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Page 1
IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations.
Weber F, Fontaine B, Cournu-Rebeix I, Kroner A, Knop M, Lutz S, Müller-Sarnowski F, Uhr M, Bettecken T, Kohli M, Ripke S, Ising M, Rieckmann P, Brassat D, Semana G, Babron MC, Mrejen S, Gout C, Lyon-Caen O, Yaouanq J, Edan G, Clanet M, Holsboer F, Clerget-Darpoux F, Müller-Myhsok B. Weber F, et al. Genes Immun. 2008 Apr;9(3):259-63. doi: 10.1038/gene.2008.14. Epub 2008 Mar 20. Genes Immun. 2008. PMID: 18354419
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.
Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Müller-Sarnowski F, Pfister H, Roeske D, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Müller-Myhsok B, Weber F. Nischwitz S, et al. J Neuroimmunol. 2010 Oct 8;227(1-2):162-6. doi: 10.1016/j.jneuroim.2010.06.003. Epub 2010 Jul 2. J Neuroimmunol. 2010. PMID: 20598377
More CLEC16A gene variants associated with multiple sclerosis.
Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Müller-Sarnowski F, Pfister H, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Müller-Myhsok B, Weber F. Nischwitz S, et al. Acta Neurol Scand. 2011 Jun;123(6):400-6. doi: 10.1111/j.1600-0404.2010.01421.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849399
Motor speech disorders in the nonfluent, semantic and logopenic variants of primary progressive aphasia.
Staiger A, Schroeter ML, Ziegler W, Schölderle T, Anderl-Straub S, Danek A, Duning T, Fassbender K, Fliessbach K, Jahn H, Kasper E, Kornhuber J, Landwehrmeyer B, Lauer M, Lombardi J, Ludolph A, Müller-Sarnowski F, Polyakova M, Prix C, Prudlo J, Regenbrecht F, Roßmeier C, Schneider A, Wiltfang J, Otto M; German FTLD Consortium; Diehl-Schmid J. Staiger A, et al. Among authors: muller sarnowski f. Cortex. 2021 Jul;140:66-79. doi: 10.1016/j.cortex.2021.03.017. Epub 2021 Apr 2. Cortex. 2021. PMID: 33933931
Therapeutic Drug Monitoring of Rivastigmine and Donepezil Under Consideration of CYP2D6 Genotype-Dependent Metabolism of Donepezil.
Ortner M, Stange M, Schneider H, Schröder C, Buerger K, Müller C, Müller-Sarnowski F, Diehl-Schmid J, Förstl H, Grimmer T, Steimer W. Ortner M, et al. Among authors: muller sarnowski f. Drug Des Devel Ther. 2020 Aug 11;14:3251-3262. doi: 10.2147/DDDT.S247259. eCollection 2020. Drug Des Devel Ther. 2020. PMID: 32848364 Free PMC article.
Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease.
Roeber S, Müller-Sarnowski F, Kress J, Edbauer D, Kuhlmann T, Tüttelmann F, Schindler C, Winter P, Arzberger T, Müller U, Danek A, Kretzschmar HA. Roeber S, et al. Among authors: muller sarnowski f. J Neural Transm (Vienna). 2015 Dec;122(12):1715-9. doi: 10.1007/s00702-015-1450-0. Epub 2015 Sep 8. J Neural Transm (Vienna). 2015. PMID: 26350633
Factors associated with the onset and persistence of post-lumbar puncture headache.
Monserrate AE, Ryman DC, Ma S, Xiong C, Noble JM, Ringman JM, Morris JC, Danek A, Müller-Sarnowski F, Clifford DB, McDade EM, Brooks WS, Darby DG, Masters CL, Weston PS, Farlow MR, Graff-Radford NR, Salloway SP, Fagan AM, Oliver A, Bateman RJ; Dominantly Inherited Alzheimer Network. Monserrate AE, et al. Among authors: muller sarnowski f. JAMA Neurol. 2015 Mar;72(3):325-32. doi: 10.1001/jamaneurol.2014.3974. JAMA Neurol. 2015. PMID: 25622095 Free PMC article.
14 results