Stefan Waibel
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
van Rheenen W, de Visser M, Weber M, Robberecht W, Hardiman O, Shaw P, Shaw C, Morrison K, Al-Chalabi A, Andersen P, Ludolph A, Veldink J, van der Kooi A, Schelhaas H, Waibel S, Diekstra F, van Doormaal P, Seelen M, Kenna K, McLaughlin R, Shatunov A, Czell D, van Es M, van Vught P, Van Damme P, Smith B, van den Berg L. H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis. Neurobiol Aging 2012; 34:1517.e5-7.
11.10.2012H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
11.10.2012Neurobiol Aging 2012; 34:1517.e5-7
van Rheenen Wouter, de Visser Marianne, Weber Markus, Robberecht Wim, Hardiman Orla, Shaw Pamela J, Shaw Christopher E, Morrison Karen E, Al-Chalabi Ammar, Andersen Peter M, Ludolph Albert C, Veldink Jan H, van der Kooi Anneke J, Schelhaas H Jurgen, Waibel Stefan, Diekstra Frank P, van Doormaal Perry T C, Seelen Meinie, Kenna Kevin, McLaughlin Russell, Shatunov Aleksey, Czell David, van Es Michael A, van Vught Paul W J, Van Damme Philip, Smith Bradley N, van den Berg Leonard H
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
van den Berg L, Heutink P, van Hilten J, Verbaan D, de Visser M, van der Kooi A, Weber M, Klein C, Waibel S, Fernández-Santiago R, Birve A, Dahlberg C, Lemmens R, Hennekam E, Cuppen E, van de Warrenburg B, Landers J, de Bakker P, Pasterkamp R, Veldink J, Ophoff R, Robberecht W, Ludolph A, Gasser T, Silani V, Brown R, Berg D, Van Damme P, Pezzoli G, Keagle P, LeClerc A, Fumoto K, Diekstra F, Koppers M, Blauw H, Schulte C, Groen E, Andersen P, Ticozzi N, van Vught P, Schelhaas H, Bloem B, Scheffer H, Goldwurm S, Mariani C, Folkerth R, Wu D, Kishikawa H, Yu W, Hu G, Lowe P, Wills A, van Rheenen W, van Blitterswijk M, van Nuenen B, van Es M. Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Ann Neurol 2011; 70:964-73.
01.12.2011Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
01.12.2011Ann Neurol 2011; 70:964-73
van den Berg Leonard H, Heutink Peter, van Hilten Jacobus J, Verbaan Dagmar, de Visser Marianne, van der Kooi Anneke J, Weber Markus, Klein Christine, Waibel Stefan, Fernández-Santiago Rubén, Birve Anna, Dahlberg Caroline, Lemmens Robin, Hennekam Eric A M, Cuppen Edwin, van de Warrenburg Bart P, Landers John E, de Bakker Paul I W, Pasterkamp R Jeroen, Veldink Jan H, Ophoff Roel A, Robberecht Wim, Ludolph Albert C, Gasser Thomas, Silani Vincenzo, Brown Robert H, Berg Daniela, Van Damme Philip, Pezzoli Gianni, Keagle Pamela, LeClerc Ashley Lyn, Fumoto Katsumi, Diekstra Frank P, Koppers Max, Blauw Hylke M, Schulte Claudia, Groen Ewout J N, Andersen Peter M, Ticozzi Nicola, van Vught Paul W J, Schelhaas Helenius J, Bloem Bastiaan R, Scheffer Hans, Goldwurm Stefano, Mariani Claudio, Folkerth Rebecca D, Wu David, Kishikawa Hiroko, Yu Wenhao, Hu Guo-fu, Lowe Patrick P, Wills Anne-Marie, van Rheenen Wouter, van Blitterswijk Marka, van Nuenen Bart F L, van Es Michael A
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect
Gispert S, Ludolph A, Riess O, Krüger R, Andersen P, Berg D, Weber M, Becker T, Gitler A, Geisen C, Liepelt I, Bauer P, Waibel S, Kurz A, Auburger G. The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Neurobiol Dis 2011; 45:356-61.
25.08.2011The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect
25.08.2011Neurobiol Dis 2011; 45:356-61
Gispert Suzana, Ludolph Albert C, Riess Olaf, Krüger Rejko, Andersen Peter M, Berg Daniela, Weber Markus, Becker Tim, Gitler Aaron D, Geisen Christof, Liepelt Inga, Bauer Peter, Waibel Stefan, Kurz Alexander, Auburger Georg
The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families
Rabe M, Felbecker A, Waibel S, Steinbach P, Winter P, Müller U, Ludolph A. The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families. J Neurol 2010; 257:1298-302.
23.03.2010The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families
23.03.2010J Neurol 2010; 257:1298-302
Rabe Malessa, Felbecker Ansgar, Waibel Stefan, Steinbach Peter, Winter Pia, Müller Ulrich, Ludolph Albert C