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Publicly Available Published by De Gruyter January 17, 2022

Frontmatter

From the journal Journal of Pediatric Endocrinology and Metabolism
https://doi.org/10.1515/jpem-2022-frontmatter1
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Published Online: 2022-01-17
Published in Print: 2022-01-27

©2022 Walter de Gruyter GmbH, Berlin/Boston

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From the journal
Journal of Pediatric Endocrinology and Metabolism
Journal of Pediatric Endocrinology and Metabolism
Volume 35 Issue 1
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Journal and Issue

Articles in the same Issue

Frontmatter
Review Article
Medullary thyroid carcinoma in children: current state of the art and future perspectives
Original Articles
Newly defined peroxisomal disease with novel ACBD5 mutation
Pediatric adrenocortical tumors cohort characteristics and long-term follow-up at a single Argentinian tertiary center
Sleep disorder and behavior problems in children with type 1 diabetes mellitus
Increased hepcidin levels and non-alcoholic fatty liver disease in obese prepubertal children: a further piece to the complex puzzle of metabolic derangements
Screening for testicular adrenal rest tumors among children with congenital adrenal hyperplasia at King Fahad Medical City, Saudi Arabia
The association between vitamin D levels and metabolic syndrome components among metropolitan adolescent population
Utility of wrist circumference in recognition of metabolic syndrome in overweight and obese South Indian children and adolescents
Ketoacidosis in new-onset type 1 diabetes: did the severity increase during the COVID-19 pandemic?
Predictors of decreased bone mineral density in childhood systemic lupus erythematosus: possible role of osteoprotegerin gene polymorphisms
Psychiatric behavioral effect and characteristics of type 2 diabetes mellitus on Japanese patients with Prader-Willi syndrome: a preliminary retrospective study
Biochemical predictors of metabolically unhealthy obesity in children and adolescents
Adiposity rebound in very-low-birth-weight infants
The association between a metabolically healthy overweight/obesity phenotype and markers of inflammation among Chinese children and adolescents aged 10–18 years
Case Reports
Management of perinatal HPP during critical illness/ECMO
Wolfram-like syndrome – another face of a rare disease in children
Two Japanese siblings with arginase-1 deficiency identified using a novel frameshift mutation of ARG1 (p.Lys41Thrfs∗2)
An atypical presentation of a pathogenic STK11 gene variant in siblings not fulfilling the clinical diagnostic criteria for Peutz-Jeghers Syndrome
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