Lernbereich: was ist das? Eine didaktische Aufgabe (nicht nur) für die Grundschule Enseignement pluridisciplinaire qu'est-ce que c'est? Une tâche didactique, (pas seulement) pour les écoles primairesBURK K.Westermanns Pädagogische Beiträge. 1977, Vol 29, Num 1, pp 28-34Article

Information resources management in the R&D environmentBÜRK, K.AGARD conference proceedings. 1986, Num 385, pp 10.1-10.4, issn 0549-7191Conference Paper

Perceptual and Acoustic Correlates of Aging in the Speech of MalesRYAN W. J; BURK K. W.Journal of Communication Disorders. 1974, Vol 7, Num 2, pp 181-192Article

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3BÜRK, K; GLOBAS, C; BÖSCH, S et al.Journal of neurology. 2003, Vol 250, Num 2, pp 207-211, issn 0340-5354, 5 p.Article

Executive dysfunction in spinocerebellar ataxia type 1BÜRK, K; BÖSCH, S; GLOBAS, C et al.European neurology. 2001, Vol 46, Num 1, pp 43-48, issn 0014-3022Article

Autosomal dominant cerebellar ataxia type I: Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3ABELE, M; BÜRK, K; ANDRES, F et al.Brain. 1997, Vol 120, pp 2141-2148, issn 0006-8950, 12Article

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasSTEVANIN, G; TROTTIER, Y; GOURFINKEL-AN, I et al.Human molecular genetics (Print). 1996, Vol 5, Num 12, pp 1887-1892, issn 0964-6906Article

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegiaBEETZ, C; NYGREN, A. O. H; OTTO, S et al.Neurology. 2006, Vol 67, Num 11, pp 1926-1930, issn 0028-3878, 5 p.Article

Sporadic cerebellar ataxia associated with gluten sensitivityBÜRK, K; BÖSCH, S; KLOCKGETHER, T et al.Brain. 2001, Vol 124, pp 1013-1019, issn 0006-8950, 5Article

Oxidative stress in patients with Friedreich ataxiaSCHULZ, J. B; DEHMER, T; BOGDANOV, M. B et al.Neurology. 2000, Vol 55, Num 11, pp 1719-1721, issn 0028-3878Article

The natural history of degenerative ataxia : a retrospective study in 466 patientsKLOCKGETHER, T; LÜDTKE, R; BRICE, A et al.Brain. 1998, Vol 121, pp 589-600, issn 0006-8950, 4Article

Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significanceRÜB, U; BRUNT, E. R; BRAAK, H et al.Neuropathology and applied neurobiology (Print). 2004, Vol 30, Num 4, pp 402-414, issn 0305-1846, 13 p.Article

Spinocerebellar ataxia type 5: Clinical and molecular genetic features of a German kindredBÜRK, K; ZÜHLKE, C; KÖNIG, I. R et al.Neurology. 2004, Vol 62, Num 2, pp 327-329, issn 0028-3878, 3 p.Article

Evoked potentials in multiple system atrophy (MSA)ABELE, M; SCHULZ, J. B; BÜRK, K et al.Acta neurologica scandinavica. 2000, Vol 101, Num 2, pp 111-115, issn 0001-6314Article

Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)KLOCKGETHER, T; SCHÖLS, L; DICHGANS, J et al.Journal of neurology, neurosurgery and psychiatry. 1999, Vol 66, Num 2, pp 222-224, issn 0022-3050Article

Autosomal dominant cerebellar ataxia type I : oculomotor abnormalities in families with SCA1, SCA2, and SCA3BÜRK, K; FETTER, M; ABELE, M et al.Journal of neurology. 1999, Vol 246, Num 9, pp 789-797, issn 0340-5354Article

Spinocerebellar ataxia type 6 : Evidence for a strong founder effect among German familiesDICHGANS, M; SCHÖLS, L; RIESS, O et al.Neurology. 1999, Vol 52, Num 4, pp 849-851, issn 0028-3878Article

Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insightsRÜB, U; BÜRK, K; SCHWARZACHER, S et al.Neuropathology and applied neurobiology (Print). 2012, Vol 38, Num 7, pp 665-680, issn 0305-1846, 16 p.Article

MRI-based volumetric differentiation of sporadic cerebellar ataxiaBÜRK, K; GLOBAS, C; WAHL, T et al.Brain. 2004, Vol 127, pp 175-181, issn 0006-8950, 7 p., 1Article

Linkage disequilibrium at the SCA2 locusDIDIERJEAN, O; CANCEL, G; BRICE, A et al.Journal of medical genetics. 1999, Vol 36, Num 5, pp 415-417, issn 0022-2593Article

A new semiautomated, three-dimensional technique allowing precise quantification of total and regional cerebellar volume using MRILUFT, A. R; SKALEJ, M; WELTE, D et al.Magnetic resonance in medicine. 1998, Vol 40, Num 1, pp 143-151, issn 0740-3194Article

Saccade velocity in idiopathic and autosomal dominant cerebellar ataxiaBÜRK, K; FETTER, M; SKALEJ, M et al.Journal of neurology, neurosurgery and psychiatry. 1997, Vol 62, Num 6, pp 662-664, issn 0022-3050Article

Friedreich's ataxia with retained tendon reflexes : molecular genetics, clinical neurophysiology, and magnetic resonance imagingKLOCKGETHER, T; ZÜHLKE, C; SCHULZ, J. B et al.Neurology. 1996, Vol 46, Num 1, pp 118-121, issn 0028-3878Article

Antineuronal antibodies in sporadic late-onset cerebellar ataxiaBÜRK, K; WICK, M; ROTH, G et al.Journal of neurology. 2010, Vol 257, Num 1, pp 59-62, issn 0340-5354, 4 p.Article

Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7)HOCHE, F; SEIDEL, K; VAN BROECKHOVEN, C et al.Neuropathology and applied neurobiology (Print). 2008, Vol 34, Num 5, pp 479-491, issn 0305-1846, 13 p.Article