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Page 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. Among authors: pulst sm. Neurogenetics. 1997 May;1(1):59-64. doi: 10.1007/s100480050009. Neurogenetics. 1997. PMID: 10735276
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: pulst sm. Arch Neurol. 1997 Sep;54(9):1073-80. doi: 10.1001/archneur.1997.00550210011007. Arch Neurol. 1997. PMID: 9311350
Screening for mutations in synaptotagmin XI in Parkinson's disease.
Glass AS, Huynh DP, Franck T, Woitalla D, Müller T, Pulst SM, Berg D, Krüger R, Riess O. Glass AS, et al. Among authors: pulst sm. J Neural Transm Suppl. 2004;(68):21-8. doi: 10.1007/978-3-7091-0579-5_3. J Neural Transm Suppl. 2004. PMID: 15354386
Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Tezenas du Montcel S, Durr A, Bauer P, Figueroa KP, Ichikawa Y, Brussino A, Forlani S, Rakowicz M, Schöls L, Mariotti C, van de Warrenburg BP, Orsi L, Giunti P, Filla A, Szymanski S, Klockgether T, Berciano J, Pandolfo M, Boesch S, Melegh B, Timmann D, Mandich P, Camuzat A; Clinical Research Consortium for Spinocerebellar Ataxia (CRC-SCA); EUROSCA network; Goto J, Ashizawa T, Cazeneuve C, Tsuji S, Pulst SM, Brusco A, Riess O, Brice A, Stevanin G. Tezenas du Montcel S, et al. Among authors: pulst sm. Brain. 2014 Sep;137(Pt 9):2444-55. doi: 10.1093/brain/awu174. Epub 2014 Jun 26. Brain. 2014. PMID: 24972706 Free PMC article.
261 results