Full Name
Anastasovska, Violeta
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Results 1-20 of 21 (Search time: 0.015 seconds).

PreviewTitleAuthor(s)Issue DateType
1Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic countryMirjana Kocova ; Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Tanaskoska; Elizabeta TasevaApr-2015Article
2Comments on 'Newborn screening in southeastern Europe' published in Molecular Genetics and Metabolism, 2014 Sept-Oct;113(1-2):42-45 by U. Groselj, M. ZerjavTansek, A. Smon, N. Angelkova, D. Anton, I. Baric, M. Djordjevic, L. Grimci, M. Ivanova, A. Kadam, V. Mulliqi Kotori, H. Maksic, O. Marginean, O. Margineanu, O. Milijanovic, F. Moldovanu, M. Muresan, S. Murko, M. Nanu, B. Repic Lampert, M. Samardzic, V. Sarnavka, A. Savov, M. Stojiljkovic, B. Suzic, R. Tincheva, H. Tahirovic, A. Toromanovic, N. Usurela, T. BattelinoMirjana Kocova ; Violeta Anastasovska Dec-2015Article
3Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relativesAnastasovska Violeta ; Kocova Mirjana 2010Article
4Detection 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
5Diagnostic 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
6Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase DeficiencyAnastasovska Violeta ; Milenković Tatjana ; Kocova Mirjana Jan-2015Article
7Ethnicity and incidence of congenital hypothyroidism in the capital of MacedoniaVioleta Anastasovska ; Mirjana Kocova 1-Apr-2017Article
8Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidismNikolina Zdraveska ; Violeta Anastasovska ; Mirjana Kocova 1-Jul-2016Article
9Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of MacedoniaVioleta Anastasovska ; Mirjana Kocova Sep-2010Article
10High incidence of congenital hypothyroidism in one region of the Republic of MacedoniaV Anastasovska ; R Koviloska; M Kocova Jun-2014Article
11The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one familyMirjana Kocova ; Violeta Anastasovska ; Iskra Bitovska19-Jun-2019Article
12Impact of Lower Screening TSH Cutoff Level on the Increasing Prevalence of Congenital HypothyroidismAnastasovska, Violeta ; Kocova, Mirjana 4-Apr-2017Article
13Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of MacedoniaAnastasovska, V ; Kocova, M 1-Jan-2010Article
14Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of MacedoniaAnastasovska Violeta ; Kocova Mirjana Oct-2016Article
15A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal HyperplasiaAnastasovska, V ; Kocova, E; Kocova, M 1-Jan-2010Article
16Phenylketonuria screening in the Republic of MacedoniaMirjana Kocova ; Violeta Anastasovska 2016Article
17Regional Variation in the Incidence of Congenital Hypothyroidism in MacedoniaVioleta Anastasovska ; Elena Sukarova-Angelovska ; Milica Pesevska; Elizabeta Taseva; Mirjana Kocova 21-Aug-2017Article
18Submental thyroid ectopy might cause subclinical hypothyroidism in early childhoodMirjana Kocova ; Nikolina Zdraveska ; Maja Zdravkovska ; Violeta Anastasovska ; Daniela Pop Gjorceva 2016Article
19Targeted 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
20Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-upMirjana Kocova ; Vesna Janevska ; Violeta Anastasovska Apr-2018Article