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Absence of SCA1 mutation in idiopathic cerebellar ataxia.
Klockgether T, Bürk K, Schulz JB, Dichgans J, Wessel K, Auburger G. Klockgether T, et al. Among authors: burk k. J Neurol Neurosurg Psychiatry. 1994 Nov;57(11):1439-40. doi: 10.1136/jnnp.57.11.1439-a. J Neurol Neurosurg Psychiatry. 1994. PMID: 7964835 Free PMC article. No abstract available.
The natural history of degenerative ataxia: a retrospective study in 466 patients.
Klockgether T, Lüdtke R, Kramer B, Abele M, Bürk K, Schöls L, Riess O, Laccone F, Boesch S, Lopes-Cendes I, Brice A, Inzelberg R, Zilber N, Dichgans J. Klockgether T, et al. Among authors: burk k. Brain. 1998 Apr;121 ( Pt 4):589-600. doi: 10.1093/brain/121.4.589. Brain. 1998. PMID: 9577387
Risk factors for idiopathic cerebellar ataxia of late onset.
Klockgether T, Bürk K, Wüllner U, Wenning G, Schulz JB, Döller G, Wessel K, Huss P, Krämer A, Lüdtke R. Klockgether T, et al. Among authors: burk k. J Neurol Sci. 1998 Oct 8;160(2):171-4. doi: 10.1016/s0022-510x(98)00247-0. J Neurol Sci. 1998. PMID: 9849801
Evoked potentials in multiple system atrophy (MSA).
Abele M, Schulz JB, Bürk K, Topka H, Dichgans J, Klockgether T. Abele M, et al. Among authors: burk k. Acta Neurol Scand. 2000 Feb;101(2):111-5. doi: 10.1034/j.1600-0404.2000.101002111.x. Acta Neurol Scand. 2000. PMID: 10685858
Nerve conduction studies in multiple system atrophy.
Abele M, Schulz JB, Bürk K, Topka H, Dichgans J, Klockgether T. Abele M, et al. Among authors: burk k. Eur Neurol. 2000;43(4):221-3. doi: 10.1159/000008179. Eur Neurol. 2000. PMID: 10828652
236 results