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Myeloid - derived suppressor cells in Type 1 diabetes are an expanded population exhibiting diverse T-cell suppressor mechanisms

PloS one, 2020-11, Vol.15 (11), p.e0242092-e0242092

2020

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Tolerogenic Dendritic Cells from Poorly Compensated Type 1 Diabetes Patients Have Decreased Ability To Induce Stable Antigen-Specific T Cell Hyporesponsiveness and Generation of Suppressive Regulatory T Cells

The Journal of immunology (1950), 2017-01, Vol.198 (2), p.729-740

2017

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Glycemic Control by Treatment Modalities: National Registry-Based Population Data in Children and Adolescents with Type 1 Diabetes

Hormone research in paediatrics, 2024, Vol.97 (1), p.70-79

2024

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Can auscultatory blood pressure normative values be used for evaluation of oscillometric blood pressure in children?

The journal of clinical hypertension (Greenwich, Conn.), 2017-04, Vol.19 (4), p.381-387

2017

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Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency

International archives of allergy and immunology, 2016-03, Vol.168 (3), p.197-204

2016

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Current procedures in diagnosis, treatment and prevention of cow's milk protein allergy (CMPA)

Československá pediatrie, 2024-08, Vol.79 (4), p.191-194

2024

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Brief resolved unexplained event (BRUE)

Československá pediatrie, 2023-12, Vol.78 (6), p.295-297

2023

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The importance of pulse wave velocity measurement in paediatric population with an increased risk of cardiovascular diseases – Type 1 diabetes and chronic kidney disease

Cor et vasa (English ed.), 2016-12, Vol.58 (6), p.e623-e630

2016

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Eosinophils from patients with type 1 diabetes mellitus express high level of myeloid alpha-defensins and myeloperoxidase

Cellular immunology, 2012, Vol.273 (2), p.158-163

2012

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Muscle functions and bone strength are impaired in adolescents with type 1 diabetes

Bone (New York, N.Y.), 2018-01, Vol.106, p.22-27

2018

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Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

Journal of human genetics, 2017-08, Vol.62 (8), p.755-762

2017

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HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes

Journal of Pediatric Endocrinology and Metabolism, 2011-06, Vol.24 (5-6), p.377-379

2011

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Low-Carbohydrate Diet among Children with Type 1 Diabetes: A Multi-Center Study

Nutrients, 2021-10, Vol.13 (11), p.3903

2021

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Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Frontiers in endocrinology (Lausanne), 2023-01, Vol.13, p.1102968-1102968

2023

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Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based study

Frontiers in endocrinology (Lausanne), 2023-10, Vol.14, p.1283181-1283181

2023

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Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene

Endocrine Connections, 2024-10, Vol.13 (10), p.1-8

2024

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Novel calcium-sensing receptor cytoplasmic tail deletion mutation causing autosomal dominant hypocalcemia: molecular and clinical study

European journal of endocrinology, 2016-04, Vol.174 (4), p.K1-K11

2016

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Analysis of children with familial short stature: who should be indicated for genetic testing?

Endocrine Connections, 2023-10, Vol.12 (10), p.1-8

2023

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The implementation of modern technology into standard of care of type 1 diabetes

Československá pediatrie, 2022-03, Vol.77 (2), p.78-85

2022

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Five years of improving diabetes control in Czech children after the establishment of the population‐based childhood diabetes register ČENDA

Pediatric diabetes, 2020-02, Vol.21 (1), p.77-87

2020

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The expansion of national newborn screening marks an advancement in diagnosing patients with severe inborn errors of immunity

Československá pediatrie, 2024-05, Vol.79 (3), p.136-141

2024

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Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

BMC medical genetics, 2010-03, Vol.11 (1), p.42-42

2010

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Myeloid - derived suppressor cells in Type 1 diabetes are an expanded population exhibiting diverse T-cell suppressor mechanisms

PloS one, 2020-01, Vol.15 (11)

2020

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Myeloid - derived suppressor cells in Type 1 diabetes are an expanded population exhibiting diverse T-cell suppressor mechanisms

Tolerogenic Dendritic Cells from Poorly Compensated Type 1 Diabetes Patients Have Decreased Ability To Induce Stable Antigen-Specific T Cell Hyporesponsiveness and Generation of Suppressive Regulatory T Cells

Glycemic Control by Treatment Modalities: National Registry-Based Population Data in Children and Adolescents with Type 1 Diabetes

Can auscultatory blood pressure normative values be used for evaluation of oscillometric blood pressure in children?

Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency

Current procedures in diagnosis, treatment and prevention of cow's milk protein allergy (CMPA)

Brief resolved unexplained event (BRUE)

The importance of pulse wave velocity measurement in paediatric population with an increased risk of cardiovascular diseases – Type 1 diabetes and chronic kidney disease

Eosinophils from patients with type 1 diabetes mellitus express high level of myeloid alpha-defensins and myeloperoxidase

Muscle functions and bone strength are impaired in adolescents with type 1 diabetes

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes

Low-Carbohydrate Diet among Children with Type 1 Diabetes: A Multi-Center Study

Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based study

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene

Novel calcium-sensing receptor cytoplasmic tail deletion mutation causing autosomal dominant hypocalcemia: molecular and clinical study

Analysis of children with familial short stature: who should be indicated for genetic testing?

The implementation of modern technology into standard of care of type 1 diabetes

Pubertal growth in children born small for gestational age (SGA) with persistent short stature (SGA-SS). Growth hormone treatment outcomes from data of the Czech countywide REPAR database

Adult height in children born small for gestational age (SGA) with persistent short stature (SGA-SS). Growth hormone treatment outcomes from data of the Czech countrywide REPAR database

Five years of improving diabetes control in Czech children after the establishment of the population‐based childhood diabetes register ČENDA

The expansion of national newborn screening marks an advancement in diagnosing patients with severe inborn errors of immunity

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

Myeloid - derived suppressor cells in Type 1 diabetes are an expanded population exhibiting diverse T-cell suppressor mechanisms

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