2. Repository of UKIM

Репозиториум на трудови на УКИМ


Anastasovska, Violeta

Network Lab View Statistics Email Alert RSS Feed

Profile

Full Name
Anastasovska, Violeta
Main Affiliation
 
Loading... 2 0 5 0 false
Loading... 3 0 5 0 false

Publications

Results 1-20 of 77 (Search time: 0.007 seconds).

ПрегледНасловАвтор(ите)Датум на издавањеТип
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-фев-2018Proceeding article
2BASELINE AND ACTH-STIMULATED SERUM 17-HYDROXYPROGESTERONE VALUES IN MACEDONIAN AND SERBIAN 21-HYDROXYLASE DEFICIENCY PATIENTSV. Anastasovska ; M. Kocova; M. Tanaskoska; S. Kuzmanovska 2014Proceeding article
3Chromosomal abnormalities in couples that undergo assisted reproduction technologiesShukarova Angelovska, Elena ; Ilieva, Gordana; Anastasovska, Violeta ; Hristova-Dimkovska, Tanja; Nestoroska, Dragica17-апр-2019Proceeding article
4Clinical and genomic characterization of 7q31.1 microduplication in a patient with developmental and neurological disabilitiesNestoroska, D; Anastasovska, V ; Shukarova Angelovska, E ; Pesevska, M; Veseli, A; Ilieva, G28-авг-2021Proceeding article
5Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMirjana Kochova ; Violeta Anastasovska ; Henrik Falhammar2020Article
6Clinical 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 Tasevaапр-2015Article
7Comments 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 дек-2015Article
8Coverage with Neonatal Thyroid Screening in the Republic of North Macedonia, during 2002–2020Pesevska, Milica; Anastasovska, Violeta ; Kocova, Mirjana ; Sukarova-Angelovska, Elena ; Fakovic, Nermina10-ное-2021Proceeding article
9Detected genotypes in Macedonian patients with simple virilizing form of congenital adrenal hyperplasiaAnastasovska, Violeta ; Kochova, Mirjana ; Shukarova Angelovska, Elena ; Zdraveska, Nikolina ; Ilieva, Gordana17-апр-2019Proceeding article
10Detected 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
11Detection of 3p25 microdeletion syndrome in the Macedonian patient with significant psychomotor retardationAnastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica; Stojanova, Ivana28-авг-2021Proceeding article
12Detection of giant chromosomal material on 7p+ with conventional karyotyping and aCGHIlieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Muaremoska-Kanzoska, Ljelja; Pesevska, Milica; Anastasovska, Violeta 28-авг-2021Proceeding article
13Detection of the pathogenic CNVs in the Macedonian patient with profound developmental delayAnastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica6-јун-2020Proceeding article
14Detection 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-сеп-2018Article
15Determination of monosomy 17 in anemia aplastica using fluorescence in situ hybridizationIlieva, Gordana; Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Koceva, Svetlana17-апр-2019Proceeding article
16Development delay in paediatric patient with deletion on chromosome 15q26.2Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana; Panovska, Sandra28-авг-2021Proceeding article
17Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana 2018Article
18Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kochova, Mirjana фев-2018Article
19The Diagnostic Value of Anti-Cyclic Citrullinated Peptide Antibodies (anti-CCP) in Patients with Rheumatoid ArthritisDamjanovska, LJubinka ; Anastasovska, Violeta ; Gruev, Todor1-дек-2007Article
20Different ethnical distribution of the incidence of cystic fibrosis in Republic of North MacedoniaAnastasovska, Violeta ; Fushtikj, Stojka ; Pesevska, Milica; Fakovic, Nermina; Stamatova, Ana9-јун-2021Proceeding article