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Research article

First published 2018-3

Statin Therapy and Risk of Diabetes Mellitus in Aging Patients With Heterozygous Familial Hypercholesterolemia or Familial Combined Hyperlipidemia: A 10-Year Follow-Up

Ioannis Skoumas, Nikolaos Ioakeimidis, Charalambos Vlachopoulos [...]

Angiology

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Brief report

First published 2017-9

Statin intolerance in heterozygous familial hypercolesterolemia with cardiovascular disease: After PCSK-9 antibodies what else?

Francesco Sbrana, Beatrice Dal Pino, Federico Bigazzi [...]

European Journal of Preventive Cardiology

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Research article

First published 2021-1

Lipoprotein Apheresis and Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors in Patients With Heterozygous Familial Hypercholesterolemia: A One Center Study

Vana Kolovou, Niki Katsiki, Stamatis Makrygiannis [...]

Journal of Cardiovascular Pharmacology and Therapeutics

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Research article

First published 2019-9

Risk of Ischemic Stroke and Peripheral Arterial Disease in Heterozygous Familial Hypercholesterolemia: A Meta-Analysis

Leo E. Akioyamen, Jack V. Tu, Jacques Genest [...]

Angiology

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Research article

First published 2013-01

Adeno-Associated Virus Serotype 8 Gene Therapy Leads to Significant Lowering of Plasma Cholesterol Levels in Humanized Mouse Models of Homozygous and Heterozygous Familial Hypercholesterolemia

Sadik H. Kassim, Hui Li, Peter Bell [...]

Human Gene Therapy

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Review article

First published 1999-01

Sonography of Achilles Tendon Xanthomas in Patients with Heterozygous Familial Hypercholesterolemia

Journal of Diagnostic Medical Sonography

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Research article

First published 1995-2

Treatment of Homozygous and Double Heterozygous Familial Hypercholesterolemia Children with LDL-Apheresis

C. Stefanutti, A. Vivenzio, C. Colombo [...]

The International Journal of Artificial Organs

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Research article

First published 2004-5

Clinical Management of Children and Young Adults with Heterozygous Familial Hypercholesterolaemia in the UK

Owen Greene, Paul Durrington

Journal of the Royal Society of Medicine

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Research article

First published 2017-7

Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia

Paolo Rubba, Marco Gentile, Gennaro Marotta [...]

European Journal of Preventive Cardiology

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Research article

First published 2019-06

Independent Severe Cases of Heterozygous Familial Hypercholesterolemia Caused by the W483X and Novel W483G Mutations in the Low-Density Lipoprotein Receptor Gene That Were Clinically Diagnosed as Homozygous Cases

Shitong Cheng, Yue Wu, Wenhui Wen [...]

Genetic Testing and Molecular Biomarkers

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