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Georg Klein

Showing results (31-40 of 51) with videos related to

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Therapeutic Drug Monitoring|March 25, 2009
Pharmacokinetics of mycophenolic acid and its glucuronide metabolites in stable adult liver transplant recipients with renal dysfunction on a low-dose calcineurin inhibitor regimen and mycophenolate mofetilSusanne Beckebaum, Victor W Armstrong, Vito Rosario Cicinnati, et al.
Plos One|December 24, 2008
Strong association of a common dihydropyrimidine dehydrogenase gene polymorphism with fluoropyrimidine-related toxicity in cancer patientsEva Gross, Birgit Busse, Matthias Riemenschneider, et al.
Genome Research|September 27, 2013
Large-scale hypomethylated blocks associated with Epstein-Barr virus-induced B-cell immortalizationKasper D Hansen, Sarven Sabunciyan, Ben Langmead, et al.
Croatian Medical Journal|January 9, 2018
Severe bleeding complications and multiple kidney transplants in a patient with tuberous sclerosis complex caused by a novel TSC2 missense variantStela Živčić-Ćosić, Karin Mayer, Gordana Đorđević, et al.
European Journal of Medical Genetics|January 18, 2019
Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providersAlexandra Benachi, Jessica Caffrey, Pavel Calda, et al.
Gene|March 12, 2013
Expanding the mutation spectrum for Fraser syndrome: identification of a novel heterozygous deletion in FRAS1Julia Hoefele, Christian Wilhelm, Monika Schiesser, et al.
Gene|June 5, 2013
Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndromeSonja Beicht, Gertrud Strobl-Wildemann, Sabine Rath, et al.
Annals of Transplantation|December 17, 2013
Compliance and tolerability of subcutaneous hepatitis B immunoglobulin self-administration in liver transplant patients: a prospective, observational, multicenter studyChristian Georg Klein, Vito Cicinnati, Hartmut Schmidt, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous resultsKorbinian M Riedhammer, Patrick Richthammer, Dominik S Westphal, et al.
Genes|January 26, 2021
Novel <i>KCNH1</i> Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of <i>KCNH1</i>-Associated DiseasesRandi von Wrede, Monika Jeub, Idil Ariöz, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Therapeutic Drug Monitoring|March 25, 2009
Pharmacokinetics of mycophenolic acid and its glucuronide metabolites in stable adult liver transplant recipients with renal dysfunction on a low-dose calcineurin inhibitor regimen and mycophenolate mofetilSusanne Beckebaum, Victor W Armstrong, Vito Rosario Cicinnati, et al.
Plos One|December 24, 2008
Strong association of a common dihydropyrimidine dehydrogenase gene polymorphism with fluoropyrimidine-related toxicity in cancer patientsEva Gross, Birgit Busse, Matthias Riemenschneider, et al.
Genome Research|September 27, 2013
Large-scale hypomethylated blocks associated with Epstein-Barr virus-induced B-cell immortalizationKasper D Hansen, Sarven Sabunciyan, Ben Langmead, et al.
Croatian Medical Journal|January 9, 2018
Severe bleeding complications and multiple kidney transplants in a patient with tuberous sclerosis complex caused by a novel TSC2 missense variantStela Živčić-Ćosić, Karin Mayer, Gordana Đorđević, et al.
European Journal of Medical Genetics|January 18, 2019
Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providersAlexandra Benachi, Jessica Caffrey, Pavel Calda, et al.
Gene|March 12, 2013
Expanding the mutation spectrum for Fraser syndrome: identification of a novel heterozygous deletion in FRAS1Julia Hoefele, Christian Wilhelm, Monika Schiesser, et al.
Gene|June 5, 2013
Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndromeSonja Beicht, Gertrud Strobl-Wildemann, Sabine Rath, et al.
Annals of Transplantation|December 17, 2013
Compliance and tolerability of subcutaneous hepatitis B immunoglobulin self-administration in liver transplant patients: a prospective, observational, multicenter studyChristian Georg Klein, Vito Cicinnati, Hartmut Schmidt, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous resultsKorbinian M Riedhammer, Patrick Richthammer, Dominik S Westphal, et al.
Genes|January 26, 2021
Novel <i>KCNH1</i> Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of <i>KCNH1</i>-Associated DiseasesRandi von Wrede, Monika Jeub, Idil Ariöz, et al.
Pageof 6