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Anxiety, pediatric type 1 diabetes and COVID-19 lockdown
-
Sookaromdee Pathum
and
Wiwanitkit Viroj
Published/Copyright:
May 17, 2022
Received: 2022-03-28
Accepted: 2022-04-25
Published Online: 2022-05-17
Published in Print: 2022-06-27
© 2022 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Review Articles
- The genetic elucidation of monogenic obesity in the Arab world: a systematic review
- Global perspective on pediatric growth hormone registries: a systematic review
- Mini Review
- Considering metformin as a second-line treatment for children and adolescents with prediabetes
- Original Articles
- Central adrenal insufficiency screening with morning plasma cortisol and ACTH levels in Prader–Willi syndrome
- Clinical characteristics and genetics analysis for the ITD of congenital hypothyroidism
- Genomic landscape of sporadic pediatric differentiated thyroid cancers: a systematic review and meta-analysis
- The role of circulating miRNAs in leptin resistance in obese children
- Relationship between height age, bone age and chronological age in normal children in the context of nutritional and pubertal status
- Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescents
- Ten year analysis of the clinic profile of the tertiary paediatric endocrine service in Western Australia
- Postoperative intensive care management and residual endocrinopathy of pediatric supratentorial brain tumors: a retrospective cohort study
- Successful telehealth transformation of a pediatric outpatient obesity teaching program due to the COVID-19 pandemic – the “Video KiCK” program
- Glycemic control among children with type 1 diabetes mellitus and its determinants in a resource-limited setting
- Letter to the Editor
- Anxiety, pediatric type 1 diabetes and COVID-19 lockdown
- Short Communication
- Ethnic diversity and burden of polycystic ovary syndrome among US adolescent females
- Case Reports
- Feminizing adrenocortical oncocytoma presenting as precocious puberty: a case report and literature review
- Novel OTX2 loss of function variant associated with congenital hypopituitarism without eye abnormalities
- Bilateral Wilms’ tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region
- A very rare cause of arthrogryposis multiplex congenita: a novel mutation in TOR1A
