Søgeresultater - Е. Л. Дадали

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  1. 1
    A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene

    A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene af Irina Mersiyanova, Alexander V. Perepelov, A. V. Polyakov, V. F. Sitnikov, Е. Л. Дадали, Roman B. Oparin, А. Н. Петрин, Oleg V. Evgrafov

    Udgivet 2000
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    Artigo
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  2. 2
    Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

    Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients af Irina Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Е. Л. Дадали, В. П. Федотов, Eva Nelis, Ann L�fgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov

    Udgivet 2000
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    Artigo
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  3. 3
    Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

    Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A af Stephan Züchner, Irina Mersiyanova, M. Muglia, Nisrine Bissar‐Tadmouri, Julie M. Rochelle, Е. Л. Дадали, Mario Zappia, Eva Nelis, A. Patitucci, Jan Senderek, Yeşim Parman, Oleg V. Evgrafov, Peter De Jonghe, Yuji Takahashi, Shoij Tsuji, Margaret A. Pericak‐Vance, Aldo Quattrone, Esra Battologlu, A. V. Polyakov, Vincent Timmerman, J. M. Schröder, Jeffery M. Vance

    Udgivet 2004
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    Artigo
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  4. 4
    Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

    Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy af Oleg V. Evgrafov, Irina Mersiyanova, Joy Irobi, Ludo Van Den Bosch, Ines Dierick, Conrad L. Leung, O. A. Schagina, Nathalie Verpoorten, Katrien Van Impe, В. П. Федотов, Е. Л. Дадали, Michaela Auer‐Grumbach, Christian Windpassinger, Klaus Wagner, Zoran D‎. Mitrović, David Hilton‐Jones, Kevin Talbot, Jean‐Jacques Martin, Natalia Vasserman, Svetlana Tverskaya, A. V. Polyakov, Ronald K.H. Liem, Jan Gettemans, Wim Robberecht, Peter De Jonghe, Vincent Timmerman

    Udgivet 2004
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    Artigo
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  5. 5
    Genotype-phenotype correlations in <i>SCN8A</i>-related disorders reveal prognostic and therapeutic implications

    Genotype-phenotype correlations in <i>SCN8A</i>-related disorders reveal prognostic and therapeutic implications af Katrine M. Johannesen, Yuanyuan Liu, Mahmoud Koko, Cathrine E. Gjerulfsen, Lukas Sonnenberg, Julian Schubert, Christina Fenger, Ahmed Eltokhi, Maert Rannap, Nils A. Koch, Stephan Lauxmann, Johanna Krüger, Josua Kegele, Laura Canafoglia, Silvana Franceschetti, Patrick May, Johannes Rebstock, Pia Zacher, Susanne Ruf, Michael Alber, Katalin Štěrbová, Petra Laššuthová, Markéta Vlčková, Johannes R. Lemke, Konrad Platzer, Ilona Krey, Constanze Heine, Dagmar Wieczorek, Judith Kroell-Seger, Caroline Lund, Karl Martin Klein, P Y Billie Au, Jong M. Rho, Alice Ho, Silvia Masnada, Pierangelo Veggiotti, Lucio Giordano, Patrizia Accorsi, Christina Engel Hoei‐Hansen, Pasquale Striano, Federico Zara, Hélène Verhelst, J. Verhoeven, Hilde M. H. Braakman, Bert van der Zwaag, Aster V. E. Harder, Eva H. Brilstra, Manuela Pendziwiat, Sebastian Lebon, María Vaccarezza, Ngọc Minh Lê, Jakob Christensen, Sabine Grønborg, Stephen W. Scherer, Jennifer Howe, Walid Fazeli, Katherine B. Howell, Richard J. Leventer, Chloe Stutterd, Sonja Walsh, Marion Gérard, Bénédicte Gérard, Sara Matricardi, Claudia Bonardi, Stefano Sartori, Andrea Berger, Dorota Hoffman‐Zacharska, Massimo Mastrangelo, Francesca Darra, Arve Vøllo, M. Mahdi Motazacker, Phillis Lakeman, Mathilde Nizon, Cornelia Betzler, Cécilia Altuzarra, Roseline Caume, Agathe Roubertie, Philippe Gélisse, Carla Marini, Renzo Guerrini, Frédéric Bilan, Daniel Tibussek, Margarete Koch‐Hogrebe, Μ. Scott Perry, Shoji Ichikawa, Е. Л. Дадали, Artem Sharkov, Irina Mishina, M. O. Abramov, Ilya Kanivets, С. А. Коростелев, Sergey I. Kutsev, Karen E. Wain, Nancy Eisenhauer, Monisa Wagner, Juliann M. Savatt, Karen Müller‐Schlüter, Haim Bassan, Artem Borovikov, Marie‐Cécile Nassogne

    Udgivet 2021
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