Coronary artery disease in a child with homozygous familial hypercholesterolemia: Regression after liver transplantation
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference36 articles.
1. Homozygous familial hypercholesterolemia: case series and review of the literature;Palacio;Case Rep Transplant,2011
2. Liver transplantation for HoFH in children: single center experience;Cephus;Congenit Heart Dis,2015
3. Familial hypercholesterolemia: report of coronary death at age 3 in a homozygous child and prenatal diagnosis in a heterozygous sibling;Rose;J Pediatr,1982
4. Liver transplantation in a subject with familial hypercholesterolemia carrying the homozygous p.W577R LDL-receptor gene mutation;Schmidt;Clin Transplant,2008
5. Familial hypercholesterolemia – epidemiology, diagnosis and screening;Singh;Curr Atheroscler Rep,2015
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1. N-SREBP2 Provides a Mechanism for Dynamic Control of Cellular Cholesterol Homeostasis;Cells;2024-07-25
2. Clinical practice recommendations on lipoprotein apheresis for children with homozygous familial hypercholesterolaemia: An expert consensus statement from ERKNet and ESPN;Atherosclerosis;2024-05
3. Clinical practice recommendations on lipoprotein apheresis for children with homozygous familial hypercholesterolemia: an expert consensus statement from ERKNet and ESPN;2023-11-15
4. International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia;Nature Reviews Cardiology;2023-06-15
5. 2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance;European Heart Journal;2023-05-02
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