All Stories

  1. Genetic spectrum of neonatal diabetes

    Article • Balkan Journal of Medical Genetics, November 2020, De Gruyter

    Prof Dr Mirjna Kocova

  2. Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis

    Article • Balkan Journal of Medical Genetics, December 2019, De Gruyter

    Prof Dr Mirjna Kocova

  3. Genetic arterial anomaly in two families from the Republic of Macedonia

    Article • Balkan Journal of Medical Genetics, October 2018, De Gruyter

    Prof Dr Mirjna Kocova

  4. Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-up

    Article • Endocrine Connections, March 2018, Bioscientifica

    Prof Dr Mirjna Kocova

  5. Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism

    Article • Endocrine Connections, January 2018, Bioscientifica

    Prof Dr Mirjna Kocova

  6. Old syndrome–new approach: Mauriac syndrome treated with continuous insulin delivery

    Article • SAGE Open Medical Case Reports, January 2018, SAGE Publications

    Prof Dr Mirjna Kocova

  7. Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood

    Article • SAGE Open Medical Case Reports, December 2016, SAGE Publications

    PhD Violeta Anastasovska, Prof Dr Mirjna Kocova

  8. Diagnostic approach in children with unusual symptoms of acquired hypothyroidism. When to look for pituitary hyperplasia?

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2016, De Gruyter

    Prof Dr Mirjna Kocova

  9. Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2016, De Gruyter

    Prof Dr Mirjna Kocova, PhD Violeta Anastasovska