Search Results - Claes Möller

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  1. 1
    Usher Syndrome

    Usher Syndrome by Alessandro Castiglione, Claes Möller

    Published 2022
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  2. 2
    Headphone listening habits and hearing thresholds in swedish adolescents

    Headphone listening habits and hearing thresholds in swedish adolescents by StephenE Widén, Sara Båsjö, Claes Möller, Kim Kähäri

    Published 2017
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  3. 3
    The ICF core sets for hearing loss project: International expert survey on functioning and disability of adults with hearing loss using the international classification of functioning, disability, and health (ICF)

    The ICF core sets for hearing loss project: International expert survey on functioning and disability of adults with hearing loss using the international classification of function... by Sarah Granberg, De Wet Swanepoel, Ulrika Englund, Claes Möller, Berth Danermark

    Published 2014
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  4. 4
    Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II

    Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II by Michael D. Weston, Mirjam W.J. Luijendijk, Kurt Humphrey, Claes Möller, William J. Kimberling

    Published 2004
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  5. 5
    The ICF core sets for hearing loss project: Functioning and disability from the patient perspective

    The ICF core sets for hearing loss project: Functioning and disability from the patient perspective by Sarah Granberg, Marieke Pronk, De Wet Swanepoel, Sophia E. Kramer, Hanna Hagsten, Jennie Hjaldahl, Claes Möller, Berth Danermark

    Published 2014
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  6. 6
    Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations

    Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations by Randall R. Fields, Guimei Zhou, Dali Huang, Jack R. Davis, Claes Möller, Samuel G. Jacobson, William J. Kimberling, János Sümegi

    Published 2002
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  7. 7
    Identification of p.A684V missense mutation in the <i>WFS1</i> gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

    Identification of p.A684V missense mutation in the <i>WFS1</i> gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment by Nanna Dahl Rendtorff, Marianne Lodahl, Houda Boulahbel, Ida R. Johansen, Arti Pandya, Katherine O. Welch, Virginia W. Norris, Kathleen S. Arnos, Maria Bitner‐Glindzicz, Sarah B. Emery, Marilyn B. Mets, Toril Fagerheim, Kristina Eriksson, Lars Hestbjerg Hansen, Helene Bruhn, Claes Möller, Sture Lindholm, Stefan Ensgaard, Marci M. Lesperance, Lisbeth Tranebjærg

    Published 2011
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  8. 8
    The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

    The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey by Ayşegül Ozantürk, Jan D. Marshall, Gayle B. Collin, Selma Düzenli, Robert Percy Marshall, Şükrü Candan, Tülay Tos, İhsan Esen, Mustafa Taşkesen, Atilla Çayır, Şükrü Öztürk, İhsan Üstün, Esra Ataman, Emin Karaca, Taha Reşid Özdemir, İlknur Erol, Fehime Kara Eroğlu, Deniz Torun, Erhan Parıltay, Elif Yılmaz Güleç, Ender Karaca, Mehmet Emre Atabek, Nursel Elçioğlu, İlhan Satman, Claes Möller, Jean Muller, Jürgen Κ. Naggert, Rıza Köksal Özgül

    Published 2014
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  9. 9
    CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

    CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness by Lisa M. Astuto, Julie M. Bork, Michael D. Weston, James W. Askew, Randall R. Fields, Dana J. Orten, S.J. Ohliger, Saima Riazuddin, Robert J. Morell, Shahid Y. Khan, Saima Riazuddin, Hannie Kremer, Peter Van Hauwe, Claes Möller, Cor W. R. J. Cremers, Carmen Ayuso, John R. Heckenlively, Klaus Rohrschneider, U.H. Spandau, Jacquie Greenberg, Raj Ramesar, William Reardon, Pierre Bitoun, Jesús Millán, Richard H. Legge, Thomas B. Friedman, William J. Kimberling

    Published 2002
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  10. 10
    High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

    High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH by Carl E.G. Bruder, Carina Hirvelä, Isabel Tapia‐Páez, Ingegerd Fransson, Richard Segraves, Greg Hamilton, Xiao Zhang, D. Gareth Evans, Andrew Wallace, Michael E. Baser, Jessica Zucman‐Rossi, Martin Hergersberg, Eugene Boltshauser, Laura Papi, Guy A. Rouleau, G. Poptodorov, Albena Jordanova, Helge Rask‐Andersen, Lan Kluwe, Victor Mautner, Markku Sainio, Gene Hung, Tiit Mathiesen, Claes Möller, Stefan M. Pulst, Henrik Harder, Arvid Heiberg, Mariko Honda, Michihito Niimura, Sigrid Sahlén, Elisabeth Blennow, Donna G. Albertson, Daniel Pinkel, Jan P. Dumanski

    Published 2001
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