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

Volltext

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.

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Cognitive deficits in spinocerebellar ataxia 2 von Bürk, K., Globas, C., Bösch, S., Gräber, S., Abele, M., Brice, A., Dichgans, J., Daum, I., Klockgether, T.

Volltext