A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry).

doi:10.1016/j.atherosclerosis.2018.01.034

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Article

A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry).

Atherosclerosis - 1 Mar 2018

Kayikcioglu Meral, Tokgozoglu Lale, Yilmaz Mehmet, Kaynar Leylagul, Aktan Melih, Durmuş Rana Berru, Gokce Cumali, Temizhan Ahmet, Ozcebe Osman Ilhami, Akyol Tulay Karaagac, Okutan Harika, Sag Saim, Gul Ozen Oz, Salcioglu Zafer, Yenercag Mustafa, Altunkeser Bulent B, Kuku Irfan, Yasar Hamiyet Yilmaz, Kurtoglu Erdal, Kose Melis Demir, Demircioglu Sinan, Pekkolay Zafer, Ilhan Osman

Abstract excerpt

BACKGROUND AND AIMS: Homozygous familial hypercholesterolemia (HoFH) is a genetic condition characterized by lethally high levels of low-density lipoprotein cholesterol (LDL-C) from birth, and requires rapid and aggressive intervention to prevent death due to coronary heart disease and/or atherosclerosis. Where available, lipoprotein apheresis (LA) is the mainstay of treatment to promote survival. METHODS: A-HIT1...

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PMID: 29407887
DOI: 10.1016/j.atherosclerosis.2018.01.034

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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