Kết quả tìm kiếm - Mauri Reunanen
- Đang hiển thị 1 - 8 kết quả của 8
-
1
-
2
DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis Bằng Pirjo Isohanni, Tarja Linnankivi, Jana Buzková, Tuula Lönnqvist, Helena Pihko, Leena Valanne, Pentti J. Tienari, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Keijo Koivisto, Sanna Marjavaara, Anu Suomalainen
Được phát hành 2009Artigo -
3
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations Bằng Guðrún Kristjánsdóttir, Johanna K. Sandling, Alessandro Bonetti, Izaura M. Roos, Lili Milani, Chao Wang, Sigrun Gustafsdottir, Snævar Sigurðsson, Anders Lundmark, Pentti J. Tienari, Keijo Koivisto, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, L. Peltonen, Janna Saarela, Jan Hillert, Tomas Olsson, Ulf Landegren, Antonio Alcina, Óscar Fernández, Laura Leyva, María del Mar López-Guerrero, Miguel Lucas, Guillermo Izquierdo, Fuencisla Matesanz, A-C Syvänen
Được phát hành 2008Artigo -
4
Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene Bằng Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, Teppo Varilo, S. Kallio, Anu Kemppinen, Shaun Purcell, Keijo Koivisto, Pentti J. Tienari, Marja‐Liisa Sumelahti, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Arpo Aromaa, Annette Oturai, Helle Bach Søndergaard, Hanne F. Harbo, Inger‐Lise Mero, Stacey B. Gabriel, Daniel B. Mirel, Stephen L. Hauser, Ludwig Kappos, Chris H. Polman, Philip L. De Jager, David A. Hafler, Mark J. Daly, Aarno Palotie, Janna Saarela, Leena Peltonen
Được phát hành 2010Artigo -
5
Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls Bằng Sergio E. Baranzini, Pouya Khankhanian, Nikolaos A. Patsopoulos, Michael Li, Jim Stankovich, Chris Cotsapas, Helle Bach Søndergaard, Maria Ban, Nadia Barizzone, Laura Bergamaschi, David R. Booth, Dorothea Buck, Paola Cavalla, Elisabeth Gulowsen Celius, Manuel Comabella, Gıancarlo Comı, Alastair Compston, Isabelle Cournu‐Rebeix, Sandra D’Alfonso, Vincent Damotte, Lennox Din, Bénédicte Dubois, Irina Elovaara, Federica Esposito, Bertrand Fontaine, André Franke, An Goris, Pierre‐Antoine Gourraud, Christiane Graetz, Franca Rosa Guerini, Léna Guillot‐Noël, D Hafler, Hákon Hákonarson, Per Hall, Anders Hamsten, Hanne F. Harbo, Bernhard Hemmer, Jan Hillert, Anu Kemppinen, Ingrid Kockum, Keijo Koivisto, Malin Larsson, Mark Lathrop, Maurizio Leone, Christina M. Lill, Fabìo Macciardi, Roland Martinꝉ, Vittorio Martinelli, Filippo Martinelli Boneschi, Jacob L. McCauley, Kjell‐Morten Myhr, Paola Naldi, Tomas Olsson, Annette Oturai, Margaret A. Pericak‐Vance, Franco Perla, Mauri Reunanen, Janna Saarela, Safa Saker-Delye, Marco Salvetti, Finn Sellebjerg, Per Soelberg Sørensen, Anne Spurkland, Graeme J. Stewart, Bruce Taylor, Pentti J. Tienari, Juliane Winkelmann, Frauke Zipp, Adrian J. Ivinson, Jonathan L. Haines, Stephen Sawcer, Philip L. DeJager, Stephen L. Hauser, Jorge R. Oksenberg
Được phát hành 2013Revisão -
6
IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci Bằng Federica Esposito, Nikolaos A. Patsopoulos, Sabine Cepok, Ingrid Kockum, Virpi Leppä, David R. Booth, Robert Heard, Graeme J. Stewart, Mathew Cox, Rodney J. Scott, Jeannette Lechner‐Scott, An Goris, Rita Dobosi, Bénédicte Dubois, John D. Rioux, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Per Soelberg Sørensen, Mauri Reunanen, Keijo Koivisto, Isabelle Cournu‐Rebeix, B. Fontaine, Juliane Winkelmann, Christian Gieger, Carmen Infante‐Duarte, Frauke Zipp, Laura Bergamaschi, Maurizio Leone, Roberto Bergamaschi, Paola Cavalla, Åslaug Rudjord Lorentzen, I.-L. Mero, Elisabeth Gulowsen Celius, Hanne F. Harbo, Anne Spurkland, Manuel Comabella, B. Bryneda, Lars Alfredsson, Luisa Bernardinelli, Neil P. Robertson, Clive Hawkins, Lisa F. Barcellos, Gary W. Beecham, William S. Bush, Bruce Cree, Mark J. Daly, Adrian J. Ivinson, Cristin Aubin, Alastair Compston, Sandra D’Alfonso, J.L. Haines, Stephen L. Hauser, Bernhard Hemmer, Jan Hillert, Jacob L. McCauley, J. Oksenberg, Tomas Olsson, Aarno Palotie, L. Peltonen, Margaret A. Pericak‐Vance, Janna Saarela, Stephen Sawcer, Barbara E. Stranger, Filippo Martinelli Boneschi, Giancarlo Comi, D A Hafler, Paul I. W. de Bakker, Philip L. De Jager
