Bürk K - Search Results

1

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

2

[Classification and diagnosis of degenerative ataxias].

Klockgether T, Bürk K, Auburger G, Dichgans J. Klockgether T, et al. Among authors: burk k. Nervenarzt. 1995 Aug;66(8):571-81. Nervenarzt. 1995. PMID: 7566268 Review. German.

3

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.

4

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

5

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

6

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.

Stevanin G, Trottier Y, Cancel G, Dürr A, David G, Didierjean O, Bürk K, Imbert G, Saudou F, Abada-Bendib M, Gourfinkel-An I, Benomar A, Abbas N, Klockgether T, Grid D, Agid Y, Mandel JL, Brice A. Stevanin G, et al. Among authors: burk k. Hum Mol Genet. 1996 Dec;5(12):1887-92. doi: 10.1093/hmg/5.12.1887. Hum Mol Genet. 1996. PMID: 8968739

7

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

8

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.

Cancel G, Dürr A, Didierjean O, Imbert G, Bürk K, Lezin A, Belal S, Benomar A, Abada-Bendib M, Vial C, Guimarães J, Chneiweiss H, Stevanin G, Yvert G, Abbas N, Saudou F, Lebre AS, Yahyaoui M, Hentati F, Vernant JC, Klockgether T, Mandel JL, Agid Y, Brice A. Cancel G, et al. Among authors: burk k. Hum Mol Genet. 1997 May;6(5):709-15. doi: 10.1093/hmg/6.5.709. Hum Mol Genet. 1997. PMID: 9158145

9

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.

10

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

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