Výsledky vyhledávání - "Clemens Schliesser"

Autosomal Recessive Hypercholesterolemia in Three Sisters with Phenotypic Homozygous Familial Hypercholesterolemia: Diagnostic and Therapeutic Procedures

Autor: Kenneth R. Wilund, Anja Vogt, E. Steinhagen-Thiessen, Clemens Schliesser, Hans-Peter Thomas, Ursula Kassner

Publikováno v: Therapeutic Apheresis and Dialysis. 8:275-280

Familial hypercholesterolemia is an autosomal-dominant inherited disorder caused by mutations in the low-density lipoprotein (LDL) receptor gene. The homozygous form is characterized by high-serum LDL cholesterol concentrations, xanthoma formation an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcfee35f875190febcf6efb0ed0bb01a
https://doi.org/10.1111/j.1526-0968.2004.00143.x

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Akademický článek

Autosomal Recessive Hypercholesterolemia in Three Sisters with Phenotypic Homozygous Familial Hypercholesterolemia Diagnostic and Therapeutic Procedures.

Autor: Thomas, Hans-Peter, Vogt, Anja, Wilund, Kenneth R., Schliesser, Clemens, Steinhagen-Thiessen, Elisabeth, Kassner, Ursula

Publikováno v: Therapeutic Apheresis & Dialysis; Aug2004, Vol. 8 Issue 4, p275-280, 6p, 2 Color Photographs, 1 Chart, 1 Graph

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