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                            Published/Copyright:
                            
                                October 30, 2025
                            
                        
                    
                
            
  Published Online: 2025-10-30
 
 
  Published in Print: 2025-11-25
 
©2025 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Original Articles
- Spatiotemporal associations between incidence of type 1 diabetes and COVID-19 vaccination rates in children in Germany – a population-based ecological study
- Continuous glucose monitoring evidence of celiac disease in type 1 diabetes
- Impact of race and delayed adoption of diabetes technology on glycemia and partial remission in type 1 diabetes
- Immunogenetic profiling of type 1 diabetes in Jordan: a case-control study on HLA-associated risk and protection
- Annual case counts and clinical characteristics of pediatric and adolescent patients with diabetes in Kenyatta National Hospital, Nairobi, Kenya. A 14 year retrospective study
- Real-world effectiveness of sodium glucose transporter 2 inhibitors among youth with type 2 diabetes
- Investigation of the association between nitric oxide synthase gene variants and NAFLD in adolescents with obesity
- Cardiometabolic outcomes in girls with premature adrenarche: a longitudinal analysis of typical vs. exaggerated presentations
- A disease that is difficult to predict: regional distribution and phenotypic, histopathological and genetic findings in McArdle disease
- Causal analysis of uterine artery pulsatility index-related proteins and the risk of precocious puberty in girls: a Mendelian randomization study
- Case Reports
- Understanding rickets in osteopetrosis via a case: mechanisms and treatment implications
- A case of JAGN1 mutation presenting with atypical diabetes and immunodeficiency
- Compound heterozygous ROBO1 gene variants in a neonate with congenital hypopituitarism, dysmorphic features and midline abnormalities: a case report and review of the literature
- Phenotypic variation among four members in a family with DAX1 deficiency
- MMP13-related metaphyseal dysplasia: a differential diagnosis of rickets
- Congress Abstracts
- JA-PED | Annual Meeting of the German Society for Pediatric and Adolescent Endocrinology and Diabetology (DGPAED e. V.)
Articles in the same Issue
- Frontmatter
- Original Articles
- Spatiotemporal associations between incidence of type 1 diabetes and COVID-19 vaccination rates in children in Germany – a population-based ecological study
- Continuous glucose monitoring evidence of celiac disease in type 1 diabetes
- Impact of race and delayed adoption of diabetes technology on glycemia and partial remission in type 1 diabetes
- Immunogenetic profiling of type 1 diabetes in Jordan: a case-control study on HLA-associated risk and protection
- Annual case counts and clinical characteristics of pediatric and adolescent patients with diabetes in Kenyatta National Hospital, Nairobi, Kenya. A 14 year retrospective study
- Real-world effectiveness of sodium glucose transporter 2 inhibitors among youth with type 2 diabetes
- Investigation of the association between nitric oxide synthase gene variants and NAFLD in adolescents with obesity
- Cardiometabolic outcomes in girls with premature adrenarche: a longitudinal analysis of typical vs. exaggerated presentations
- A disease that is difficult to predict: regional distribution and phenotypic, histopathological and genetic findings in McArdle disease
- Causal analysis of uterine artery pulsatility index-related proteins and the risk of precocious puberty in girls: a Mendelian randomization study
- Case Reports
- Understanding rickets in osteopetrosis via a case: mechanisms and treatment implications
- A case of JAGN1 mutation presenting with atypical diabetes and immunodeficiency
- Compound heterozygous ROBO1 gene variants in a neonate with congenital hypopituitarism, dysmorphic features and midline abnormalities: a case report and review of the literature
- Phenotypic variation among four members in a family with DAX1 deficiency
- MMP13-related metaphyseal dysplasia: a differential diagnosis of rickets
- Congress Abstracts
- JA-PED | Annual Meeting of the German Society for Pediatric and Adolescent Endocrinology and Diabetology (DGPAED e. V.)