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Anastasovska, Violeta
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Author:  Anastasovska, Violeta
Type:  Proceeding article
Date Issued:  2018

Results 1-7 of 7 (Search time: 0.007 seconds).

PreviewTitleAuthor(s)Issue DateType
146, XX DSD with diphallus as a part of a multimalformative syndrome - a case reportShukarova Angelovska, Elena ; Kochova, Mirjana ; Ilieva, Gordana; Anastasovska, Violeta ; Krstevska Konstantinova, Marina ; Filev, G23-Feb-2018Proceeding article
2Evaluation of selective newborn screening for inborn errors of metabolism in MacedoniaAnastasovska, Violeta ; Kochova, Mirjana 14-Oct-2018Proceeding article
3Incidence of congenital hypothyroidism in different regions of Macedonia - sixteen years newborn thyroid screeningAnastasovska, Violeta ; Pesevska, Milica; Taseva, Elizabeta; Sukarova-Angelovska, Elena; Zdraveska, Nikolina ; Gurzanova-Durnev Ljiljana; Kochova, Mirjana 3-Oct-2018Proceeding article
4Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiencyAnastasovska, Violeta ; Kochova, Mirjana 14-Oct-2018Proceeding article
5Rano otkrivanje urođenih grešaka metabolizma neonatalnim skriningom – slučaj sa poremećajem u metabolizmu masnih kiselina srednjih lanacaZlateska, Snezana; Anastasovska, Violeta ; Zlateska, Sofija; Zlateska, A20-Sep-2018Proceeding article
6Targeted sequencing of dyshormonogenesis-associated genes in Macedonian cases with congenital hypothyroidism and gland-in-situ reveals a low mutation frequencyZdraveska, Nikolina ; Kocova, Mirjana ; Nicholas, Adeline K; Anastasovska, Violeta ; Schoenmakers, Nadia2-Nov-2018Proceeding article
7Variations in incidence of congenital hypothyroidism in association with changes of cutoff valuePesevska, Milica; Anastasovska, Violeta ; Taseva, Elizabeta; Zdraveska, Nikolina ; Gurzanova-Durnev, Liljana; Kochova, Mirjana 3-Oct-2018Proceeding article