Riess O - Search Results

1

SCA2 trinucleotide expansion in German SCA patients.

Riess O, Laccone FA, Gispert S, Schöls L, Zühlke C, Vieira-Saecker AM, Herlt S, Wessel K, Epplen JT, Weber BH, Kreuz F, Chahrokh-Zadeh S, Meindl A, Lunkes A, Aguiar J, Macek M Jr, Krebsová A, Macek M Sr, Bürk K, Tinschert S, Schreyer I, Pulst SM, Auburger G. Riess O, et al. Neurogenetics. 1997 May;1(1):59-64. doi: 10.1007/s100480050009. Neurogenetics. 1997. PMID: 10735276

2

Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients.

Schöls L, Vieira-Saecker AM, Schöls S, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Among authors: riess o. Hum Mol Genet. 1995 Jun;4(6):1001-5. doi: 10.1093/hmg/4.6.1001. Hum Mol Genet. 1995. PMID: 7655453

3

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.

Riess O, Schöls L, Bottger H, Nolte D, Vieira-Saecker AM, Schimming C, Kreuz F, Macek M Jr, Krebsová A, Macek M Sen, Klockgether T, Zühlke C, Laccone FA. Riess O, et al. Hum Mol Genet. 1997 Aug;6(8):1289-93. doi: 10.1093/hmg/6.8.1289. Hum Mol Genet. 1997. PMID: 9259275

4

Predominant neuronal expression of the gene responsible for dentatorubral-pallidoluysian atrophy (DRPLA) in rat.

Schmitt I, Epplen JT, Riess O. Schmitt I, et al. Among authors: riess o. Hum Mol Genet. 1995 Sep;4(9):1619-24. doi: 10.1093/hmg/4.9.1619. Hum Mol Genet. 1995. PMID: 8541849

5

Spinocerebellar ataxia type 1: Clinical and neurophysiological characteristics in German kindreds.

Schöls L, Riess O, Schöls S, Zeck S, Amoiridis G, Langkafel M, Epplen JT, Przuntek H. Schöls L, et al. Among authors: riess o. Acta Neurol Scand. 1995 Dec;92(6):478-85. doi: 10.1111/j.1600-0404.1995.tb00484.x. Acta Neurol Scand. 1995. PMID: 8750114

6

cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 gene.

Gossen M, Schmitt I, Obst K, Wahle P, Epplen JT, Riess O. Gossen M, et al. Among authors: riess o. Hum Mol Genet. 1996 Mar;5(3):381-9. doi: 10.1093/hmg/5.3.381. Hum Mol Genet. 1996. PMID: 8852664

7

Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

Schöls L, Amoiridis G, Epplen JT, Langkafel M, Przuntek H, Riess O. Schöls L, et al. Among authors: riess o. J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):466-70. doi: 10.1136/jnnp.61.5.466. J Neurol Neurosurg Psychiatry. 1996. PMID: 8937340 Free PMC article.

8

Transmission distortion of the mutant alleles in spinocerebellar ataxia.

Riess O, Epplen JT, Amoiridis G, Przuntek H, Schöls L. Riess O, et al. Hum Genet. 1997 Feb;99(2):282-4. doi: 10.1007/s004390050355. Hum Genet. 1997. PMID: 9048937

9

[Genetic diagnosis, classification and clinical hereditary ataxia disease entities].

Schöls L, Riess O, Amoiridis G, Riess A, Przuntek H, Epplen JT. Schöls L, et al. Among authors: riess o, riess a. Fortschr Neurol Psychiatr. 1997 Feb;65(2):79-89. doi: 10.1055/s-2007-996312. Fortschr Neurol Psychiatr. 1997. PMID: 9157050 Review. German.

10

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.

Schöls L, Gispert S, Vorgerd M, Menezes Vieira-Saecker AM, Blanke P, Auburger G, Amoiridis G, Meves S, Epplen JT, Przuntek H, Pulst SM, Riess O. Schöls L, et al. Among authors: riess o. Arch Neurol. 1997 Sep;54(9):1073-80. doi: 10.1001/archneur.1997.00550210011007. Arch Neurol. 1997. PMID: 9311350

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