Published in J Pediatr Endocrinol Metab on October 01, 2009
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis. Eur J Endocrinol (2007) 1.14
Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome. Eur J Pediatr (2008) 0.78
Transient neonatal hypothyroidism manifested at birth. J Pediatr Endocrinol Metab (2009) 0.75
Thyroid volume and urinary iodine excretion in schoolchildren in North-Eastern Bosnia. Eur J Pediatr (2004) 0.75
Health-related quality of life in children and adolescents with type 1 diabetes mellitus from Montenegro: relationship to metabolic control. J Pediatr Endocrinol Metab (2016) 0.75