Diagnostic and Therapeutic Challenges of Homozygous and Severe Heterozygous Familial Hypercholesterolemia from Clinical Aspect-A Single-Center Study. [PDF]
Nádró B +5 more
europepmc +1 more source
Cascade Screening and Treatment Initiation in Young Adults with Heterozygous Familial Hypercholesterolemia. [PDF]
Peterson AL +4 more
europepmc +1 more source
Real-World Experience from Türkiye: Genetic and Therapeutic Insights in Pediatric Heterozygous Familial Hypercholesterolemia [PDF]
Yazıcı H +12 more
europepmc +1 more source
Efficacy and safety of tafolecimab in Chinese patients with heterozygous familial hypercholesterolemia: a randomized, double-blind, placebo-controlled phase 3 trial (CREDIT-2). [PDF]
Chai M +17 more
europepmc +1 more source
Statins for children with familial hypercholesterolemia
Background: Familial hypercholesterolemia is one of the most common inherited metabolic diseases and is an autosomal dominant disorder meaning heterozygotes, or carriers, are affected. Those who are homozygous have severe disease.
Vuorio, A. +7 more
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Cataract Surgery in Elderly Subjects with Heterozygous Familial Hypercholesterolemia in Prolonged Treatment with Statins. [PDF]
Marco-Benedí V +6 more
europepmc +1 more source
Oral Porphyromonas gingivalis and Fusobacterium nucleatum Abundance in Subjects in Primary and Secondary Cardiovascular Prevention, with or without Heterozygous Familial Hypercholesterolemia. [PDF]
Curia MC +10 more
europepmc +1 more source
Glucose metabolism in heterozygous familial hypercholesterolemia with a founder effect and a high diabetes prevalence: a cross-sectional study. [PDF]
González-Lleó AM +14 more
europepmc +1 more source
Myocardial fibrosis assessed by magnetic resonance imaging in asymptomatic heterozygous familial hypercholesterolemia: the cholcoeur study. [PDF]
Gallo A +16 more
europepmc +1 more source
Apparent Nonresponse to PCSK9 Inhibition in a Patient With Heterozygous Familial Hypercholesterolemia Due to PCSK9 Gene Duplication. [PDF]
Pindwarawala M, Bose S, Brunham LR.
europepmc +1 more source

