Klockgether T - Search Results

1

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study.

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, Panzeri M, 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, Kang JS, Pandolfo M, Schulz JB, Molho S, Diallo A, Klockgether T. Jacobi H, et al. Among authors: klockgether t. Lancet Neurol. 2015 Nov;14(11):1101-8. doi: 10.1016/S1474-4422(15)00202-1. Epub 2015 Sep 13. Lancet Neurol. 2015. PMID: 26377379

2

The development of infratentorial atrophy in patients with idiopathic cerebellar ataxia of late onset: a CT study.

Klockgether T, Faiss J, Poremba M, Dichgans J. Klockgether T, et al. J Neurol. 1990 Nov;237(7):420-3. doi: 10.1007/BF00314733. J Neurol. 1990. PMID: 2273411

3

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.

4

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

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

Repeat length and disease progression in spinocerebellar ataxia type 3.

Klockgether T, Kramer B, Lüdtke R, Schöls L, Laccone F. Klockgether T, et al. Lancet. 1996 Sep 21;348(9030):830. doi: 10.1016/S0140-6736(05)65255-5. Lancet. 1996. PMID: 8814012 No abstract available.

9

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

10

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

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