检索结果 - C. R. Müller

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  1. 1
    On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.

    On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis. 由 T. Grimm, Gerhard Meng, Sabina Liechti‐Gallati, T. Bettecken, C R Müller, B. Müller

    出版 1994
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  2. 2
    Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment

    Thirteen novel VKORC1 mutations associated with oral anticoagulant resistance: insights into improved patient diagnosis and treatment 由 Matthias Watzka, Christof Geisen, Carville G. Bevans, Katja Sittinger, Gabriele Spohn, Simone Rost, E. Seifried, C. R. Müller, Johannes Oldenburg

    出版 2010
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  3. 3
    Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia Group

    Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia Group 由 Klaus P.E. Glahn, F.R. ELLIS, P.J. Halsall, C. R. Müller, M.M.J. Snoeck, A. Urwyler, Frank Wappler

    出版 2010
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  4. 4
    European Malignant Hyperthermia Group guidelines for investigation of malignant hyperthermia susceptibility

    European Malignant Hyperthermia Group guidelines for investigation of malignant hyperthermia susceptibility 由 Philip M. Hopkins, Henrik Rüffert, M.M.J. Snoeck, Thierry Girard, Klaus P.E. Glahn, F.R. ELLIS, C. R. Müller, A. Urwyler

    出版 2015
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  5. 5
    Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

    Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies 由 Haiyan Zhou, Heinz Jungbluth, C. Sewry, Longhua Feng, Enrico Bertini, K. Bushby, Volker Straub, H. Roper, Michael R. Rose, Martin Brockington, Maria Kinali, Adnan Manzur, S. Robb, Richard Appleton, Sonia Messina, Adele D'Amico, Rosaline C. M. Quinlivan, Michael Swash, C. R. Müller, S. Brown, Susan Treves, Francesco Muntoni

    出版 2007
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  6. 6
    <i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei

    <i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei 由 Jo M. Wilmshurst, Suzanne Lillis, Haiyan Zhou, Komala Pillay, Heather Henderson, Wolfram Kreß, C. R. Müller, Alvin Ndondo, V. Cloke, Thomas Cullup, Enrico Bertini, C. Boennemann, Volker Straub, Rosaline C. M. Quinlivan, James J. Dowling, Safa Al Sarraj, Susan Treves, Stephen Abbs, Adnan Y. Manzur, Caroline A. Sewry, Francesco Muntoni, Heinz Jungbluth

    出版 2010
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