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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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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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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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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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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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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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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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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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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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Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report

Endocrine regulations (Bratislava), 2012-04, Vol.46 (2), p.99-105

2012

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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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Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies

Endocrine regulations (Bratislava), 2012-07, Vol.46 (3), p.167-186

2012

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P02-54 Prediabetes in adult growth hormone deficiency is associated with a substantial reduction in serum and adipose tissue expression levels of zinc-α2-glycoprotein

Growth hormone & IGF research, 2012-10, Vol.22, p.S70-S70

2012

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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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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1034

2008

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Sulfonylurea vs insulin therapy in individuals with sulfonylurea‐sensitive permanent neonatal diabetes mellitus, attributable to a KCNJ 11 mutation, and poor glycaemic control

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

2018

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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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Mapping of genetic loci predisposing to hypertriglyceridaemia in the hereditary hypertriglyceridaemic rat: analysis of genetic association with related traits of the insulin resistance syndrome

Diabetologia, 2003-03, Vol.46 (3), p.352-358

2003

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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

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

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

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

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

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

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

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

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

Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report

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

Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies

P02-54 Prediabetes in adult growth hormone deficiency is associated with a substantial reduction in serum and adipose tissue expression levels of zinc-α2-glycoprotein

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

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Sulfonylurea vs insulin therapy in individuals with sulfonylurea‐sensitive permanent neonatal diabetes mellitus, attributable to a KCNJ 11 mutation, and poor glycaemic control

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

Mapping of genetic loci predisposing to hypertriglyceridaemia in the hereditary hypertriglyceridaemic rat: analysis of genetic association with related traits of the insulin resistance syndrome

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