Được phát hành 2010Revisão -
7
The 11-year long-term follow-up study from the randomized BENEFIT CIS trial Bằng Ludwig Kappos, Gilles Edan, Mark S. Freedman, Xavier Montalbán, Hans‐Peter Hartung, Bernhard Hemmer, Edward Fox, Frederik Barkhof, Sven Schippling, Andrea Schulze, Dirk Pleimes, Christoph Pohl, Rupert Sandbrink, Gustavo Cruz, Eva‐Maria Wicklein, Siegrid Strasser‐Fuchs, Thomas Berger, K. Vass, Christian Sindic, Bénédicte Dubois, Dominique Dive, Valérie Delvaux, Jason P. DeBruyne, Luanne M. Metz, G Rice, Marcelo Kremenchutzky, Pierre Duquette, Yves Lapierre, Mark Freedman, Anthony Traboulsee, Paul O’Connor, Pavel Štourač, Radomír Taláb, Martin Vališ, Olga Zapletalová, Ivana Kovářová, Eva Medová, Jiří Fiedler, Jette Lautrup Frederiksen, Bruno Brochet, T. Moreau, Patrick Vermersch, Jean Pelletier, Gilles Edan, Michel Clanet, David Brassat, Pierre Clavelou, Christine Lebrun‐Frénay, Olivier Gout, Mikko Kallela, Tuula Pirttilä, Juhani Ruutiainen, J-P Erälinna, Keijo Koivisto, Mauri Reunanen, I Keskinarkus, Irina Elovaara, Arno Villringer, H. Altenkirch, Lars Bauer, Mahdiyeh Khabbaz Koche Ghazi, Christoph Pohl, K. Wessel, HP Hartung, Wolfgang Steinke, B. C. Kieseier, Hans Wolfgang Kölmel, Patrick Oschmann, Martin Berghoff, Ricarda Diem, B. Kitze, Alexander Dressel, Francine Hoffmann, K. Baum, Simon Jung, H.-F. Petereit, D. Reske, Michael Sailer, Jürgen Köhler, Björn Tackenberg, Luisa Klotz, Reinhard Hohlfeld, Tania Kuempfel, K.T. Henn, Andreas Steinbrecher, Klemens Angstwurm, Hayrettin Tumani, Ralf Gold, Peter Rieckmann, Christoph Kleinschnitz, R Komoly, G Gács, Gábor Jakab, Gyula Pánczél, Tünde Csépány, László Csiba, László Vécsei, Ariel Miller, Dimitrios Karussis, Joab Chapman
Được phát hành 2016Artigo -
8
Long-term safety and efficacy of teriflunomide Bằng Paul O’Connor, Cristoforo Comi, Mark S. Freedman, Aaron Miller, Ludwig Kappos, Jean‐Pierre Bouchard, Christine Lebrun‐Frénay, Jan Mareš, Myriam Bénamor, Karthinathan Thangavelu, Jinjun Liang, Philippe Truffinet, Victoria Lawson, Jerry S. Wolinsky, E. Maida, Eduard Auff, Franz Fazekas, Thomas Berger, Virender Bhan, J-P Bouchard, Pierre Duquette, Mark S. Freedman, François Grand’Maison, M. Kremenchutzky, Caitlin Bourque, Ruth Ann Marrie, Maria Melanson, D. Patry, Paul O’Connor, Joël Oger, Mark Stefanelli, François Jacques, Pablo Venegas, Manoel Miranda, N. Barrientos, E Tenhamm, Sergio Gloger, Gernot Rohde, Jan Mareš, Jette Lautrup Frederiksen, Egon Stenager, Sulev Haldre, Katrin Gross‐Paju, Irina Elovaara, M-L Sumelahti, J-P Erälinna, J-P Erälinna, Martti Färkkilâ, Hanna Harno, Mauri Reunanen, T. Jolma, Cyrille B. Confavreux, William Camu, Pierre Clavelou, Laurent Magy, Marc Debouverie, Gilles Edan, Christine Lebrun‐Frénay, T. Moreau, Jean Pelletier, E Roullet, Sonia Alamowitch, M. Clanet, Patrick Hautecœur, Philippe Damier, L. Rumbach, Andrew Chan, Sebastian Schimrigk, J. Haas, Eckart Lensch, Hans‐Christoph Diener, Volker Limmroth, D. Anders, Martin Berghoff, Patrick Oschmann, Martin Stangel, Martin Berghoff, Achim Frese, Reinhard Kiefer, Martin Marziniak, Uwe K. Zettl, E. Stark, K. Jendroska, Gerd Reifschneider, Mauro Amato, Giacomo P. Comi, V. Cosi, Pamela Gallo, Claudio Gasperini, Angelo Ghezzi, María Trojano, Carlo Pozzilli, E. Montanari, Cees Zwanikken, P.J.H. Jongen, E.Th.L. van Munster, Raymond Hupperts, Bert W.M. Anten, E.A.C.M. Sanders, E. Celius
Được phát hành 2016Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Medicine
Multiple sclerosis
Biology
Gene
Genetics
Genotype
Immunology
Internal medicine
Single-nucleotide polymorphism
Allele
Genome-wide association study
Haplotype
Pathology
Alternative medicine
Expanded Disability Status Scale
Locus (genetics)
Placebo
Psychiatry
SNP
Adverse effect
Allele frequency
Antigen
Ataxia
Case-control study
Cerebrospinal fluid
Clinically isolated syndrome
Compound heterozygosity
Computational biology
Computer science
Environmental health