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Publications by H Meinertz

Characteristics of 46 Heterozygous Carriers and 57 Unaffected Relatives in Five Danish Families With Familial Defective Apolipoprotein B-100

Arteriosclerosis and Thrombosis: A Journal of Vascular Biology

1994

English

Related publications

Rapid Diagnosis of Familial Defective Apolipoprotein B-100

Clinical Chemistry and Laboratory Medicine

Biochemistry

Medicine

Clinical Biochemistry

1991

English

Familial Defective Apolipoprotein B-100 in a Group of Hypercholesterolaemic Patients in Poland. Identification of a New Mutation Thr3492Ile in the Apolipoprotein B Gene

European Journal of Human Genetics

Genetics

2001

English

Apolipoprotein E Polymorphism and Heterozygous Familial Hypercholesterolemia. Sex-Specific Effects

Arteriosclerosis and Thrombosis: A Journal of Vascular Biology

1994

English

Familial Expression of Anti-Saccharomyces Cerevisiae Mannan Antibodies in Affected and Unaffected Relatives of Patients With Crohn's Disease

Gut

Gastroenterology

2000

English

Accumulation of "Small Dense" Low Density Lipoproteins (LDL) in a Homozygous Patients With Familial Defective Apolipoprotein B-100 Results From Heterogenous Interaction of LDL Subfractions With the LDL Receptor.

Journal of Clinical Investigation

Medicine

1993

English

Genetic Study of Low-Density Lipoprotein Receptor Gene and Apolipoprotein B-100 Gene Among Malaysian Patients With Familial Hypercholesterolaemia

International Archives of Medicine

2016

English

Analysis of HDL-microRNA Panel in Heterozygous Familial Hypercholesterolemia Subjects With LDL Receptor Null or Defective Mutation

Scientific Reports

Multidisciplinary

2019

English

Clinical and Biochemical Characteristics and Bone Mineral Density of Homozygous, Compound Heterozygous and Heterozygous Carriers of Three novelIGFALSmutations

European Journal of Endocrinology

English

Decreased Production Rates of VLDL Triglycerides and ApoB-100 in Subjects Heterozygous for Familial Hypobetalipoproteinemia

Arteriosclerosis, Thrombosis, and Vascular Biology

Cardiovascular Medicine

Cardiology

1999

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by H Meinertz

Characteristics of 46 Heterozygous Carriers and 57 Unaffected Relatives in Five Danish Families With Familial Defective Apolipoprotein B-100

Related publications

Rapid Diagnosis of Familial Defective Apolipoprotein B-100

Familial Defective Apolipoprotein B-100 in a Group of Hypercholesterolaemic Patients in Poland. Identification of a New Mutation Thr3492Ile in the Apolipoprotein B Gene

Apolipoprotein E Polymorphism and Heterozygous Familial Hypercholesterolemia. Sex-Specific Effects

Familial Expression of Anti-Saccharomyces Cerevisiae Mannan Antibodies in Affected and Unaffected Relatives of Patients With Crohn's Disease

Accumulation of "Small Dense" Low Density Lipoproteins (LDL) in a Homozygous Patients With Familial Defective Apolipoprotein B-100 Results From Heterogenous Interaction of LDL Subfractions With the LDL Receptor.

Genetic Study of Low-Density Lipoprotein Receptor Gene and Apolipoprotein B-100 Gene Among Malaysian Patients With Familial Hypercholesterolaemia

Analysis of HDL-microRNA Panel in Heterozygous Familial Hypercholesterolemia Subjects With LDL Receptor Null or Defective Mutation

Clinical and Biochemical Characteristics and Bone Mineral Density of Homozygous, Compound Heterozygous and Heterozygous Carriers of Three novelIGFALSmutations

Decreased Production Rates of VLDL Triglycerides and ApoB-100 in Subjects Heterozygous for Familial Hypobetalipoproteinemia