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Magdalena Chmara

Showing results (11-20 of 25) with videos related to

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Anticancer Research|March 2, 2005
Loss of heterozygosity at chromosomes 3p and 17p in primary non-small cell lung cancerMagdalena Chmara, Agnieszka Wozniak, Karolina Ochman, et al.
Scientific Reports|May 24, 2026
Association between CRP rs1800947 genotypes, dexamethasone use, postoperative CRP level and morbidity in adult cardiac surgical patients in post-hoc analysis of the observational INFLACOR cohort trialMaciej Michał Kowalik, Romuald Lango, Maciej Brzeziński, et al.
Journal of Atherosclerosis and Thrombosis|December 16, 2015
Assessment of Subclinical Atherosclerosis Using Computed Tomography Calcium Scores in Patients with Familial and Nonfamilial HypercholesterolemiaRafal Galaska, Dorota Kulawiak-Galaska, Agnieszka Wegrzyn, et al.
Journal of Applied Genetics|February 12, 2008
Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in the LDLR geneJolanta Kubalska, Magdalena Chmara, Janusz Limon, et al.
Journal of Clinical Medicine|September 9, 2023
Aortic Wall Thickness as a Surrogate for Subclinical Atherosclerosis in Familial and Nonfamilial Hypercholesterolemia: Quantitative 3D Magnetic Resonance Imaging Study and Interrelations with Computed Tomography Calcium Scores, and Carotid UltrasonographyRafał Gałąska, Dorota Kulawiak-Gałąska, Karolina Dorniak, et al.
Cardiology Journal|September 21, 2018
Long-term lipoprotein apheresis in the treatment of severe familial hypercholesterolemia refractory to high intensity statin therapy: Three year experience at a lipoprotein apheresis centreAgnieszka Mickiewicz, Justyna Borowiec-Wolna, Witold Bachorski, et al.
Life (Basel, Switzerland)|May 24, 2020
Higher Responsiveness to Rosuvastatin in Polygenic versus Monogenic Hypercholesterolaemia: A Propensity Score AnalysisAgnieszka Mickiewicz, Marta Futema, Agnieszka Ćwiklinska, et al.
Genes, Chromosomes & Cancer|May 1, 2013
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiencyMagdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, et al.
Atherosclerosis|April 11, 2016
Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in PolandAgnieszka Mickiewicz, Magdalena Chmara, Marta Futema, et al.
Human Mutation|November 6, 2007
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutationEllen Denayer, Annabel Parret, Magdalena Chmara, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Anticancer Research|March 2, 2005
Loss of heterozygosity at chromosomes 3p and 17p in primary non-small cell lung cancerMagdalena Chmara, Agnieszka Wozniak, Karolina Ochman, et al.
Scientific Reports|May 24, 2026
Association between CRP rs1800947 genotypes, dexamethasone use, postoperative CRP level and morbidity in adult cardiac surgical patients in post-hoc analysis of the observational INFLACOR cohort trialMaciej Michał Kowalik, Romuald Lango, Maciej Brzeziński, et al.
Journal of Atherosclerosis and Thrombosis|December 16, 2015
Assessment of Subclinical Atherosclerosis Using Computed Tomography Calcium Scores in Patients with Familial and Nonfamilial HypercholesterolemiaRafal Galaska, Dorota Kulawiak-Galaska, Agnieszka Wegrzyn, et al.
Journal of Applied Genetics|February 12, 2008
Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in the LDLR geneJolanta Kubalska, Magdalena Chmara, Janusz Limon, et al.
Journal of Clinical Medicine|September 9, 2023
Aortic Wall Thickness as a Surrogate for Subclinical Atherosclerosis in Familial and Nonfamilial Hypercholesterolemia: Quantitative 3D Magnetic Resonance Imaging Study and Interrelations with Computed Tomography Calcium Scores, and Carotid UltrasonographyRafał Gałąska, Dorota Kulawiak-Gałąska, Karolina Dorniak, et al.
Cardiology Journal|September 21, 2018
Long-term lipoprotein apheresis in the treatment of severe familial hypercholesterolemia refractory to high intensity statin therapy: Three year experience at a lipoprotein apheresis centreAgnieszka Mickiewicz, Justyna Borowiec-Wolna, Witold Bachorski, et al.
Life (Basel, Switzerland)|May 24, 2020
Higher Responsiveness to Rosuvastatin in Polygenic versus Monogenic Hypercholesterolaemia: A Propensity Score AnalysisAgnieszka Mickiewicz, Marta Futema, Agnieszka Ćwiklinska, et al.
Genes, Chromosomes & Cancer|May 1, 2013
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiencyMagdalena Chmara, Annekatrin Wernstedt, Bartosz Wasag, et al.
Atherosclerosis|April 11, 2016
Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in PolandAgnieszka Mickiewicz, Magdalena Chmara, Marta Futema, et al.
Human Mutation|November 6, 2007
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutationEllen Denayer, Annabel Parret, Magdalena Chmara, et al.
Pageof 3