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Št. zadetkov: 3
Gender disparity in lipid testing among over 0.5 million adults from Pakistan
Amjad Nawaz, Madeeha Khan, Quratul Ain, Muhammad Amjad, Jaka Šikonja, Hijab Batool, Mohammad Iqbal Khan, Urh Grošelj, Fouzia Sadiq
Izvirni znanstveni članek
Oznake: cardiovascular disease;dyslipidemia;gender disparity;lipid testing;opportunistic testing;Pakistan;
Background and aims: Dyslipidemia is the major risk factor for atherosclerotic cardiovascular disease (ASCVD); therefore, its early diagnosis and treatment is necessary. While previous studies in Pakistan focused on general lipid profiles, investigations into gender disparities in lipid testing rema ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Prevalence of familial hypercholesterolemia in Pakistan
Amjad Nawaz, Madeeha Khan, Quratul Ain, Jaka Šikonja, Hijab Batool, Muhammad Qasim Hayat, Mohammad Iqbal Khan, Urh Grošelj, Fouzia Sadiq
Izvirni znanstveni članek
Oznake: familial hypercholesterolemia;prevalence;cardiovascular disease;Pakistan;South Asia;Southeast Asia;screening;
Background: Familial hypercholesterolemia (FH) is an inherited disorder that causes elevated LDL-C levels leading to premature cardiovascular disease but remains underdiagnosed. This study aims to determine the prevalence of FH in Pakistan using data from multiple laboratory networks and compare it ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan
Quratul Ain, Matija Cevc, Tatiana Marusic, Jaka Šikonja, Fouzia Sadiq, Urša Šuštar, Matej Mlinarič, Jernej Kovač, Hijab Batool, Mohammad Iqbal Khan, Katarina Trebušak Podkrajšek, Barbara Jenko, Tadej Battelino, Zlatko Fras, Urh Grošelj
Izvirni znanstveni članek
Oznake: LPL;case series;hypertriglyceridemia;lipoprotein lipase;lipoprotein lipase deficiency;pancreatitis;
Introduction: Hypertriglyceridemia (HTG) is a complex disorder caused by genetic and environmental factors that frequently results from loss-of-function variants in the gene encoding lipoprotein lipase (LPL). Heterozygous patients have a range of symptoms, while homozygous LPL deficiency presents wi ...
Leto: 2024 Vir: Medicinska fakulteta (UL MF)
Št. zadetkov: 3
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