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Brain iron and metabolic abnormalities in C19orf12 mutation carriers: a 7.0 tesla MRI study in mitochondrial membrane protein-associated neurodegeneration.
Dusek, P. and Mekle, R. and Skowronska, M. and Acosta-Cabronero, J. and Huelnhagen, T. and Robinson, S.D. and Schubert, F. and Deschauer, M. and Els, A. and Ittermann, B. and Schottmann, G. and Madai, V.I. and Paul, F. and Klopstock, T. and Kmiec, T. and Niendorf, T. and Wuerfel, J. and Schneider, S.A.
Movement Disorders 35 (1): 142-150. January 2020


A movement disorder with dystonia and ataxia caused by a mutation in the HIBCH gene.
Schottmann, G. and Sarpong, A. and Lorenz, C. and Weinhold, N. and Gill, E. and Teschner, L. and Ferdinandusse, S. and Wanders, R.J.A. and Prigione, A. and Schuelke, M.
Movement Disorders 31 (11): 1733-1739. November 2016


Reply to: Photoreceptor layer thinning in Parkinsonian syndromes.
Brandt, A.U. and Paul, F. and Saidha, S.
Movement Disorders 29 (9): 1222-1223. August 2014

Photoreceptor layer thinning in idiopathic Parkinson's disease.
Roth, N.M. and Saidha, S. and Zimmermann, H. and Brandt, A.U. and Isensee, J. and Benkhellouf-Rutkowska, A. and Dornauer, M. and Kühn, A.A. and Mueller, T. and Calabresi, P.A. and Paul, F.
Movement Disorders 29 (9): 1163-1170. August 2014


Camptocormia and myopathy.
Deuschl, G. and Margraf, N. and Spuler, S. and Kupsch, A. and Schulz-Schaeffer, W.J.
Movement Disorders 25 (15): 2689-2690. 15 November 2010

Myopathy causing camptocormia in idiopathic Parkinson's disease: a multidisciplinary approach.
Spuler, S. and Krug, H. and Klein, C. and Medialdea, I.C. and Jakob, W. and Ebersbach, G. and Gruber, D. and Hoffmann, K.T. and Trottenberg, T. and Kupsch, A.
Movement Disorders 25 (5): 552-559. 15 April 2010

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