Riess O - Search Results

1

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.

Schüle R, Schlipf N, Synofzik M, Klebe S, Klimpe S, Hehr U, Winner B, Lindig T, Dotzer A, Riess O, Winkler J, Schöls L, Bauer P. Schüle R, et al. Among authors: riess o. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1402-4. doi: 10.1136/jnnp.2008.167528. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917823

2

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. Among authors: riess o. 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.

3

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.

4

Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?

Schöls L, Haan J, Riess O, Amoiridis G, Przuntek H. Schöls L, et al. Among authors: riess o. Neurology. 1998 Dec;51(6):1603-7. doi: 10.1212/wnl.51.6.1603. Neurology. 1998. PMID: 9855509

5

Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients.

Schlipf NA, Schüle R, Klimpe S, Karle KN, Synofzik M, Schicks J, Riess O, Schöls L, Bauer P. Schlipf NA, et al. Among authors: riess o. Clin Genet. 2011 Aug;80(2):148-60. doi: 10.1111/j.1399-0004.2011.01715.x. Epub 2011 Jun 13. Clin Genet. 2011. PMID: 21623769

6

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. Among authors: riess o. Ann Neurol. 1997 Dec;42(6):924-32. doi: 10.1002/ana.410420615. Ann Neurol. 1997. PMID: 9403486

7

Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD).

Klockgether T, Schöls L, Abele M, Bürk K, Topka H, Andres F, Amoiridis G, Lüdtke R, Riess O, Laccone F, Dichgans J. Klockgether T, et al. Among authors: riess o. J Neurol Neurosurg Psychiatry. 1999 Feb;66(2):222-4. doi: 10.1136/jnnp.66.2.222. J Neurol Neurosurg Psychiatry. 1999. PMID: 10071104 Free PMC article.

8

Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP).

Seidel K, De Vos R, Derksen L, Bauer P, Riess O, den Dunnen W, Deller T, Hageman G, Rüb U. Seidel K, et al. Among authors: riess o. Ann Anat. 2009 Apr;191(2):203-11. doi: 10.1016/j.aanat.2008.11.003. Epub 2009 Jan 20. Ann Anat. 2009. PMID: 19230631

9

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

10

Extrapyramidal motor signs in degenerative ataxias.

Schöls L, Peters S, Szymanski S, Krüger R, Lange S, Hardt C, Riess O, Przuntek H. Schöls L, et al. Among authors: riess o. Arch Neurol. 2000 Oct;57(10):1495-500. doi: 10.1001/archneur.57.10.1495. Arch Neurol. 2000. PMID: 11030803

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