Burk K - Search Results

1

The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.

Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Pellecchia MT, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T; European Multiple System Atrophy Study Group. Kamm C, et al. Among authors: burk k. Brain. 2005 Aug;128(Pt 8):1855-60. doi: 10.1093/brain/awh535. Epub 2005 Jun 9. Brain. 2005. PMID: 15947063

2

Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imaging.

Klockgether T, Zühlke C, Schulz JB, Bürk K, Fetter M, Dittmann H, Skalej M, Dichgans J. Klockgether T, et al. Among authors: burk k. Neurology. 1996 Jan;46(1):118-21. doi: 10.1212/wnl.46.1.118. Neurology. 1996. PMID: 8559357

3

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

Bürk K, Abele M, Fetter M, Dichgans J, Skalej M, Laccone F, Didierjean O, Brice A, Klockgether T. Bürk K, et al. Brain. 1996 Oct;119 ( Pt 5):1497-505. doi: 10.1093/brain/119.5.1497. Brain. 1996. PMID: 8931575

4

Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.

Bürk K, Stevanin G, Didierjean O, Cancel G, Trottier Y, Skalej M, Abele M, Brice A, Dichgans J, Klockgether T. Bürk K, et al. J Neurol. 1997 Apr;244(4):256-61. doi: 10.1007/s004150050081. J Neurol. 1997. PMID: 9112595

5

Saccade velocity in idiopathic and autosomal dominant cerebellar ataxia.

Bürk K, Fetter M, Skalej M, Laccone F, Stevanin G, Dichgans J, Klockgether T. Bürk K, et al. J Neurol Neurosurg Psychiatry. 1997 Jun;62(6):662-4. doi: 10.1136/jnnp.62.6.662. J Neurol Neurosurg Psychiatry. 1997. PMID: 9219762 Free PMC article.

6

Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.

Abele M, Bürk K, Andres F, Topka H, Laccone F, Bösch S, Brice A, Cancel G, Dichgans J, Klockgether T. Abele M, et al. Among authors: burk k. Brain. 1997 Dec;120 ( Pt 12):2141-8. doi: 10.1093/brain/120.12.2141. Brain. 1997. PMID: 9448569

7

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

8

Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.

Klockgether T, Skalej M, Wedekind D, Luft AR, Welte D, Schulz JB, Abele M, Bürk K, Laccone F, Brice A, Dichgans J. Klockgether T, et al. Among authors: burk k. Brain. 1998 Sep;121 ( Pt 9):1687-93. doi: 10.1093/brain/121.9.1687. Brain. 1998. PMID: 9762957

9

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

10

Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD).

Klockgether T, Schöls L, Abele M, Bürk K, Topka H, Andres F, Amoiridis G, Lüdtke R, Riess O, Laccone F, Dichgans J. Klockgether T, et al. Among authors: burk k. J Neurol Neurosurg Psychiatry. 1999 Feb;66(2):222-4. doi: 10.1136/jnnp.66.2.222. J Neurol Neurosurg Psychiatry. 1999. PMID: 10071104 Free PMC article.

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