Klockgether T - Search Results

1

Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias.

Jacobi H, du Montcel ST, Bauer P, Giunti P, Cook A, Labrum R, Parkinson MH, Durr A, Brice A, Charles P, Marelli C, Mariotti C, Nanetti L, Sarro L, Rakowicz M, Sulek A, Sobanska A, Schmitz-Hübsch T, Schöls L, Hengel H, Baliko L, Melegh B, Filla A, Antenora A, Infante J, Berciano J, van de Warrenburg BP, Timmann D, Szymanski S, Boesch S, Nachbauer W, Kang JS, Pandolfo M, Schulz JB, Melac AT, Diallo A, Klockgether T. Jacobi H, et al. Among authors: klockgether t. J Neurol. 2018 Sep;265(9):2040-2051. doi: 10.1007/s00415-018-8954-0. Epub 2018 Jun 29. J Neurol. 2018. PMID: 29959555

2

Multiple system atrophy: natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT.

Schulz JB, Klockgether T, Petersen D, Jauch M, Müller-Schauenburg W, Spieker S, Voigt K, Dichgans J. Schulz JB, et al. Among authors: klockgether t. J Neurol Neurosurg Psychiatry. 1994 Sep;57(9):1047-56. doi: 10.1136/jnnp.57.9.1047. J Neurol Neurosurg Psychiatry. 1994. PMID: 8089667 Free PMC article.

3

Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia.

Fetter M, Klockgether T, Schulz JB, Faiss J, Koenig E, Dichgans J. Fetter M, et al. Among authors: klockgether t. J Neurol. 1994 Feb;241(4):234-41. doi: 10.1007/BF00863774. J Neurol. 1994. PMID: 8195823

4

Clinical and imaging correlations in inherited ataxias.

Klockgether T, Wüllner U, Dichgans J, Grodd W, Nägele T, Petersen D, Schroth G, Schmidt O, Voigt K. Klockgether T, et al. Adv Neurol. 1993;61:77-96. Adv Neurol. 1993. PMID: 8421970 Review. No abstract available.

5

Fixation instability and oculomotor abnormalities in Friedreich's ataxia.

Spieker S, Schulz JB, Petersen D, Fetter M, Klockgether T, Dichgans J. Spieker S, et al. Among authors: klockgether t. J Neurol. 1995 Aug;242(8):517-21. doi: 10.1007/BF00867423. J Neurol. 1995. PMID: 8530980

6

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. Neurology. 1996 Jan;46(1):118-21. doi: 10.1212/wnl.46.1.118. Neurology. 1996. PMID: 8559357

7

Potassium deprivation-induced apoptosis of cerebellar granule neurons: a sequential requirement for new mRNA and protein synthesis, ICE-like protease activity, and reactive oxygen species.

Schulz JB, Weller M, Klockgether T. Schulz JB, et al. Among authors: klockgether t. J Neurosci. 1996 Aug 1;16(15):4696-706. doi: 10.1523/JNEUROSCI.16-15-04696.1996. J Neurosci. 1996. PMID: 8764657 Free PMC article.

8

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. Among authors: klockgether t. Brain. 1996 Oct;119 ( Pt 5):1497-505. doi: 10.1093/brain/119.5.1497. Brain. 1996. PMID: 8931575

9

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

10

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. Among authors: klockgether t. J Neurol. 1997 Apr;244(4):256-61. doi: 10.1007/s004150050081. J Neurol. 1997. PMID: 9112595

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