Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia-Reference-Cited by-同舟云学术

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

Published:2017-03-29 Issue:10 Volume:24 Page:1051-1059
ISSN:2047-4873
Container-title:European Journal of Preventive Cardiology
language:en
Short-container-title:Eur J Prev Cardiolog

Author:

Rubba Paolo¹,Gentile Marco¹,Marotta Gennaro¹,Iannuzzi Arcangelo²,Sodano Marta¹,De Simone Biagio¹,Jossa Fabrizio¹,Iannuzzo Gabriella¹,Giacobbe Carola³⁴,Di Taranto Maria D⁵,Fortunato Giuliana³⁴

Affiliation:

1. Dipartimento di Medicina Clinica e Chirurgia, Università ‘Federico II’ di Napoli, Italy

2. UO Medicina Interna, AORN ‘A Cardarelli’ di Napoli, Italy

3. CEINGE S.c.a r.l. Biotecnologie Avanzate, Napoli, Italy

4. Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Napoli, Italy

5. IRCCS Fondazione SDN, Napoli, Italy

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

Link

http://journals.sagepub.com/doi/pdf/10.1177/2047487317702040

Reference23 articles.

1. Familial Hypercholesterolemias: Prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia

2. The genetic architecture of the familial hyperlipidaemia syndromes

3. A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia

4. 2016 ESC/EAS Guidelines for the Management of Dyslipidaemias

5. Efficacy and Safety of Alirocumab in Reducing Lipids and Cardiovascular Events

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