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Published/Copyright: June 2, 2018

Published Online: 2018-6-2
Published in Print: 2018-6-27

©2018 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Editorial
  3. Congenital hypothyroidism
  4. Original Articles
  5. Does initial dosing of levothyroxine in infants with congenital hypothyroidism lead to frequent dose adjustments secondary to iatrogenic hyperthyroidism on follow-up?
  6. Incidence of congenital hypothyroidism in China: data from the national newborn screening program, 2013–2015
  7. The etiologies and incidences of congenital hypothyroidism before and after neonatal TSH screening program implementation: a study in southern Thailand
  8. Current status of the congenital hypothyroidism neonatal screening program in Adana Province, Turkey
  9. Risk of hypoglycemia in youth with type 2 diabetes on insulin
  10. Metabolic risk factors in adolescent girls with type 1 diabetes
  11. Definition of reference ranges for β-isomerized carboxy-terminal telopeptide collagen type I for children and adolescents
  12. Brown adipose tissue in young adults who were born preterm or small for gestational age
  13. Circulating soluble RAGE and cell surface RAGE on peripheral blood mononuclear cells in healthy children
  14. Predictors of bone maturation, growth rate and adult height in children with central precocious puberty treated with depot leuprolide acetate
  15. Trends in the use of puberty blockers among transgender children in the United States
  16. Initial presentations and associated clinical findings in patients with classical congenital adrenal hyperplasia
  17. Cardiac examination in children with Laron syndrome undergoing mecasermin therapy
  18. Five novel ALMS1 gene mutations in six patients with Alström syndrome
  19. Case Reports
  20. Cutaneous mucormycosis as a presenting feature of type 1 diabetes in a boy – case report and review of the literature
  21. Severe lactic acidosis in an extremely low birth weight infant due to thiamine deficiency
  22. Exertional rhabdomyolysis in carbonic anhydrase 12 deficiency
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