotor abnormalities in families with SCA1, SCA2, and SCA3 von BÜRK, K, FETTER, M, ABELE, M, LACCONE, F, BRICE, A, DICHGANS, J, KLOCKGETHER, T

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Autosomal dominant cerebellar ataxia type I : MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3 von KLOCKGETHER, T, SKALEJ, M, DICHGANS, J, WEDEKIND, D, LUFT, A. R, WELTE, D, SCHULZ, J. B, ABELE, M, BÜRK, K, LACCONE, F, BRICE, A

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Cerebellar ataxia with glutamic acid decarboxylase autoantibodies von ABELE, M, WELLER, M, MESCHERIAKOV, S, BÜRK, K, DICHGANS, J, KLOCKGETHER, T

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Generation and confinement of uniform magnetic fields with surface currents von Abele, M.G.

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L-carnitine and creatine in Friedreich's ataxia. A randomized, placebo-controlled crossover trial von Schöls, L, Zange, J, Abele, M, Schillings, M, Skipka, G, Kuntz-Hehner, S, van Beekvelt, M C P, Colier, W N J M, Müller, K, Klockgether, T, Przuntek, H, Vorgerd, M

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Saccade Velocity as a Surrogate Disease Marker in Spinocerebellar Ataxia Type 2 von SEIFRIED, C, VELÁZQUEZ-PÉREZ, L, SANTOS-FALCÓN, N, ABELE, M, ZIEMANN, U, ALMAGUER, L E, MARTÍNEZ-GÓNGORA, E, SÁNCHEZ-CRUZ, G, CANALES, N, PÉREZ-GONZÁLEZ, R, VELÁZQUEZ-MANRESA, M, VIEBAHN, B, STUCKRAD-BARRE, S, KLOCKGETHER, T, FETTER, M., AUBURGER, G

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