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Stanol ester margarine alone and with simvastatin lowers serum cholesterol in families with familial hypercholesterolemia caused by the FH-North Karelia mutation

Arteriosclerosis, thrombosis, and vascular biology, 2000-02, Vol.20 (2), p.500-506

2000

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White Matter Hyperintensities on T2-Weighted MRI Images among DNA-Verified Older Familial Hypercholesterolemia Patients

Acta radiologica (1987), 2009-04, Vol.50 (3), p.320-326

2009

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Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.3127-3138

1997

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Statin-Treated Familial Hypercholesterolemia Patients with Coronary Heart Disease and Pronounced Atherosclerosis Do Not Have More Brain Lesions than Healthy Controls in Later Middle Age

Acta radiologica (1987), 2007-10, Vol.48 (8), p.894-899

2007

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Neonatal diagnosis of familial hypercholesterolemia in newborns born to a parent with a molecularly defined heterozygous familial hypercholesterolemia

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.3332-3337

1997

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Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men

Forensic science international, 1999-12, Vol.106 (2), p.87-92

1999

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Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample

Forensic science international, 1999-12, Vol.106 (2), p.71-75

1999

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A novel point mutation (Pro84 ← Ser) of the low density lipoprotein receptor gene in a family with moderate hypercholesterolemia

Clinical genetics, 1997-03, Vol.51 (3), p.191-195

1997

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Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses:a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia

Molecular and cellular probes, 1999-12, Vol.13 (6), p.421-424

1999

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A Mutation in the Amino-Terminal End of the Triple Helix of Type II Collagen Causing Severe Osteochondrodysplasia

Genomics (San Diego, Calif.), 1993-04, Vol.16 (1), p.282-285

1993

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Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences

Annals of medicine (Helsinki), 2001, Vol.33 (6), p.410-421

2001

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Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems

Biochemical and biophysical research communications, 1990-07, Vol.170 (2), p.616-620

1990

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Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low‐density‐lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment

Journal of internal medicine, 1995-01, Vol.237 (1), p.43-48

1995

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Cryptosporidium in Asymptomatic Children

Reviews of infectious diseases, 1991-03, Vol.13 (2), p.261-264

1991

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Familial hypercholesterolemia patients treated with statins at no increased risk for intracranial vascular lesions despite increased cholesterol burden and extracranial atherosclerosis

Stroke (1970), 2005-07, Vol.36 (7), p.1572-1574

2005

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Deletions of the low density lipoprotein receptor gene underlying familial hypercholesterolaemia: screening by polymerase chain reaction using pooled DNA and blood samples

Molecular and cellular probes, 1997-02, Vol.11 (1), p.65-70

1997

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Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences. Finnish FH-group

Annals of medicine (Helsinki), 2001-09, Vol.33 (6), p.410-421

2001

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Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low‐density‐lipoprotein receptor gene and Pvu II polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment

Journal of internal medicine, 1995-01, Vol.237 (1), p.43-48

1995

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Heterozygous familial hypercholesterolaemia : the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allene on serum lipid levels and response to lovastatin treatment

Journal of internal medicine, 1995, Vol.237 (1), p.43-48

1995

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Cholesterol metabolism in normal and heterozygous familial hypercholesterolemic newborns

The Journal of laboratory and clinical medicine, 2002-07, Vol.140 (1), p.35-42

2002

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Familial hypercholesterolemia and elevated lipoprotein(a): double heritable risk and new therapeutic opportunities

Journal of internal medicine, 2020-01, Vol.287 (1), p.2-18

2020

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Familial hypercholesterolaemia and COVID‐19: triggering of increased sustained cardiovascular risk

Journal of internal medicine, 2020-06, Vol.287 (6), p.746-747

2020

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Lipoprotein(a) as a risk factor for calcific aortic valvulopathy in heterozygous familial hypercholesterolemia

Atherosclerosis, 2019-02, Vol.281, p.25-30

2019

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Depicting new pharmacological strategies for familial hypercholesterolaemia involving lipoprotein (a)

European heart journal, 2017-12, Vol.38 (48), p.3555-3559

2017

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Stanol ester margarine alone and with simvastatin lowers serum cholesterol in families with familial hypercholesterolemia caused by the FH-North Karelia mutation

White Matter Hyperintensities on T2-Weighted MRI Images among DNA-Verified Older Familial Hypercholesterolemia Patients

Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study

Statin-Treated Familial Hypercholesterolemia Patients with Coronary Heart Disease and Pronounced Atherosclerosis Do Not Have More Brain Lesions than Healthy Controls in Later Middle Age

Neonatal diagnosis of familial hypercholesterolemia in newborns born to a parent with a molecularly defined heterozygous familial hypercholesterolemia

Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men

Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample

A novel point mutation (Pro84 ← Ser) of the low density lipoprotein receptor gene in a family with moderate hypercholesterolemia

Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses:a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia

A Mutation in the Amino-Terminal End of the Triple Helix of Type II Collagen Causing Severe Osteochondrodysplasia

Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences

Amplification of the hypervariable region close to the apolipoprotein B gene: Application to forensic problems

Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low‐density‐lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment

Cryptosporidium in Asymptomatic Children

Familial hypercholesterolemia patients treated with statins at no increased risk for intracranial vascular lesions despite increased cholesterol burden and extracranial atherosclerosis

Deletions of the low density lipoprotein receptor gene underlying familial hypercholesterolaemia: screening by polymerase chain reaction using pooled DNA and blood samples

Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences. Finnish FH-group

Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low‐density‐lipoprotein receptor gene and Pvu II polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment

Heterozygous familial hypercholesterolaemia : the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allene on serum lipid levels and response to lovastatin treatment

Cholesterol metabolism in normal and heterozygous familial hypercholesterolemic newborns

Familial hypercholesterolemia and elevated lipoprotein(a): double heritable risk and new therapeutic opportunities

Familial hypercholesterolaemia and COVID‐19: triggering of increased sustained cardiovascular risk

Lipoprotein(a) as a risk factor for calcific aortic valvulopathy in heterozygous familial hypercholesterolemia

Depicting new pharmacological strategies for familial hypercholesterolaemia involving lipoprotein (a)

Roadmap for a precision-medicine initiative in the Nordic region

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