Résultats de la recherche - Hubert Kwieciński
- Résultat(s) 1 - 4 résultats de 4
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1
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia par GDJ Watts, Dana Thomasová, SK Ramdeen, Erin Fulchiero, SG Mehta, DA Drachman, C. Weihl, Zygmunt Jamrozik, Hubert Kwieciński, Anna Kamińska, VE Kimonis
Publié 2007Artigo -
2
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) par Martin Tristani‐Firouzi, Judy L. Jensen, Matthew R. Donaldson, Valeria Sansone, G. Meola, Angelika Hahn, Saı̈d Bendahhou, Hubert Kwieciński, Anna Fidziańska, Nikki Plaster, Ying‐Hui Fu, Louis J. Ptáček, Rabi Tawil
Publié 2002Artigo -
3
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway par Hsien-Yang Lee, Ying Xu, Yong Huang, Andrew H. Ahn, Georg Auburger, Massimo Pandolfo, Hubert Kwieciński, David A. Grimes, Anthony E. Lang, Jørgen E. Nielsen, Yuri Averyanov, Serenella Servidei, Andrzej Friedman, Patrick Van Bogaert, Marc Abramowicz, Michiko Kimura Bruno, Beatrice F. Sorensen, Ling Tang, Ying‐Hui Fu, Louis J. Ptáček
Publié 2004Artigo -
4
Characterizing absolute lymphocyte count profiles in dimethyl fumarate–treated patients with MS par Robert J. Fox, Andrew Chan, Ralf Gold, J. Theodore Phillips, Krzysztof Selmaj, Ih Chang, Mark Novas, Jitesh Rana, Jing L. Marantz, Zdeněk Ambler, Edvard Ehler, Eva Havrdová, Eva Meluzínová, Ivan Rektor, Radomír Taláb, Ralf Gold, Hans‐Peter Hartung, Attila Csányi, László Csiba, Gábor Jakab, Rogier Q. Hintzen, Chris H. Polman, Wiesław Drozdowski, Waldemar Fryze, Jan Kochanowicz, Hubert Kwieciński, Zdzislaw Maciejek, Sebastian Schimrigk, Krzysztof Selmaj, Andrzej Szczudlik, A Wajgt, Anna Belova, A. Boiko, Alexander Elchaninov, Kozlov Va, Odinak Mm, С Б Шварков, A A Skoromets, I D Stolyarov, O. V. Vorobieva, И. А. Завалишин, Jan Hillert, Tomas Olsson, Ludwig Kappos, Mefküre Eraksoy, Rana Karabudak, Aksel Sıva, Gavin Giovannoni, Clive Hawkins, Mohammed Sharief, Basil Sharrack, Christian Confavreux, John E. Ware, Michael Barnett, Mark Paine, Jeannette Lechner‐Scott, Roy G. Beran, Caron Chapman, Raymond Schwartz, Helmut Butzkueven, Reynolds F Casse, Richard Macdonell, Thomas Berger, Franz Fazekas, Gerhard Ransmayr, K. Vass, Shibeshih Belachew, Peter Paul De Deyn, D. Decoo, Bénédicte Dubois, Robert Medaer, Pierrette Seeldrayers, Christian Sindic, Luc Vande Gaer, Ludo Vanopdenbosch, Sanja Grgić, Amit Bar‐Or, Virender Bhan, Jean‐Pierre Bouchard, Suzanne Christie, Pierre Grammond, François Jacques, Felix Veloso, Galina Vorobeychik, Vesna Brinar, Vida Demarin, Josip Rudež, Silva Soldo-Butković, Ranka Baraba Vurdelja, Zdeněk Ambler, David Doležil, Eva Havrdová, Petr Kaňovský, Eva Meluzínová, Jiří Nova'k, Ivan Rektor, Ondřej Škoda, Marta Vachová Duchcovská, William Camu, Pierre Clavelou Antoanela
Publié 2016Artigo
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Medicine
Biology
Gene
Genetics
Internal medicine
Disease
Mutation
Afterdepolarization
Atrial fibrillation
Biochemistry
Biopsy
Cardiac arrhythmia
Cardiology
Channelopathy
Dementia
Dimethyl fumarate
Discontinuation
Dyskinesia
Electrophysiology
Endocrinology
Frontotemporal dementia
Gastroenterology
Gene expression
Gene isoform
Gene product
Immunology
Long QT syndrome
Lymphocyte
Missense mutation
Multiple sclerosis