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A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes

Diabetologia, 2011-11, Vol.54 (11), p.2801-2810

2011

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Circulatory and adipose tissue leptin and adiponectin in relationship to resting energy expenditure in patients with chronic obstructive pulmonary disease

Physiological research, 2012-01, Vol.61 (5), p.469-480

2012

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Diabetes treatment in two pregnant women with permanent neonatal diabetes mellitus due to a KCNJ11 mutation

Diabetic medicine, 2020-11, Vol.37 (11), p.1956-1958

2020

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Clinical implications of the glucokinase impaired function - GCK MODY today

Physiological research, 2020, Vol.69 (6), p.995-1011

2020

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Neonatal hypoglycemia, early-onset diabetes and hypopituitarism due to the mutation in EIF2S3 gene causing MEHMO syndrome

Physiological research, 2018-01, Vol.67 (2), p.331-337

2018

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High prevalence of prediabetes and diabetes in a population exposed to high levels of an organochlorine cocktail

Diabetologia, 2010-05, Vol.53 (5), p.899-906

2010

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The molecular genetic background of familial hypercholesterolemia: data from the Slovak nation-wide survey

Physiological research, 2017-01, Vol.66 (1), p.75-84

2017

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Immunologic phenotype of a child with the MEHMO syndrome

Physiological research, 2020-11, Vol.69 (5), p.927-932

2020

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Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications

European archives of oto-rhino-laryngology, 2014-06, Vol.271 (6), p.1401-1407

2014

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Sulfonylurea vs insulin therapy in individuals with sulfonylurea‐sensitive permanent neonatal diabetes mellitus, attributable to a KCNJ11 mutation, and poor glycaemic control

Diabetic medicine, 2018-03, Vol.35 (3), p.386-391

2018

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Mapping of genetic determinants of the sympathoneural response to stress

Physiological genomics, 2005-01, Vol.20 (2), p.183-187

2005

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Molecular analysis of genes involved in lipoprotein lipase deficiency in Slovak patients with familial chylomicronemia

Atherosclerosis, 2016-09, Vol.252, p.e73-e73

2016

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Insulin Resistance in the Hereditary Hypertriglyceridemic Rat Is Associated with an Impairment of Δ-6 Desaturase Expression in Liver

Annals of the New York Academy of Sciences, 2002-06, Vol.967 (1), p.446-453

2002

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Concerted action of leptin in regulation of fatty acid oxidation in skeletal muscle and liver

Experimental and clinical endocrinology & diabetes, 2007-04, Vol.115 (4), p.244-251

2007

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Hereditary bilateral sudden sensorineural hearing loss

Bratislava Medical Journal, 2019, Vol.120 (9), p.699-702

2019

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DNA diagnostics of familial hypercholesterolemia: Slovak experience

Atherosclerosis, 2015-07, Vol.241 (1), p.e114-e114

2015

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Melanocortin-4 receptor gene mutations in obese Slovak children

Physiological research, 2015-01, Vol.64 (6), p.883-890

2015

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Obesogenic and diabetogenic impact of high organochlorine levels (HCB, p,p'-DDE, PCBs) on inhabitants in the highly polluted Eastern Slovakia

Endocrine regulations (Bratislava), 2014-01, Vol.48 (1), p.17-24

2014

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An Increase in Peroxisomal Fatty Acid Oxidation Is Not Sufficient to Prevent Tissue Lipid Accumulation in hHTg Rats

Annals of the New York Academy of Sciences, 2002-06, Vol.967 (1), p.71-79

2002

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Molecular-genetic aspects of familial hypercholesterolemia

Endocrine regulations (Bratislava), 2015-07, Vol.49 (3), p.164-181

2015

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Effects of Hypoxia on Adipose Tissue Expression of NFκB, IκBα, IKKγ and IKAP in Patients with Chronic Obstructive Pulmonary Disease

Cell biochemistry and biophysics, 2013-05, Vol.66 (1), p.7-12

2013

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hypotriglyceridemic effect of dietary n-3 FA is associated with increased beta-oxidation and reduced leptin expression

Lipids, 2003-10, Vol.38 (10), p.1023-1029

2003

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Age of obesity onset in MC4R mutation carriers

Endocrine regulations (Bratislava), 2015-07, Vol.49 (3), p.137-140

2015

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Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitro

Diabetic medicine, 2010-06, Vol.27 (6), p.631-635

2010

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Increased thyroid volume, prevalence of thyroid antibodies and impaired fasting glucose in young adults from organochlorine cocktail polluted area: Outcome of transgenerational transmission?

Chemosphere (Oxford), 2008-10, Vol.73 (7), p.1145-1150

2008

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A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes

Circulatory and adipose tissue leptin and adiponectin in relationship to resting energy expenditure in patients with chronic obstructive pulmonary disease

Diabetes treatment in two pregnant women with permanent neonatal diabetes mellitus due to a KCNJ11 mutation

Clinical implications of the glucokinase impaired function - GCK MODY today

Neonatal hypoglycemia, early-onset diabetes and hypopituitarism due to the mutation in EIF2S3 gene causing MEHMO syndrome

High prevalence of prediabetes and diabetes in a population exposed to high levels of an organochlorine cocktail

The molecular genetic background of familial hypercholesterolemia: data from the Slovak nation-wide survey

Immunologic phenotype of a child with the MEHMO syndrome

Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications

Sulfonylurea vs insulin therapy in individuals with sulfonylurea‐sensitive permanent neonatal diabetes mellitus, attributable to a KCNJ11 mutation, and poor glycaemic control

Mapping of genetic determinants of the sympathoneural response to stress

Molecular analysis of genes involved in lipoprotein lipase deficiency in Slovak patients with familial chylomicronemia

Insulin Resistance in the Hereditary Hypertriglyceridemic Rat Is Associated with an Impairment of Δ-6 Desaturase Expression in Liver

Concerted action of leptin in regulation of fatty acid oxidation in skeletal muscle and liver

Hereditary bilateral sudden sensorineural hearing loss

DNA diagnostics of familial hypercholesterolemia: Slovak experience

Melanocortin-4 receptor gene mutations in obese Slovak children

Obesogenic and diabetogenic impact of high organochlorine levels (HCB, p,p'-DDE, PCBs) on inhabitants in the highly polluted Eastern Slovakia

An Increase in Peroxisomal Fatty Acid Oxidation Is Not Sufficient to Prevent Tissue Lipid Accumulation in hHTg Rats

Molecular-genetic aspects of familial hypercholesterolemia

Effects of Hypoxia on Adipose Tissue Expression of NFκB, IκBα, IKKγ and IKAP in Patients with Chronic Obstructive Pulmonary Disease

hypotriglyceridemic effect of dietary n-3 FA is associated with increased beta-oxidation and reduced leptin expression

Age of obesity onset in MC4R mutation carriers

Novel monogenic diabetes mutations in the P2 promoter of the HNF4A gene are associated with impaired function in vitro

Increased thyroid volume, prevalence of thyroid antibodies and impaired fasting glucose in young adults from organochlorine cocktail polluted area: Outcome of transgenerational transmission?

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