All Stories

  1. Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2017, De Gruyter

    PhD Violeta Anastasovska

  2. 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

  3. Phenylketonuria screening in the Republic of Macedonia

    Article • Orphanet Journal of Rare Diseases, August 2016, Springer Science + Business Media

    PhD Violeta Anastasovska

  4. 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

  5. Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of Macedonia

    Article • January 2016, De Gruyter

    PhD Violeta Anastasovska

  6. Clinical Practice: Experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia—a multiethnic country

    Article • European Journal of Pediatrics, September 2014, Springer Science + Business Media

    PhD Violeta Anastasovska

  7. Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase Deficiency/Direktna Molekularna Dijagnoza CYP21A2 Tačkaste Mutacije Kod Makedonskih I Srpskih Pacijenata Sa Nedostatkom 21-Hidroksilaze

    Article • January 2014, De Gruyter Open Sp. z o.o.

    PhD Violeta Anastasovska

  8. High Incidence of Congenital Hypothyroidism in One Region of the Republic of Macedonia

    Article • Balkan Journal of Medical Genetics, January 2014, De Gruyter Open Sp. z o.o.

    PhD Violeta Anastasovska

  9. Genotype-Phenotype Correlation in CAH Patients with Severe CYP21A2 Point Mutations in the Republic of Macedonia

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2010, De Gruyter

    PhD Violeta Anastasovska

  10. Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia

    Article • Balkan Journal of Medical Genetics, January 2010, De Gruyter Open Sp. z o.o.

    PhD Violeta Anastasovska

  11. A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia

    Article • Balkan Journal of Medical Genetics, January 2010, De Gruyter Open Sp. z o.o.

    PhD Violeta Anastasovska

  12. Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy

    Article • Balkan Journal of Medical Genetics, January 2007, De Gruyter Open Sp. z o.o.

    PhD Violeta Anastasovska