Schöls L - Search Results

1

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.

Schmitz-Hübsch T, Coudert M, Bauer P, Giunti P, Globas C, Baliko L, Filla A, Mariotti C, Rakowicz M, Charles P, Ribai P, Szymanski S, Infante J, van de Warrenburg BP, Dürr A, Timmann D, Boesch S, Fancellu R, Rola R, Depondt C, Schöls L, Zdienicka E, Kang JS, Döhlinger S, Kremer B, Stephenson DA, Melegh B, Pandolfo M, di Donato S, du Montcel ST, Klockgether T. Schmitz-Hübsch T, et al. Among authors: schols l. Neurology. 2008 Sep 23;71(13):982-9. doi: 10.1212/01.wnl.0000325057.33666.72. Epub 2008 Aug 6. Neurology. 2008. PMID: 18685131 Free article.

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: schols s. Hum Mol Genet. 1995 Jun;4(6):1001-5. doi: 10.1093/hmg/4.6.1001. Hum Mol Genet. 1995. PMID: 7655453

3

Repeat length and disease progression in spinocerebellar ataxia type 3.

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

4

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. 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.

5

Transmission distortion of the mutant alleles in spinocerebellar ataxia.

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

6

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. Arch Neurol. 1997 Sep;54(9):1073-80. doi: 10.1001/archneur.1997.00550210011007. Arch Neurol. 1997. PMID: 9311350

7

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

Schöls L, Amoiridis G, Büttner T, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Ann Neurol. 1997 Dec;42(6):924-32. doi: 10.1002/ana.410420615. Ann Neurol. 1997. PMID: 9403486

8

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.

Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O. Schöls L, et al. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):67-73. doi: 10.1136/jnnp.64.1.67. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436730 Free PMC article.

9

Friedreich's ataxia. Revision of the phenotype according to molecular genetics.

Schöls L, Amoiridis G, Przuntek H, Frank G, Epplen JT, Epplen C. Schöls L, et al. Brain. 1997 Dec;120 ( Pt 12):2131-40. doi: 10.1093/brain/120.12.2131. Brain. 1997. PMID: 9448568

10

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

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