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Matej Mlinaric

Showing results (11-20 of 24) with videos related to

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Atherosclerosis|August 21, 2025
Sex differences in cholesterol levels among prepubertal childrenJan Kafol, Mia Becker, Barbara Cugalj Kern, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2022
Universal screening for familial hypercholesterolemia in 2 populationsUrsa Sustar, Olga Kordonouri, Matej Mlinaric, et al.
Frontiers in Genetics|October 23, 2020
Genetic and Clinical Characteristics of Patients With Homozygous and Compound Heterozygous Familial Hypercholesterolemia From Three Different Populations: Case SeriesTatiana Marusic, Ursa Sustar, Fouzia Sadiq, et al.
Frontiers in Endocrinology|June 26, 2024
Case report: The success of empagliflozin therapy for glycogen storage disease type 1bAna Klinc, Urh Groselj, Matej Mlinaric, et al.
Atherosclerosis|February 18, 2026
LDLR and APOB pathogenic variants predict discordant TSH effect on LDL-CJan Kafol, Jaka Sikonja, Matej Mlinaric, et al.
American Journal of Preventive Cardiology|June 30, 2025
Enhanced oral glucose tolerance test for early detection of insulin resistance and metabolic complications in children with obesityUrh Groselj, Jan Kafol, Jaka Sikonja, et al.
Atherosclerosis Plus|May 25, 2026
Parallel screening strategies reveal distinct phenotypic and genotypic profiles of familial hypercholesterolemia in children and adultsJaka Sikonja, Urska Intihar, Borut Jug, et al.
European Journal of Preventive Cardiology|June 27, 2025
Proposal of a Familial Hypercholesterolemia Pediatric Diagnostic Score (FH-PeDS)Jan Kafol, Beatriz Miranda, Rok Sikonja, et al.
Frontiers in Endocrinology|June 24, 2024
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature reviewQuratul Ain, Matija Cevc, Tatiana Marusic, et al.
Molecular Genetics and Metabolism Reports|February 2, 2026
Branched-chain amino acid transferase 2 (BCAT2) deficiency: A case series and systematic reviewMaja Filipic, Ziga Iztok Remec, Ana Drole Torkar, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Atherosclerosis|August 21, 2025
Sex differences in cholesterol levels among prepubertal childrenJan Kafol, Mia Becker, Barbara Cugalj Kern, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 1, 2022
Universal screening for familial hypercholesterolemia in 2 populationsUrsa Sustar, Olga Kordonouri, Matej Mlinaric, et al.
Frontiers in Genetics|October 23, 2020
Genetic and Clinical Characteristics of Patients With Homozygous and Compound Heterozygous Familial Hypercholesterolemia From Three Different Populations: Case SeriesTatiana Marusic, Ursa Sustar, Fouzia Sadiq, et al.
Frontiers in Endocrinology|June 26, 2024
Case report: The success of empagliflozin therapy for glycogen storage disease type 1bAna Klinc, Urh Groselj, Matej Mlinaric, et al.
Atherosclerosis|February 18, 2026
LDLR and APOB pathogenic variants predict discordant TSH effect on LDL-CJan Kafol, Jaka Sikonja, Matej Mlinaric, et al.
American Journal of Preventive Cardiology|June 30, 2025
Enhanced oral glucose tolerance test for early detection of insulin resistance and metabolic complications in children with obesityUrh Groselj, Jan Kafol, Jaka Sikonja, et al.
Atherosclerosis Plus|May 25, 2026
Parallel screening strategies reveal distinct phenotypic and genotypic profiles of familial hypercholesterolemia in children and adultsJaka Sikonja, Urska Intihar, Borut Jug, et al.
European Journal of Preventive Cardiology|June 27, 2025
Proposal of a Familial Hypercholesterolemia Pediatric Diagnostic Score (FH-PeDS)Jan Kafol, Beatriz Miranda, Rok Sikonja, et al.
Frontiers in Endocrinology|June 24, 2024
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature reviewQuratul Ain, Matija Cevc, Tatiana Marusic, et al.
Molecular Genetics and Metabolism Reports|February 2, 2026
Branched-chain amino acid transferase 2 (BCAT2) deficiency: A case series and systematic reviewMaja Filipic, Ziga Iztok Remec, Ana Drole Torkar, et al.
Pageof 3