Associated Papers
The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
Meshkov A et al.
Genes, 2021
Analysis of lipid metabolism and its impact on the risk of ischemic heart disease in patients with definite familial hypercholesterolemia.
Korneva V et al.
Atherosclerosis. Supplements, 2017
Cholesterol Levels in Genetically Determined Familial Hypercholesterolaemia in Russian Karelia.
Korneva VA et al.
Cholesterol, 2017
[Familial hypercholesterolemia due to a new mutation in the low density lipoprotein receptor gene].
Korneva VA et al.
Klinicheskaia Meditsina, 2014
Familial hypercholesterolemia mutations in Petrozavodsk: no similarity to St. Petersburg mutation spectrum.
Komarova TY et al.
Bmc Medical Genetics, 2013
[New mutations in low-density lipoprotein receptor gene in familial hypercholesterolemia patients from Petrozavodsk].
Komarova TY et al.
Genetika, 2013
[A case of familial hypercholesterolemia caused by a novel mutation p. FsS65:D129X of human low density lipoprotein receptor gene].
Korneva VA et al.
Kardiologiia, 2013
[Clinical signs of homozygous familial hypercholesterolemia].
Malyshev PP et al.
Kardiologiia, 2002
[Current concepts of the pathogenesis of familial hypercholesterolemia].
Khandaker AKh et al.
Kardiologiia, 1988
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