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Clemens Müller-Reible

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

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Lancet (London, England)|August 21, 2003
Regional lactate and carbon dioxide concentrations in a metabolic test for malignant hyperthermiaMartin Anetseder, Martin Hager, Clemens Müller-Reible, et al.
Vitamins and Hormones|April 1, 2008
The vitamin K cycleJohannes Oldenburg, Milka Marinova, Clemens Müller-Reible, et al.
Neuropediatrics|May 9, 2017
The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle DystrophiesWolfram Kress, Simone Rost, Konstantin Kolokotronis, et al.
Thrombosis and Haemostasis|September 13, 2007
Current pharmacogenetic developments in oral anticoagulation therapy: the influence of variant VKORC1 and CYP2C9 allelesJohannes Oldenburg, Carville G Bevans, Andreas Fregin, et al.
Seminars in Hematology|February 12, 2004
Environmental and genetic factors influencing inhibitor developmentJohannes Oldenburg, Jörg Schröder, Hans Hermann Brackmann, et al.
Anesthesiology|December 3, 2002
Positive malignant hyperthermia susceptibility in vitro test in a patient with mitochondrial myopathy and myoadenylate deaminase deficiencyRuth M Fricker, Thomas Raffelsberger, Sigrid Rauch-Shorny, et al.
Orphanet Journal of Rare Diseases|June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in GermanyKirsten König, Astrid Pechmann, Simone Thiele, et al.
Nucleic Acids Research|August 8, 2009
Detecting species-site dependencies in large multiple sequence alignmentsRoland Schwarz, Philipp N Seibel, Sven Rahmann, et al.
Orphanet Journal of Rare Diseases|February 15, 2013
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trialMaggie C Walter, Peter Reilich, Simone Thiele, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|February 23, 2017
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorderSören Merker, Andreas Reif, Georg C Ziegler, et al.
Pageof 1

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

Sort By:
Pageof 1
Lancet (London, England)|August 21, 2003
Regional lactate and carbon dioxide concentrations in a metabolic test for malignant hyperthermiaMartin Anetseder, Martin Hager, Clemens Müller-Reible, et al.
Vitamins and Hormones|April 1, 2008
The vitamin K cycleJohannes Oldenburg, Milka Marinova, Clemens Müller-Reible, et al.
Neuropediatrics|May 9, 2017
The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle DystrophiesWolfram Kress, Simone Rost, Konstantin Kolokotronis, et al.
Thrombosis and Haemostasis|September 13, 2007
Current pharmacogenetic developments in oral anticoagulation therapy: the influence of variant VKORC1 and CYP2C9 allelesJohannes Oldenburg, Carville G Bevans, Andreas Fregin, et al.
Seminars in Hematology|February 12, 2004
Environmental and genetic factors influencing inhibitor developmentJohannes Oldenburg, Jörg Schröder, Hans Hermann Brackmann, et al.
Anesthesiology|December 3, 2002
Positive malignant hyperthermia susceptibility in vitro test in a patient with mitochondrial myopathy and myoadenylate deaminase deficiencyRuth M Fricker, Thomas Raffelsberger, Sigrid Rauch-Shorny, et al.
Orphanet Journal of Rare Diseases|June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in GermanyKirsten König, Astrid Pechmann, Simone Thiele, et al.
Nucleic Acids Research|August 8, 2009
Detecting species-site dependencies in large multiple sequence alignmentsRoland Schwarz, Philipp N Seibel, Sven Rahmann, et al.
Orphanet Journal of Rare Diseases|February 15, 2013
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trialMaggie C Walter, Peter Reilich, Simone Thiele, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|February 23, 2017
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorderSören Merker, Andreas Reif, Georg C Ziegler, et al.
Pageof 1