Showing results 1 to 20 of 79
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| Preview | Title | Author(s) | Issue Date | Type |
| 46, XX DSD with diphallus as a part of a multimalformative syndrome - a case report | Shukarova Angelovska, Elena ; Kochova, Mirjana ; Ilieva, Gordana; Anastasovska, Violeta ; Krstevska Konstantinova, Marina ; Filev, G | 23-Feb-2018 | Proceeding article |
| BASELINE AND ACTH-STIMULATED SERUM 17-HYDROXYPROGESTERONE VALUES IN MACEDONIAN AND SERBIAN 21-HYDROXYLASE DEFICIENCY PATIENTS | V. Anastasovska ; M. Kocova; M. Tanaskoska; S. Kuzmanovska | 2014 | Proceeding article |
| Chromosomal abnormalities in couples that undergo assisted reproduction technologies | Shukarova Angelovska, Elena ; Ilieva, Gordana; Anastasovska, Violeta ; Hristova-Dimkovska, Tanja; Nestoroska, Dragica | 17-Apr-2019 | Proceeding article |
| Clinical and genomic characterization of 7q31.1 microduplication in a patient with developmental and neurological disabilities | Nestoroska, D; Anastasovska, V ; Shukarova Angelovska, E ; Pesevska, M; Veseli, A; Ilieva, G | 28-Aug-2021 | Proceeding article |
| Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Mirjana Kochova ; Violeta Anastasovska ; Henrik Falhammar | 2020 | Article |
| Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic country | Mirjana Kocova ; Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Tanaskoska; Elizabeta Taseva | Apr-2015 | Article |
| Comments 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. Battelino | Mirjana Kocova ; Violeta Anastasovska | Dec-2015 | Article |
| Coverage with Neonatal Thyroid Screening in the Republic of North Macedonia, during 2002–2020 | Pesevska, Milica; Anastasovska, Violeta ; Kocova, Mirjana ; Sukarova-Angelovska, Elena ; Fakovic, Nermina | 10-Nov-2021 | Proceeding article |
| Detected genotypes in Macedonian patients with simple virilizing form of congenital adrenal hyperplasia | Anastasovska, Violeta ; Kochova, Mirjana ; Shukarova Angelovska, Elena ; Zdraveska, Nikolina ; Ilieva, Gordana | 17-Apr-2019 | Proceeding article |
| Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relatives | Anastasovska Violeta ; Kocova Mirjana | 2010 | Article |
| Detection of 3p25 microdeletion syndrome in the Macedonian patient with significant psychomotor retardation | Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica; Stojanova, Ivana | 28-Aug-2021 | Proceeding article |
| Detection of giant chromosomal material on 7p+ with conventional karyotyping and aCGH | Ilieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Muaremoska-Kanzoska, Ljelja; Pesevska, Milica; Anastasovska, Violeta | 28-Aug-2021 | Proceeding article |
| Detection of the pathogenic CNVs in the Macedonian patient with profound developmental delay | Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica | 6-Jun-2020 | Proceeding article |
| Detection of Virus Herpes Simplex Type 1 in Patients with Chronic Periodontal Disease | Marija Ivanovska-Stojanoska; Mirjana Popovska; Violeta Anastasovska ; Mirjana Kocova ; Lidita Zendeli-Bedzeti; Cena Dimova; Angela Taseva | 25-Sep-2018 | Article |
| Determination of monosomy 17 in anemia aplastica using fluorescence in situ hybridization | Ilieva, Gordana; Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Koceva, Svetlana | 17-Apr-2019 | Proceeding article |
| Development delay in paediatric patient with deletion on chromosome 15q26.2 | Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana; Panovska, Sandra | 28-Aug-2021 | Proceeding article |
| Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism | Zdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana | 2018 | Article |
| Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism | Zdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kochova, Mirjana | Feb-2018 | Article |
| The Diagnostic Value of Anti-Cyclic Citrullinated Peptide Antibodies (anti-CCP) in Patients with Rheumatoid Arthritis | Damjanovska, LJubinka ; Anastasovska, Violeta ; Gruev, Todor | 1-Dec-2007 | Article |
| Different ethnical distribution of the incidence of cystic fibrosis in Republic of North Macedonia | Anastasovska, Violeta ; Fushtikj, Stojka ; Pesevska, Milica; Fakovic, Nermina; Stamatova, Ana | 9-Jun-2021 | Proceeding article |
