Klockgether T - Search Results

1

Second consensus statement on the diagnosis of multiple system atrophy.

Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, Trojanowski JQ, Wood NW, Colosimo C, Dürr A, Fowler CJ, Kaufmann H, Klockgether T, Lees A, Poewe W, Quinn N, Revesz T, Robertson D, Sandroni P, Seppi K, Vidailhet M. Gilman S, et al. Among authors: klockgether t. Neurology. 2008 Aug 26;71(9):670-6. doi: 10.1212/01.wnl.0000324625.00404.15. Neurology. 2008. PMID: 18725592 Free PMC article.

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

Magnetic resonance imaging in hereditary and idiopathic ataxia.

Wüllner U, Klockgether T, Petersen D, Naegele T, Dichgans J. Wüllner U, et al. Among authors: klockgether t. Neurology. 1993 Feb;43(2):318-25. doi: 10.1212/wnl.43.2.318. Neurology. 1993. PMID: 8437696

4

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

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

6

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

7

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. Among authors: klockgether t. 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.

8

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. Brain. 1998 Apr;121 ( Pt 4):589-600. doi: 10.1093/brain/121.4.589. Brain. 1998. PMID: 9577387

9

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

10

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. J Neurol Sci. 1998 Oct 8;160(2):171-4. doi: 10.1016/s0022-510x(98)00247-0. J Neurol Sci. 1998. PMID: 9849801

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