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Clemens R Müller

Showing results (1-10 of 40) with videos related to

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Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|November 18, 2009
[Malignant hyperthermia--diagnostics, treatment and anaesthetic management]Frank Schuster, Clemens R Müller-Reible
Molecular Genetics and Metabolism|June 8, 2002
Alkaptonuria in Slovakia: thirty-two years of research on phenotype and genotypeStefan Srsen, Clemens R Müller, Andreas Fregin, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 26, 2005
[Malignant hyperthermia--a hereditary and potentially life-threatening condition]Tonje Haugen, Mathias Toft, Clemens R Müller, et al.
Thrombosis and Haemostasis|November 25, 2010
Identification of VKORC1 interaction partners by split-ubiquitin system and coimmunoprecipitationAnne Schaafhausen, Simone Rost, Johannes Oldenburg, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
Risk assessment and genetic counseling in families with Duchenne muscular dystrophyTiemo Grimm, Wolfram Kress, Gerhard Meng, et al.
Lancet (London, England)|June 6, 2002
Diagnosis of susceptibility to malignant hyperthermia by use of a metabolic testMartin Anetseder, Martin Hager, Clemens R Müller, et al.
Antioxidants & Redox Signaling|May 9, 2006
Vitamin K epoxide reductase complex subunit 1 (VKORC1): the key protein of the vitamin K cycleJohannes Oldenburg, Carville G Bevans, Clemens R Müller, et al.
BMC Genetics|February 5, 2014
Confirmation of warfarin resistance of naturally occurring VKORC1 variants by coexpression with coagulation factor IX and in silico protein modellingElisabeth Müller, Alexander Keller, Andreas Fregin, et al.
European Journal of Cell Biology|July 11, 2009
Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA geneSebastian Kandert, Manfred Wehnert, Clemens R Müller, et al.
Thrombosis and Haemostasis|May 8, 2015
Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII geneJ Elisa Bach, Beat Wolf, Johannes Oldenburg, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|November 18, 2009
[Malignant hyperthermia--diagnostics, treatment and anaesthetic management]Frank Schuster, Clemens R Müller-Reible
Molecular Genetics and Metabolism|June 8, 2002
Alkaptonuria in Slovakia: thirty-two years of research on phenotype and genotypeStefan Srsen, Clemens R Müller, Andreas Fregin, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 26, 2005
[Malignant hyperthermia--a hereditary and potentially life-threatening condition]Tonje Haugen, Mathias Toft, Clemens R Müller, et al.
Thrombosis and Haemostasis|November 25, 2010
Identification of VKORC1 interaction partners by split-ubiquitin system and coimmunoprecipitationAnne Schaafhausen, Simone Rost, Johannes Oldenburg, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
Risk assessment and genetic counseling in families with Duchenne muscular dystrophyTiemo Grimm, Wolfram Kress, Gerhard Meng, et al.
Lancet (London, England)|June 6, 2002
Diagnosis of susceptibility to malignant hyperthermia by use of a metabolic testMartin Anetseder, Martin Hager, Clemens R Müller, et al.
Antioxidants & Redox Signaling|May 9, 2006
Vitamin K epoxide reductase complex subunit 1 (VKORC1): the key protein of the vitamin K cycleJohannes Oldenburg, Carville G Bevans, Clemens R Müller, et al.
BMC Genetics|February 5, 2014
Confirmation of warfarin resistance of naturally occurring VKORC1 variants by coexpression with coagulation factor IX and in silico protein modellingElisabeth Müller, Alexander Keller, Andreas Fregin, et al.
European Journal of Cell Biology|July 11, 2009
Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA geneSebastian Kandert, Manfred Wehnert, Clemens R Müller, et al.
Thrombosis and Haemostasis|May 8, 2015
Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII geneJ Elisa Bach, Beat Wolf, Johannes Oldenburg, et al.
Pageof 4