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Christian Geier

Showing results (41-50 of 46) with videos related to

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Human Mutation|April 15, 2008
A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathySiv Fokstuen, Robert Lyle, Analia Munoz, et al.
Rheumatology International|November 1, 2021
Tumor necrosis factor inhibitor (TNFi) persistence and reasons for discontinuation in a predominantly male cohort with axial spondyloarthritisDelamo I Bekele, Elizabeth Cheng, Andreas Reimold, et al.
Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.
Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
European Heart Journal|October 14, 2017
Clinical genetics and outcome of left ventricular non-compaction cardiomyopathyFarbod Sedaghat-Hamedani, Jan Haas, Feng Zhu, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Human Mutation|April 15, 2008
A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathySiv Fokstuen, Robert Lyle, Analia Munoz, et al.
Rheumatology International|November 1, 2021
Tumor necrosis factor inhibitor (TNFi) persistence and reasons for discontinuation in a predominantly male cohort with axial spondyloarthritisDelamo I Bekele, Elizabeth Cheng, Andreas Reimold, et al.
Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.
Human Molecular Genetics|May 29, 2008
Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathyChristian Geier, Katja Gehmlich, Elisabeth Ehler, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
European Heart Journal|October 14, 2017
Clinical genetics and outcome of left ventricular non-compaction cardiomyopathyFarbod Sedaghat-Hamedani, Jan Haas, Feng Zhu, et al.
Pageof 5