Showing results 46 to 65 of 79
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| Preview | Title | Author(s) | Issue Date | Type |
| Methodological and organizational aspects of newborn screening for congenital hypothyroidism in Macedonia | Gjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana | Jul-2008 | Article |
| Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy | Anastasovska, V ; Kocova, M | 1-Jan-2007 | Article |
| Molecular detection of Herpes simplex virus type 1, Herpes simplex virus type 2, Cytomegalovirus and Epstein-barr virus in subgingival dental plaque in patients with periodontal disease | Ivanovska-Stojanovska, