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Adam D McIntyre

Showing results (11-20 of 67) with videos related to

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Paediatrics & Child Health|January 15, 2015
A novel MC4R mutation associated with childhood-onset obesity: A case reportManpreet Doulla, Adam D McIntyre, Robert A Hegele, et al.
Genes|January 25, 2025
Lipoprotein Lipase: Structure, Function, and Genetic VariationShehan D Perera, Jian Wang, Adam D McIntyre, et al.
Journal of Clinical Lipidology|December 7, 2016
Familial partial lipodystrophy presenting as metabolic syndromeDarwin Chan, Adam D McIntyre, Robert A Hegele, et al.
Journal of Clinical Lipidology|July 4, 2025
Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemiaShyann Hang, Jian Wang, Zahra Taboun, et al.
CJC Open|January 16, 2026
Spectrum of DNA Variants in Southwestern Ontario Patients with Familial HypercholesterolemiaSanaz Lordfard, Jian Wang, Adam D McIntyre, et al.
Journal of Clinical Lipidology|February 9, 2020
The polygenic nature of mild-to-moderate hypertriglyceridemiaJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
The Journal of Clinical Endocrinology and Metabolism|September 5, 2024
Comparison of Patients With Familial Chylomicronemia Syndrome and Multifactorial Chylomicronemia SyndromeCatherine M Spagnuolo, Jian Wang, Adam D McIntyre, et al.
Journal of Clinical Lipidology|December 8, 2022
The longitudinal triglyceride phenotype in heterozygotes with LPL pathogenic variantsShehan D Perera, Jian Wang, Adam D McIntyre, et al.
Journal of Investigative Medicine High Impact Case Reports|July 20, 2018
A De Novo <i>POLD1</i> Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner SyndromeLinda R Wang, Aleksandar Radonjic, Allison A Dilliott, et al.
Journal of Clinical Lipidology|January 17, 2021
Interrogation of selected genes influencing serum LDL-Cholesterol levels in patients with well characterized NAFLDEduardo Vilar-Gomez, Samer Gawrieh, Tiebing Liang, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
Paediatrics & Child Health|January 15, 2015
A novel MC4R mutation associated with childhood-onset obesity: A case reportManpreet Doulla, Adam D McIntyre, Robert A Hegele, et al.
Genes|January 25, 2025
Lipoprotein Lipase: Structure, Function, and Genetic VariationShehan D Perera, Jian Wang, Adam D McIntyre, et al.
Journal of Clinical Lipidology|December 7, 2016
Familial partial lipodystrophy presenting as metabolic syndromeDarwin Chan, Adam D McIntyre, Robert A Hegele, et al.
Journal of Clinical Lipidology|July 4, 2025
Heterozygous pathogenic PPARG variants in patients with severe hypertriglyceridemiaShyann Hang, Jian Wang, Zahra Taboun, et al.
CJC Open|January 16, 2026
Spectrum of DNA Variants in Southwestern Ontario Patients with Familial HypercholesterolemiaSanaz Lordfard, Jian Wang, Adam D McIntyre, et al.
Journal of Clinical Lipidology|February 9, 2020
The polygenic nature of mild-to-moderate hypertriglyceridemiaJacqueline S Dron, Jian Wang, Adam D McIntyre, et al.
The Journal of Clinical Endocrinology and Metabolism|September 5, 2024
Comparison of Patients With Familial Chylomicronemia Syndrome and Multifactorial Chylomicronemia SyndromeCatherine M Spagnuolo, Jian Wang, Adam D McIntyre, et al.
Journal of Clinical Lipidology|December 8, 2022
The longitudinal triglyceride phenotype in heterozygotes with LPL pathogenic variantsShehan D Perera, Jian Wang, Adam D McIntyre, et al.
Journal of Investigative Medicine High Impact Case Reports|July 20, 2018
A De Novo <i>POLD1</i> Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner SyndromeLinda R Wang, Aleksandar Radonjic, Allison A Dilliott, et al.
Journal of Clinical Lipidology|January 17, 2021
Interrogation of selected genes influencing serum LDL-Cholesterol levels in patients with well characterized NAFLDEduardo Vilar-Gomez, Samer Gawrieh, Tiebing Liang, et al.
Pageof 7