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GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

Diabetes (New York, N.Y.), 2013-03, Vol.62 (3), p.993-997

2013

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Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis

The Lancet (British edition), 2010-03, Vol.375 (9719), p.1007-1013

2010

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Cystic fibrosis across Europe: EuroCareCF analysis of demographic data from 35 countries

Journal of cystic fibrosis, 2010-12, Vol.9, p.S5-S21

2010

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No Effect of the Altered Peptide Ligand NBI-6024 on β-Cell Residual Function and Insulin Needs in New-Onset Type 1 Diabetes

Diabetes care, 2009-11, Vol.32 (11), p.2036-2040

2009

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Recommendations for age-appropriate education of children and adolescents with diabetes and their parents in the European Union

Pediatric diabetes, 2012-09, Vol.13 (s16), p.20-28

2012

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Comparison of Two Prognostic Models in Patients with Metastatic Renal Cancer Treated with Sunitinib: a Retrospective, Registry-Based Study

Targeted oncology, 2015-12, Vol.10 (4), p.557-563

2015

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Harmonize care to optimize outcome in children and adolescents with diabetes mellitus: treatment recommendations in Europe

Pediatric diabetes, 2012-09, Vol.13 (s16), p.15-19

2012

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Caesarean section is associated with an increased risk of childhood-onset type 1 diabetes mellitus: a meta-analysis of observational studies

Diabetologia, 2008-05, Vol.51 (5), p.726-735

2008

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Effectiveness of sequencing selected exons of DNAH5 and DNAI1 in diagnosis of primary ciliary dyskinesia

Pediatric pulmonology, 2012-09, Vol.47 (9), p.864-875

2012

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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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Glucokinase Gene May Be a More Suitable Target Than the Insulin Gene for Detection of β Cell Death

Endocrinology (Philadelphia), 2017-07, Vol.158 (7), p.2058-2065

2017

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Nature-derived microbiota exposure as a novel immunomodulatory approach

Future microbiology, 2018-06, Vol.13 (7), p.737-744

2018

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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

2016

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Two Cases of Diabetic Ketoacidosis in HNF1A-MODY Linked to Severe Dehydration: Is it time to change the diagnostic criteria for MODY?

Diabetes care, 2013-09, Vol.36 (9), p.2573-2574

2013

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The bacteriome at the onset of type 1 diabetes: A study from four geographically distant African and Asian countries

Diabetes research and clinical practice, 2018-10, Vol.144, p.51-62

2018

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Quality of Life and Treatment Satisfaction in Participants with Maturity-Onset Diabetes of the Young: A Comparison to Other Major Forms of Diabetes

Experimental and clinical endocrinology & diabetes, 2022-02, Vol.130 (2), p.85

2022

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High Prevalence of PROP1 Defects in Lithuania: Phenotypic Findings in an Ethnically Homogenous Cohort of Patients With Multiple Pituitary Hormone Deficiency

The journal of clinical endocrinology and metabolism, 2014-01, Vol.99 (1), p.299-306

2014

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Bone geometry and volumetric bone mineral density in girls with Turner syndrome of different pubertal stages

Clinical endocrinology (Oxford), 2011-04, Vol.74 (4), p.445-452

2011

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Frameshift mutations in the insulin gene leading to prolonged molecule of insulin in two families with Maturity-Onset Diabetes of the Young

European journal of medical genetics, 2015-04, Vol.58 (4), p.230-234

2015

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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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Direct PCR Detection of Burkholderia cepacia Complex and Identification of Its Genomovars by Using Sputum as Source of DNA

Journal of Clinical Microbiology, 2002-09, Vol.40 (9), p.3485-3488

2002

Volltextzugriff (PDF)

Human Enterovirus RNA in Monthly Fecal Samples and Islet Autoimmunity in Norwegian Children With High Genetic Risk for Type 1 Diabetes: The MIDIA study

Diabetes care, 2011-01, Vol.34 (1), p.151-155

2011

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Lessons from whole-exome sequencing in MODYX families

Diabetes research and clinical practice, 2014-06, Vol.104 (3), p.e72-e74

2014

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No independent role of the −1123 G > C and + 2740 A > G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations

Diabetes research and clinical practice, 2007-05, Vol.76 (2), p.297-303

2007

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Association of single nucleotide polymorphisms within cytokine genes with juvenile idiopathic arthritis in the Czech population

Journal of rheumatology, 2004-06, Vol.31 (6), p.1206

2004

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GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis

Cystic fibrosis across Europe: EuroCareCF analysis of demographic data from 35 countries

No Effect of the Altered Peptide Ligand NBI-6024 on β-Cell Residual Function and Insulin Needs in New-Onset Type 1 Diabetes

Recommendations for age-appropriate education of children and adolescents with diabetes and their parents in the European Union

Comparison of Two Prognostic Models in Patients with Metastatic Renal Cancer Treated with Sunitinib: a Retrospective, Registry-Based Study

Harmonize care to optimize outcome in children and adolescents with diabetes mellitus: treatment recommendations in Europe

Caesarean section is associated with an increased risk of childhood-onset type 1 diabetes mellitus: a meta-analysis of observational studies

Effectiveness of sequencing selected exons of DNAH5 and DNAI1 in diagnosis of primary ciliary dyskinesia

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

Glucokinase Gene May Be a More Suitable Target Than the Insulin Gene for Detection of β Cell Death

Nature-derived microbiota exposure as a novel immunomodulatory approach

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

Two Cases of Diabetic Ketoacidosis in HNF1A-MODY Linked to Severe Dehydration: Is it time to change the diagnostic criteria for MODY?

The bacteriome at the onset of type 1 diabetes: A study from four geographically distant African and Asian countries

Quality of Life and Treatment Satisfaction in Participants with Maturity-Onset Diabetes of the Young: A Comparison to Other Major Forms of Diabetes

High Prevalence of PROP1 Defects in Lithuania: Phenotypic Findings in an Ethnically Homogenous Cohort of Patients With Multiple Pituitary Hormone Deficiency

Bone geometry and volumetric bone mineral density in girls with Turner syndrome of different pubertal stages

Frameshift mutations in the insulin gene leading to prolonged molecule of insulin in two families with Maturity-Onset Diabetes of the Young

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

Direct PCR Detection of Burkholderia cepacia Complex and Identification of Its Genomovars by Using Sputum as Source of DNA

Human Enterovirus RNA in Monthly Fecal Samples and Islet Autoimmunity in Norwegian Children With High Genetic Risk for Type 1 Diabetes: The MIDIA study

Lessons from whole-exome sequencing in MODYX families

No independent role of the −1123 G > C and + 2740 A > G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations

Association of single nucleotide polymorphisms within cytokine genes with juvenile idiopathic arthritis in the Czech population

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