Klockgether T - Search Results

1

Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3.

Faber J, Schaprian T, Berkan K, Reetz K, França MC Jr, de Rezende TJR, Hong J, Liao W, van de Warrenburg B, van Gaalen J, Durr A, Mochel F, Giunti P, Garcia-Moreno H, Schoels L, Hengel H, Synofzik M, Bender B, Oz G, Joers J, de Vries JJ, Kang JS, Timmann-Braun D, Jacobi H, Infante J, Joules R, Romanzetti S, Diedrichsen J, Schmid M, Wolz R, Klockgether T. Faber J, et al. Among authors: klockgether t. Mov Disord. 2021 Oct;36(10):2273-2281. doi: 10.1002/mds.28610. Epub 2021 May 5. Mov Disord. 2021. PMID: 33951232 Free PMC article.

2

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: klockgether t. Hum Mol Genet. 1996 Dec;5(12):1887-92. doi: 10.1093/hmg/5.12.1887. Hum Mol Genet. 1996. PMID: 8968739

3

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: klockgether t. Hum Mol Genet. 1997 May;6(5):709-15. doi: 10.1093/hmg/6.5.709. Hum Mol Genet. 1997. PMID: 9158145

4

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. Brain. 1998 Sep;121 ( Pt 9):1687-93. doi: 10.1093/brain/121.9.1687. Brain. 1998. PMID: 9762957

5

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. 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.

6

The molecular biology of the autosomal-dominant cerebellar ataxias.

Klockgether T, Wüllner U, Spauschus A, Evert B. Klockgether T, et al. Mov Disord. 2000 Jul;15(4):604-12. doi: 10.1002/1531-8257(200007)15:4<604::aid-mds1004>3.0.co;2-k. Mov Disord. 2000. PMID: 10928570 Review.

7

Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3.

Abele M, Bürk K, Laccone F, Dichgans J, Klockgether T. Abele M, et al. Among authors: klockgether t. J Neurol. 2001 Apr;248(4):311-4. doi: 10.1007/s004150170206. J Neurol. 2001. PMID: 11374096

8

Executive dysfunction in spinocerebellar ataxia type 1.

Bürk K, Bösch S, Globas C, Zühlke C, Daum I, Klockgether T, Dichgans J. Bürk K, et al. Among authors: klockgether t. Eur Neurol. 2001;46(1):43-8. doi: 10.1159/000050755. Eur Neurol. 2001. PMID: 11455183

9

Inflammatory genes are upregulated in expanded ataxin-3-expressing cell lines and spinocerebellar ataxia type 3 brains.

Evert BO, Vogt IR, Kindermann C, Ozimek L, de Vos RA, Brunt ER, Schmitt I, Klockgether T, Wüllner U. Evert BO, et al. Among authors: klockgether t. J Neurosci. 2001 Aug 1;21(15):5389-96. doi: 10.1523/JNEUROSCI.21-15-05389.2001. J Neurosci. 2001. PMID: 11466410 Free PMC article.

10

State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.

Gasser T, Bressman S, Dürr A, Higgins J, Klockgether T, Myers RH. Gasser T, et al. Among authors: klockgether t. Mov Disord. 2003 Jan;18(1):3-18. doi: 10.1002/mds.10338. Mov Disord. 2003. PMID: 12518296 Review.

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