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2021

Development of SARA(home), a new video-based tool for the assessment of ataxia at home.
Grobe-Einsler, M. ORCID logoORCID: https://orcid.org/0000-0002-1808-2134, Taheri Amin, A., Faber, J., Schaprian, T., Jacobi, H., Schmitz-Hübsch, T. ORCID logoORCID: https://orcid.org/0000-0003-4833-5937, Diallo, A., Tezenas du Montcel, S. and Klockgether, T.
Movement Disorders 36 (5): 1242-1246. May 2021

2020

Brain iron and metabolic abnormalities in C19orf12 mutation carriers: a 7.0 tesla MRI study in mitochondrial membrane protein-associated neurodegeneration.
Dusek, P. ORCID logoORCID: https://orcid.org/0000-0003-4877-9642, Mekle, R., Skowronska, M., Acosta-Cabronero, J., Huelnhagen, T. ORCID logoORCID: https://orcid.org/0000-0002-6755-2171, Robinson, S.D., Schubert, F., Deschauer, M., Els, A., Ittermann, B., Schottmann, G., Madai, V.I. ORCID logoORCID: https://orcid.org/0000-0002-8552-6954, Paul, F. ORCID logoORCID: https://orcid.org/0000-0002-6378-0070, Klopstock, T., Kmiec, T., Niendorf, T. ORCID logoORCID: https://orcid.org/0000-0001-7584-6527, Wuerfel, J. ORCID logoORCID: https://orcid.org/0000-0002-0034-8053 and Schneider, S.A.
Movement Disorders 35 (1): 142-150. January 2020

2018

Mitochondrial dysfunction and increased glycolysis in prodromal and early Parkinson's blood cells.
Smith, A.M., Depp, C., Ryan, B.J., Johnston, G.I., Alegre-Abarrategui, J., Evetts, S., Rolinski, M., Baig, F., Ruffmann, C., Simon, A.K. ORCID logoORCID: https://orcid.org/0000-0002-4077-7995, Hu, M.T.M. and Wade-Martins, R.
Movement Disorders 33 (10): 1580-1590. October 2018

2016

A movement disorder with dystonia and ataxia caused by a mutation in the HIBCH gene.
Schottmann, G., Sarpong, A., Lorenz, C. ORCID logoORCID: https://orcid.org/0000-0002-7762-8133, Weinhold, N., Gill, E., Teschner, L., Ferdinandusse, S., Wanders, R.J.A., Prigione, A. ORCID logoORCID: https://orcid.org/0000-0001-9457-1952 and Schuelke, M. ORCID logoORCID: https://orcid.org/0000-0003-2824-3891
Movement Disorders 31 (11): 1733-1739. November 2016

2014

Reply to: Photoreceptor layer thinning in Parkinsonian syndromes.
Brandt, A.U. ORCID logoORCID: https://orcid.org/0000-0002-9768-014X, Paul, F. ORCID logoORCID: https://orcid.org/0000-0002-6378-0070 and Saidha, S.
Movement Disorders 29 (9): 1222-1223. August 2014

Photoreceptor layer thinning in idiopathic Parkinson's disease.
Roth, N.M., Saidha, S., Zimmermann, H. ORCID logoORCID: https://orcid.org/0000-0002-0276-8051, Brandt, A.U. ORCID logoORCID: https://orcid.org/0000-0002-9768-014X, Isensee, J., Benkhellouf-Rutkowska, A., Dornauer, M., Kühn, A.A., Mueller, T., Calabresi, P.A. and Paul, F. ORCID logoORCID: https://orcid.org/0000-0002-6378-0070
Movement Disorders 29 (9): 1163-1170. August 2014

2010

Camptocormia and myopathy.
Deuschl, G., Margraf, N., Spuler, S. ORCID logoORCID: https://orcid.org/0000-0002-0155-1117, 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. ORCID logoORCID: https://orcid.org/0000-0002-0155-1117, Krug, H., Klein, C., Medialdea, I.C., Jakob, W., Ebersbach, G., Gruber, D., Hoffmann, K.T., Trottenberg, T. and Kupsch, A.
Movement Disorders 25 (5): 552-559. 15 April 2010

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