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Anastasovska, Violeta

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Anastasovska, Violeta
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Results 1-20 of 28 (Search time: 0.036 seconds).

PreviewTitleAuthor(s)Issue DateType
1Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMirjana Kochova ; Violeta Anastasovska ; Henrik Falhammar2020Article
2Clinical 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
3Comments 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
4Detected 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
5Detection 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
6Diagnostic 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
7Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase DeficiencyAnastasovska Violeta ; Milenković Tatjana ; Kocova Mirjana Jan-2015Article
8Ethnicity and incidence of congenital hypothyroidism in the capital of MacedoniaVioleta Anastasovska ; Mirjana Kocova 1-Apr-2017Article
9First insights into the genetics of 21-hydroxylase deficiency in the Roma populationMirjana Kocova ; Violeta Anastasovska ; Aleksandar Petlichkovski ; Henrik Falhammar19-Feb-2021Article
10Frequency 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
11Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in MacedoniaNikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia2020Article
12Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of MacedoniaVioleta Anastasovska ; Mirjana Kocova Sep-2010Article
13High incidence of congenital hypothyroidism in one region of the Republic of MacedoniaV Anastasovska ; R Koviloska; M Kocova Jun-2014Article
14The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one familyMirjana Kocova ; Violeta Anastasovska ; Iskra Bitovska19-Jun-2019Article
15Impact of Lower Screening TSH Cutoff Level on the Increasing Prevalence of Congenital HypothyroidismAnastasovska, Violeta ; Kocova, Mirjana 4-Apr-2017Article
16Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of MacedoniaAnastasovska, V ; Kocova, M 1-Jan-2010Article
17Methodological and organizational aspects of newborn screening for congenital hypothyroidism in MacedoniaGjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana Jul-2008Article
18Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype DiscrepancyAnastasovska, V ; Kocova, M 1-Jan-2007Article
19Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of MacedoniaAnastasovska Violeta ; Kocova Mirjana Oct-2016Article
20A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasiaVioleta Anastasovska ; Mirjana Kocova ; Nikolina Zdraveska ; Maja Stojiljkovic; Anita Skakic; Kristel Klaassen; Sonja Pavlovic14-Mar-2021Article