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Akademický článek

Compliance of the aorta in two diseases affecting vascular elasticity, familial hypercholesterolemia and diabetes: a MRI study

Autor: Sami Soljanlahti, Taina Autti, Laura Hyttinen, Alpo F Vuorio, Pekka Keto, Kirsi Lauerma

Publikováno v: Vascular Health and Risk Management, Vol Volume 4, Pp 1103-1109 (2008)

Sami Soljanlahti1, Taina Autti1, Laura Hyttinen2, Alpo F Vuorio3, Pekka Keto1, Kirsi Lauerma11Helsinki Medical Imaging Center, Helsinki University Central Hospital, Helsinki, Finland; 2Department of Internal Medicine, North Karelia Central Hospital,

Externí odkaz: https://doaj.org/article/f477d2f3bf15474f954469cd211c0cd3

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Akademický článek

Aorta of young and middle-aged heterozygous familial hypercholesterolemia patients shows no functional or morphological impairment assessed by MRI

Autor: Sami Soljanlahti, Taina Autti, Alpo F Vuorio, Pekka Keto, Hannu Turtola, Kirsi Lauerma

Publikováno v: Vascular Health and Risk Management, Vol Volume 4, Pp 923-929 (2008)

Sami Soljanlahti1, Taina Autti1, Alpo F Vuorio2, Pekka Keto1, Hannu Turtola3, Kirsi Lauerma11Helsinki Medical Imaging Center, Helsinki University Central Hospital, Helsinki, Finland; 2Division of Internal Medicine, Department of Medicine, University

Externí odkaz: https://doaj.org/article/62aa8f9f63854e2789fe6f4c2b7bc3ea

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Hypolipidemic treatment of heterozygous familial hypercholesterolemia: a lifelong challenge

Autor: Petri T. Kovanen, Alpo F Vuorio, Helena Gylling

Publikováno v: Expert review of cardiovascular therapy. 2(3)

In familial hypercholesterolemia, a defect in low-density lipoprotein receptors causes lifelong two- to threefold elevations in serum low-density lipoprotein-cholesterol levels. This leads to early atherosclerotic changes in infancy. Lifelong hypolip

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48d09d12eb0d6ad47a10dc36fb5fe32f
https://pubmed.ncbi.nlm.nih.gov/15151486

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

Autor: A F, Vuorio, K, Aalto-Setälä, U M, Koivisto, H, Turtola, H, Nissen, P T, Kovanen, T A, Miettinen, H, Gylling, H, Oksanen, K, Kontula

Publikováno v: Annals of medicine. 33(6)

Familial hypercholesterolaemia (FH) is an autosomal co-dominantly inherited condition resulting from mutations of the low-density lipoprotein (LDL) receptor which occur in heterozygous form in approximately one in 500 individuals. Clinically, FH is c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1338459d4994135640e0d55afaeae524
https://pubmed.ncbi.nlm.nih.gov/11585102

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