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Enhanced STAT3 phosphorylation and PD-L1 expression in myeloid dendritic cells indicate impaired IL-27Ralpha signaling in type 1 diabetes

Scientific reports, 2020-01, Vol.10 (1), p.493-493, Article 493

2020

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Introduction of continuous glucose monitoring (CGM) is a key factor in decreasing HbA1c in war refugee children with type 1 diabetes

Diabetes research and clinical practice, 2024-02, Vol.208, p.111118-111118, Article 111118

2024

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Intralymphatic GAD-Alum (Diamyd®) Improves Glycemic Control in Type 1 Diabetes With HLA DR3-DQ2

The journal of clinical endocrinology and metabolism, 2022-09, Vol.107 (9), p.2644-2651

2022

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Artificially low cortical bone mineral density in Turner syndrome is due to the partial volume effect

Osteoporosis international, 2015-03, Vol.26 (3), p.1213-1218

2015

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The current landscape of European registries for rare endocrine conditions

European journal of endocrinology, 2019-01, Vol.180 (1), p.89

2019

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Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme

Diabetic medicine, 2016-12, Vol.33 (12), p.1712-1716

2016

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Electronic reporting of rare endocrine conditions within a clinical network: results from the EuRRECa project

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

2023

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The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitus

Diabetic medicine, 2014-02, Vol.31 (2), p.165-171

2014

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Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

The journal of clinical endocrinology and metabolism, 2013-07, Vol.98 (7), p.E1241-E1247

2013

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Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-03, Vol.18 (2), p.222-228

2012

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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

Scandinavian journal of immunology, 2012-02, Vol.75 (2), p.210-219

2012

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Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α

Diabetologia, 2003-02, Vol.46 (2), p.291-295

2003

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Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency

Experimental and clinical endocrinology & diabetes, 2013-02, Vol.121 (2), p.109

2013

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Sulphonylurea treatment does not improve psychomotor development in children with KCNJ11 mutations causing permanent neonatal diabetes mellitus accompanied by developmental delay and epilepsy (DEND syndrome)

Diabetic medicine, 2007-10, Vol.24 (10), p.1176-1178

2007

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Bone mineral density is low even in prepubertal girls with Turner syndrome: A pQCT study

Bone (New York, N.Y.), 2009-07, Vol.45, p.S77-S78

2009

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Low-carbohydrate diet in children and young people with type 1 diabetes: A randomized controlled trial with cross-over design

Diabetes research and clinical practice, 2024-09, p.111844, Article 111844

2024

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Incidence trends for childhood type 1 diabetes in Europe during 1989–2003 and predicted new cases 2005–20: a multicentre prospective registration study

The Lancet (British edition), 2009-06, Vol.373 (9680), p.2027-2033

2009

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Thyroid autoimmunity in children with coexisting type 1 diabetes mellitus and celiac disease: a multicenter study

Journal of pediatric endocrinology & metabolism : JPEM, 2006-04, Vol.19 (4), p.517

2006

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Persistent heterogeneity in diabetes technology reimbursement for children with type 1 diabetes: The SWEET perspective

Pediatric diabetes, 2019-06, Vol.20 (4), p.434-443

2019

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Reference data for jumping mechanography in healthy children and adolescents aged 6-18 years

Journal of musculoskeletal & neuronal interactions, 2013-09, Vol.13 (3), p.297-311

2013

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Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes

The New England journal of medicine, 2004-04, Vol.350 (18), p.1838-1849

2004

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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)

Experimental and clinical endocrinology & diabetes, 2004-06, Vol.112 (6), p.333

2004

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Enhanced STAT3 phosphorylation and PD-L1 expression in myeloid dendritic cells indicate impaired IL-27Ralpha signaling in type 1 diabetes

Introduction of continuous glucose monitoring (CGM) is a key factor in decreasing HbA1c in war refugee children with type 1 diabetes

Intralymphatic GAD-Alum (Diamyd®) Improves Glycemic Control in Type 1 Diabetes With HLA DR3-DQ2

Artificially low cortical bone mineral density in Turner syndrome is due to the partial volume effect

The current landscape of European registries for rare endocrine conditions

Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme

Electronic reporting of rare endocrine conditions within a clinical network: results from the EuRRECa project

The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitus

Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius

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

Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α

Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency

Temporal trends in diabetic ketoacidosis at diagnosis of paediatric type 1 diabetes between 2006 and 2016: results from 13 countries in three continents

Sulphonylurea treatment does not improve psychomotor development in children with KCNJ11 mutations causing permanent neonatal diabetes mellitus accompanied by developmental delay and epilepsy (DEND syndrome)

Bone mineral density is low even in prepubertal girls with Turner syndrome: A pQCT study

Low-carbohydrate diet in children and young people with type 1 diabetes: A randomized controlled trial with cross-over design

Intralymphatic Glutamic Acid Decarboxylase With Vitamin D Supplementation in Recent-Onset Type 1 Diabetes: A Double-Blind, Randomized, Placebo-Controlled Phase IIb Trial

Incidence trends for childhood type 1 diabetes in Europe during 1989–2003 and predicted new cases 2005–20: a multicentre prospective registration study

Impact of the COVID-19 pandemic on long-term trends in the prevalence of diabetic ketoacidosis at diagnosis of paediatric type 1 diabetes: an international multicentre study based on data from 13 national diabetes registries

Thyroid autoimmunity in children with coexisting type 1 diabetes mellitus and celiac disease: a multicenter study

Persistent heterogeneity in diabetes technology reimbursement for children with type 1 diabetes: The SWEET perspective

Reference data for jumping mechanography in healthy children and adolescents aged 6-18 years

Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes

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)

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