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Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetesRecessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis.The muscle-bone interaction in Turner syndrome.Treated Autoimmune Thyroid Disease Is Associated with a Decreased Quality of Life among Young Persons with Type 1 Diabetes.Case report: type 1 diabetes in monozygotic quadruplets.The effect of diabetes-associated autoantigens on cell processes in human PBMCs and their relevance to autoimmune diabetes development.Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetesHarmonize care to optimize outcome in children and adolescents with diabetes mellitus: treatment recommendations in Europe.The incidence of type 1 diabetes in young Czech children stopped rising.Higher maternal age at delivery, and lower birth orders are associated with increased risk of childhood type 1 diabetes mellitus.Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23Androgen production in pediatric adrenocortical tumors may occur via both the classic and/or the alternative backdoor pathway.Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency.Possibilities and challenges of a large international benchmarking in pediatric diabetology-The SWEET experience.The development and implementation of the SWEET Peer Review Programme for pediatric diabetes centres.A Rare Variant of Turner Syndrome in Four Sequential Generations: Effect of the Interplay of Growth Hormone Treatment and Estrogens on Body Proportion.HbA1c but not diabetes duration predicts increased arterial stiffness in adolescents with poorly controlled type 1 diabetes.[Heterogeneity of childhood diabetes and its therapeutic implications].High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.Two cases of diabetic ketoacidosis in HNF1A-MODY linked to severe dehydration: is it time to change the diagnostic criteria for MODY?Healthy first-degree relatives of patients with type 1 diabetes exhibit significant differences in basal gene expression pattern of immunocompetent cells compared to controls: expression pattern as predeterminant of autoimmune diabetes.Protein microarray analysis as a tool for monitoring cellular autoreactivity in type 1 diabetes patients and their relatives.Decreased dendritic cell numbers but increased TLR9-mediated interferon-alpha production in first degree relatives of type 1 diabetes patients.Absence of breast-feeding is associated with the risk of type 1 diabetes: a case-control study in a population with rapidly increasing incidence.[Prediction of insulin-dependent diabetes mellitus in children of first-degree relatives of diabetic patients][Prediction of type 1 diabetes mellitus in first degree Czech relatives of diabetic patients]NEUROD polymorphism Ala45Thr is associated with Type 1 diabetes mellitus in Czech children.Effect of pamidronate treatment on vertebral deformity in children with primary osteoporosis. A pilot study using radiographic morphometry.Pregnancy in a woman suffering from type 1 diabetes associated with Addison's disease and Hashimoto's thyroiditis (fully developed Autoimmune Polyglandular Syndrome Type 2).Continuing increase in incidence of childhood-onset type 1 diabetes in the Czech Republic 1990-2001.Local body composition is associated with gender differences of bone development at the forearm in puberty.Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius.Prepubertal girls with Turner syndrome and children with isolated SHOX deficiency have similar bone geometry at the radius.A 6-Year Follow-Up of Fracture Incidence and Volumetric Bone Mineral Density Development in Girls with Turner Syndrome.Muscle functions and bone strength are impaired in adolescents with type 1 diabetes.The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitus.Effectiveness of SmartGuard Technology in the Prevention of Nocturnal Hypoglycemia After Prolonged Physical Activity.Pediatric diabetes training for healthcare professionals in Europe: Time for change.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.Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?
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onderzoeker
@nl
pediatr, diabetolog
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researcher
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հետազոտող
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name
Z Sumnik
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Z Sumnik
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Zdeněk Šumník
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Zdeněk Šumník
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Zdeněk Šumník
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Z Sumnik
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Z Sumnik
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Zdeněk Šumník
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Zdeněk Šumník
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Zdeněk Šumník
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Sumnik Z
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Zdenek Sumnik
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Z Sumnik
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Z Sumnik
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Zdeněk Šumník
@cs
Zdeněk Šumník
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Zdeněk Šumník
@es
P106
P214
P19
P21
P214
P31
P496
0000-0002-6462-6462
P569
1970-06-14T00:00:00Z
P691
P735
P7859
viaf-85530746