Lista de obras -

A novel mutation (Cys308Phe) of the LDL receptor gene in families from the South-Eastern part of Poland

artículo científico publicado en 2011

A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population

scientific article published on 01 February 2003

Arterial wave velocity and coronary risk factors in patients with type-2 diabetes

artículo científico publicado en 2005

Carotid Plaques Correlates in Patients With Familial Hypercholesterolemia

artículo científico publicado en 2015

Carotid artery plaques - Are risk factors the same in men and women with familial hypercholesterolemia?

artículo científico publicado en 2017

Correlates of pentraxin 3 serum concentration in men and women with type 2 diabetes

artículo científico publicado en 2019

Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency

artículo científico publicado en 2011

Determinants of nonalcoholic fatty liver disease in men and women with type 2 diabetes

artículo científico publicado en 2014

Erratum to: A novel mutation (Cys308Phe) of the LDL receptor gene in families from the South-Eastern part of Poland

artículo científico publicado en 2015

Familial lecithin-cholesterol acyltransferase deficiency: biochemical characteristics and molecular analysis of a new LCAT mutation in a Polish family

artículo científico publicado en 2005

GTP cyclohydrolase I gene polymorphisms are associated with endothelial dysfunction and oxidative stress in patients with type 2 diabetes mellitus

artículo científico publicado en 2014

Intima-media thickness correlates with features of metabolic syndrome in young people with a clinical diagnosis of familial hypercholesterolaemia

artículo científico publicado en 2013

Is now the time for probiotics in diabetes management?

Nonalcoholic fatty liver disease is associated with low HDL cholesterol and coronary angioplasty in patients with type 2 diabetes

artículo científico publicado en 2013

Osteoprotegerin is associated with markers of atherosclerosis and body fat mass in type 2 diabetes patients

artículo científico publicado en 2011

Pentraxin 3 in patients with type 2 diabetes and nonalcoholic fatty liver disease: a promising treatment target for glucagon-like peptide-1 receptor agonists. Authors' reply

artículo científico publicado en 2019

Plasma Asymmetric Dimethylarginine (ADMA) Is Associated With Retinopathy in Type 2 Diabetes

scientific article published on 17 August 2007

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

artículo científico publicado en 2014

Serum pentraxin 3 concentration in patients with type 2 diabetes and nonalcoholic fatty liver disease

artículo científico publicado en 2019

The genetic spectrum of familial hypercholesterolemia in south-eastern Poland

artículo científico publicado en 2015

[Autosomal dominant hypercholesterolemia - underrecognised diagnostic and clinical problem]

scientific article published on 01 September 2009

Lista de obras de

A novel mutation (Cys308Phe) of the LDL receptor gene in families from the South-Eastern part of Poland

A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population

Arterial wave velocity and coronary risk factors in patients with type-2 diabetes

Carotid Plaques Correlates in Patients With Familial Hypercholesterolemia

Carotid artery plaques - Are risk factors the same in men and women with familial hypercholesterolemia?

Correlates of pentraxin 3 serum concentration in men and women with type 2 diabetes

Corticosteroid treatment of kidney disease in a patient with familial lecithin-cholesterol acyltransferase deficiency

Determinants of nonalcoholic fatty liver disease in men and women with type 2 diabetes

Erratum to: A novel mutation (Cys308Phe) of the LDL receptor gene in families from the South-Eastern part of Poland

Familial lecithin-cholesterol acyltransferase deficiency: biochemical characteristics and molecular analysis of a new LCAT mutation in a Polish family

GTP cyclohydrolase I gene polymorphisms are associated with endothelial dysfunction and oxidative stress in patients with type 2 diabetes mellitus

Intima-media thickness correlates with features of metabolic syndrome in young people with a clinical diagnosis of familial hypercholesterolaemia

Is now the time for probiotics in diabetes management?

Nonalcoholic fatty liver disease is associated with low HDL cholesterol and coronary angioplasty in patients with type 2 diabetes

Osteoprotegerin is associated with markers of atherosclerosis and body fat mass in type 2 diabetes patients

Pentraxin 3 in patients with type 2 diabetes and nonalcoholic fatty liver disease: a promising treatment target for glucagon-like peptide-1 receptor agonists. Authors' reply

Plasma Asymmetric Dimethylarginine (ADMA) Is Associated With Retinopathy in Type 2 Diabetes

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

Serum pentraxin 3 concentration in patients with type 2 diabetes and nonalcoholic fatty liver disease

The genetic spectrum of familial hypercholesterolemia in south-eastern Poland

[Autosomal dominant hypercholesterolemia - underrecognised diagnostic and clinical problem]