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Novel insights into genetics and clinics of the HNF1A-MODY

Endocrine regulations (Bratislava), 2019-04, Vol.53 (2), p.110-134

2019

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Complete remission in children and adolescents with type 1 diabetes mellitus-prevalence and factors

Scientific reports, 2023-04, Vol.13 (1), p.6790-6790, Article 6790

2023

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Testosterone imbalance may link depression and increased body weight in premenopausal women

Translational psychiatry, 2019-06, Vol.9 (1), p.160, Article 160

2019

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Concordance of bioactive vs. total immunoreactive serum leptin levels in children with severe early onset obesity

PloS one, 2017-05, Vol.12 (5), p.e0178107-e0178107

2017

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Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same KCNJ11 variants

Endocrine regulations (Bratislava), 2020-10, Vol.54 (4), p.260-265

2020

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Risk factors of post-surgery complications in children with thyroid cancer

International journal of pediatric otorhinolaryngology, 2019-12, Vol.127, p.109673-109673, Article 109673

2019

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Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values

EClinicalMedicine, 2021-07, Vol.37, p.100977-100977, Article 100977

2021

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Associations Between Anxiety, Body Mass Index, and Sex Hormones in Women

Frontiers in psychiatry, 2019-07, Vol.10, p.479-479

2019

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Associations of GHR, IGF-1 and IGFBP-3 expression in adipose tissue cells with obesity-related alterations in corresponding circulating levels and adipose tissue function in children

Adipocyte, 2022-12, Vol.11 (1), p.630-642

2022

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Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents

PloS one, 2017-05, Vol.12 (5), p.e0177222-e0177222

2017

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Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism

Molecular metabolism (Germany), 2017-03, Vol.6 (3), p.295-305

2017

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Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients

Endocrine regulations (Bratislava), 2018-04, Vol.52 (2), p.110-118

2018

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Identification of a Novel β-Cell Glucokinase (GCK) Promoter Mutation (−71G>C) That Modulates GCK Gene Expression Through Loss of Allele-Specific Sp1 Binding Causing Mild Fasting Hyperglycemia in Humans

Diabetes (New York, N.Y.), 2009-08, Vol.58 (8), p.1929-1935

2009

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Thyroid hormone levels and BMI-SDS changes in adolescents with obesity

Frontiers in endocrinology (Lausanne), 2023-12, Vol.14, p.1304970-1304970

2023

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An alternative approach using hs-CRP levels and age of onset in diagnostics of HNF1A-MODY

Diabetic medicine, 2024-05, Vol.41 (5), p.e15265-e15265

2024

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Food preferences and thyroid hormones in children and adolescents with obesity

Frontiers in psychiatry, 2022-07, Vol.13, p.962949-962949

2022

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Genetic testing is necessary for correct diagnosis and treatment in patients with isolated methylmalonic aciduria: a case report

BMC pediatrics, 2021-12, Vol.21 (1), p.578-578, Article 578

2021

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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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The Bright Side of Skin Autofluorescence Determination in Children and Adolescents with Newly Diagnosed Type 1 Diabetes Mellitus: A Potential Predictor of Remission?

International journal of environmental research and public health, 2022-09, Vol.19 (19), p.11950

2022

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De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed

Diabetologia, 2014-03, Vol.57 (3), p.480-484

2014

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The Bone Markers Sclerostin, Osteoprotegerin, and Bone-Specific Alkaline Phosphatase Are Related to Insulin Resistance in Children and Adolescents, Independent of Their Association with Growth and Obesity

Hormone research in paediatrics, 2019-01, Vol.91 (1), p.1-8

2019

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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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Severe Insulin Resistance and Intrauterine Growth Deficiency Associated With Haploinsufficiency for INSR and CHN2

Diabetes (New York, N.Y.), 2009-12, Vol.58 (12), p.2954-2961

2009

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Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes

Diabetes care, 2021-01, Vol.44 (1), p.35-42

2021

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Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

The lancet. Diabetes & endocrinology, 2018-08, Vol.6 (8), p.637-646

2018

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Novel insights into genetics and clinics of the HNF1A-MODY

Complete remission in children and adolescents with type 1 diabetes mellitus-prevalence and factors

Testosterone imbalance may link depression and increased body weight in premenopausal women

Concordance of bioactive vs. total immunoreactive serum leptin levels in children with severe early onset obesity

Comparison of diabetes phenotype in children and their mothers with permanent neonatal diabetes mellitus carrying the same KCNJ11 variants

Risk factors of post-surgery complications in children with thyroid cancer

Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values

Associations Between Anxiety, Body Mass Index, and Sex Hormones in Women

Associations of GHR, IGF-1 and IGFBP-3 expression in adipose tissue cells with obesity-related alterations in corresponding circulating levels and adipose tissue function in children

Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents

Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism

Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients

Identification of a Novel β-Cell Glucokinase (GCK) Promoter Mutation (−71G>C) That Modulates GCK Gene Expression Through Loss of Allele-Specific Sp1 Binding Causing Mild Fasting Hyperglycemia in Humans

Thyroid hormone levels and BMI-SDS changes in adolescents with obesity

An alternative approach using hs-CRP levels and age of onset in diagnostics of HNF1A-MODY

Food preferences and thyroid hormones in children and adolescents with obesity

Genetic testing is necessary for correct diagnosis and treatment in patients with isolated methylmalonic aciduria: a case report

Clinical implications of the glucokinase impaired function - GCK MODY today

The Bright Side of Skin Autofluorescence Determination in Children and Adolescents with Newly Diagnosed Type 1 Diabetes Mellitus: A Potential Predictor of Remission?

De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed

The Bone Markers Sclerostin, Osteoprotegerin, and Bone-Specific Alkaline Phosphatase Are Related to Insulin Resistance in Children and Adolescents, Independent of Their Association with Growth and Obesity

Immunologic phenotype of a child with the MEHMO syndrome

Severe Insulin Resistance and Intrauterine Growth Deficiency Associated With Haploinsufficiency for INSR and CHN2

Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes

Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

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