Full Name
Anastasovska, Violeta
Main Affiliation
 
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Date Issued:  [2010 TO 2019]
Date Issued:  2018

Results 1-13 of 13 (Search time: 0.016 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
2Detection of Virus Herpes Simplex Type 1 in Patients with Chronic Periodontal DiseaseMarija Ivanovska-Stojanoska; Mirjana Popovska; Violeta Anastasovska ; Mirjana Kocova ; Lidita Zendeli-Bedzeti; Cena Dimova; Angela Taseva25-Sep-2018Article
3Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana 2018Article
4Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kochova, Mirjana Feb-2018Article
5Evaluation of selective newborn screening for inborn errors of metabolism in MacedoniaAnastasovska, Violeta ; Kochova, Mirjana 14-Oct-2018Proceeding article
6Incidence 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
7Molecular detection of virus herpes simplex type 1 (HSV-1), virus herpes simplex type 2 (HSV-2), Cytomegalovirus (HCMV) and Epstein-barr virus (EBV) in supra-gingival dental plaque in patients with periodontal disease.Ivanovska-Stojanoska, Marija; Popovska, Mirjana ; Anastasovska, Violeta ; Zendeli-Bedjeti, Lindita; Todorovska, SashkaDec-2018Article
8Molecular 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
9Rano 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
10Targeted 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
11Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-upMirjana Kocova ; Vesna Janevska ; Violeta Anastasovska Apr-2018Article
12Variations 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
13Неонатален скрининг во Република МакедонијаМирјана Кочова ; Виолета Анастасовска Dec-2018Article