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Boris Rolinski

Showing results (1-10 of 18) with videos related to

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Journal of Separation Science|May 14, 2021
A new HPLC-MS/MS analytical method for quantification of tazobactam, piperacillin, and meropenem in human plasmaDušan Krnáč, Katarína Reiffová, Boris Rolinski
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|September 5, 2019
A new HPLC-MS/MS method for simultaneous determination of Cyclosporine A, Tacrolimus, Sirolimus and Everolimus for routine therapeutic drug monitoringDušan Krnáč, Katarína Reiffová, Boris Rolinski
Metabolic Brain Disease|February 8, 2012
Mimicry between mitochondrial disorder and multiple sclerosisJosef Finsterer, Romana Höftberger, Claudia Stöllberger, et al.
The Open Neurology Journal|February 21, 2017
Affection of the Respiratory Muscles in Combined Complex I and IV DeficiencyJosef Finsterer, Helmut Rauschka, Liane Segal, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 14, 2014
Presumed mitochondrial disease manifesting with recurrent syncopesJosef Finsterer, Romana Höftberger, Boris Rolinski, et al.
Biomedical Chromatography : BMC|April 18, 2023
Development and validation of a simple HPLC-MS/MS method for the quantification of methylmalonic acid in human serum without a derivatization stepSabrina Hofmann, Julian Gebauer, Dušan Krnáč, et al.
Pediatrics|April 6, 2006
Bilirubin measurement for neonates: comparison of 9 frequently used methodsKarina Grohmann, Markus Roser, Boris Rolinski, et al.
Clinical Biochemistry|May 1, 2007
Clinical validation of a new blood collection tube for the accuracy of total homocysteine measurement by different methodsEmmanuel Bissé, Thomas Epting, Gabriele Kögel, et al.
Human Mutation|May 14, 2008
Investigation of citrullinemia type I variants by in vitro expression studiesChristoph Berning, Iris Bieger, Silke Pauli, et al.
American Journal of Human Genetics|December 14, 2011
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathwayJohannes A Mayr, Peter Freisinger, Kurt Schlachter, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Separation Science|May 14, 2021
A new HPLC-MS/MS analytical method for quantification of tazobactam, piperacillin, and meropenem in human plasmaDušan Krnáč, Katarína Reiffová, Boris Rolinski
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|September 5, 2019
A new HPLC-MS/MS method for simultaneous determination of Cyclosporine A, Tacrolimus, Sirolimus and Everolimus for routine therapeutic drug monitoringDušan Krnáč, Katarína Reiffová, Boris Rolinski
Metabolic Brain Disease|February 8, 2012
Mimicry between mitochondrial disorder and multiple sclerosisJosef Finsterer, Romana Höftberger, Claudia Stöllberger, et al.
The Open Neurology Journal|February 21, 2017
Affection of the Respiratory Muscles in Combined Complex I and IV DeficiencyJosef Finsterer, Helmut Rauschka, Liane Segal, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|February 14, 2014
Presumed mitochondrial disease manifesting with recurrent syncopesJosef Finsterer, Romana Höftberger, Boris Rolinski, et al.
Biomedical Chromatography : BMC|April 18, 2023
Development and validation of a simple HPLC-MS/MS method for the quantification of methylmalonic acid in human serum without a derivatization stepSabrina Hofmann, Julian Gebauer, Dušan Krnáč, et al.
Pediatrics|April 6, 2006
Bilirubin measurement for neonates: comparison of 9 frequently used methodsKarina Grohmann, Markus Roser, Boris Rolinski, et al.
Clinical Biochemistry|May 1, 2007
Clinical validation of a new blood collection tube for the accuracy of total homocysteine measurement by different methodsEmmanuel Bissé, Thomas Epting, Gabriele Kögel, et al.
Human Mutation|May 14, 2008
Investigation of citrullinemia type I variants by in vitro expression studiesChristoph Berning, Iris Bieger, Silke Pauli, et al.
American Journal of Human Genetics|December 14, 2011
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathwayJohannes A Mayr, Peter Freisinger, Kurt Schlachter, et al.
Pageof 2