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Efficacy and Safety of Pitavastatin in Children and Adolescents at High Future Cardiovascular Risk

The Journal of pediatrics, 2015-08, Vol.167 (2), p.338-343.e5

2015

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A 3-year study of atorvastatin in children and adolescents with heterozygous familial hypercholesterolemia

Journal of clinical lipidology, 2016-09, Vol.10 (5), p.1153-1162.e3

2016

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Genetic causes of monogenic familial hypercholesterolemia in the Greek population: Lessons, mistakes, and the way forward

Journal of clinical lipidology, 2016-07, Vol.10 (4), p.748-756

2016

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Molecular findings of monogenic familial hypercholesterolemia in the Greek population

Atherosclerosis, 2017-08, Vol.263, p.e225-e225

2017

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Statins for children with familial hypercholesterolemia

Cochrane database of systematic reviews, 2019-11, Vol.2019 (11)

2019

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Familial Hypercholesterolemia in Greek children and their families: Genotype-to-phenotype correlations and a reconsideration of LDLR mutation spectrum

Atherosclerosis, 2014-12, Vol.237 (2), p.798-804

2014

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Statins for children with familial hypercholesterolemia

Cochrane database of systematic reviews, 2017-07, Vol.7 (7), p.CD006401

2017

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A 3-YEAR OPEN-LABEL STUDY OF ATORVASTATIN IN CHILDREN AND ADOLESCENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

Journal of the American College of Cardiology, 2016-04, Vol.67 (13), p.1978-1978

2016

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A 3-YEAR OPEN-LABEL STUDY OF ATORVASTATIN IN CHILDREN AND ADOLESCENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

Journal of the American College of Cardiology, 2016-04, Vol.67 (13), p.1978-1978

2016

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The effect of Lp(a) on cardiovascular function in greek pediatric population 6-16 years old. Preliminary findings in children with or without familial hypercholesterolemia

Atherosclerosis, 2017-08, Vol.263, p.e207-e208

2017

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Late onset lysosomal acid lipase deficiency (LAL-D): successful outcome of five pregnancies from four homozygous women in Greece

Atherosclerosis, 2017-08, Vol.263, p.e224-e225

2017

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Molecular analysis of 15 homozygous LAL-D patients from greece using DBS screening

Atherosclerosis, 2017-08, Vol.263, p.e100-e101

2017

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Statins for children with familial hypercholesterolemia

Cochrane database of systematic reviews, 2014-07 (7), p.CD006401-CD006401

2014

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Novel LDLR Variants in Patients with Familial Hypercholesterolemia: In Silico Analysis as a Tool to Predict Pathogenic Variants in Children and Their Families

Annals of human genetics, 2013-09, Vol.77 (5), p.426-434

2013

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Toward an international consensus—Integrating lipoprotein apheresis and new lipid-lowering drugs

Journal of clinical lipidology, 2017-07, Vol.11 (4), p.858-871.e3

2017

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Analysis of LDLR mutations in familial hypercholesterolemia patients in Greece by use of the NanoChip® Microelectronic Array Technology

Clinica chimica acta, 2006-12, Vol.374 (1), p.93-99

2006

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Novel LDLR Variants in Patients with Familial Hypercholesterolemia: In Silico Analysis as a Tool to Predict Pathogenic Variants in Children and Their Families: In Silico Analysis of Novel LDLR Variants

Annals of human genetics, 2013-09, Vol.77 (5), p.426-434

2013

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POR28 SNP is associated with lipid response to atorvastatin in children and adolescents with familial hypercholesterolemia

Pharmacogenomics, 2014-12, Vol.15 (16), p.1963-1972

2014

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Development of a universal chemiluminometric genotyping method for high-throughput detection of 7 LDLR gene mutations in greek population

Clinical biochemistry, 2008-03, Vol.41 (4), p.335-342

2008

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Neutral lipid storage disease—response to dietary intervention

Archives of disease in childhood, 1997-08, Vol.77 (2), p.183-183

1997

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Hyperlipoproteinemia Type Ii - Genetics
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Receptors, Ldl - Genetics
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Familial Hypercholesterolemia
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Efficacy and Safety of Pitavastatin in Children and Adolescents at High Future Cardiovascular Risk

A 3-year study of atorvastatin in children and adolescents with heterozygous familial hypercholesterolemia

Genetic causes of monogenic familial hypercholesterolemia in the Greek population: Lessons, mistakes, and the way forward

Molecular findings of monogenic familial hypercholesterolemia in the Greek population

Statins for children with familial hypercholesterolemia

Familial Hypercholesterolemia in Greek children and their families: Genotype-to-phenotype correlations and a reconsideration of LDLR mutation spectrum

Statins for children with familial hypercholesterolemia

A 3-YEAR OPEN-LABEL STUDY OF ATORVASTATIN IN CHILDREN AND ADOLESCENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

A 3-YEAR OPEN-LABEL STUDY OF ATORVASTATIN IN CHILDREN AND ADOLESCENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA

The effect of Lp(a) on cardiovascular function in greek pediatric population 6-16 years old. Preliminary findings in children with or without familial hypercholesterolemia

Late onset lysosomal acid lipase deficiency (LAL-D): successful outcome of five pregnancies from four homozygous women in Greece

Molecular analysis of 15 homozygous LAL-D patients from greece using DBS screening

Statins for children with familial hypercholesterolemia

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

Novel LDLR Variants in Patients with Familial Hypercholesterolemia: In Silico Analysis as a Tool to Predict Pathogenic Variants in Children and Their Families

Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries

Toward an international consensus—Integrating lipoprotein apheresis and new lipid-lowering drugs

Analysis of LDLR mutations in familial hypercholesterolemia patients in Greece by use of the NanoChip® Microelectronic Array Technology

Novel LDLR Variants in Patients with Familial Hypercholesterolemia: In Silico Analysis as a Tool to Predict Pathogenic Variants in Children and Their Families: In Silico Analysis of Novel LDLR Variants

POR28 SNP is associated with lipid response to atorvastatin in children and adolescents with familial hypercholesterolemia

Refinement of variant selection for the LDL-C genetic risk score in the diagnosis of the polygenic form of clinical Familial Hypercholesterolemia and replication in samples from six countries

Development of a universal chemiluminometric genotyping method for high-throughput detection of 7 LDLR gene mutations in greek population

Neutral lipid storage disease—response to dietary intervention

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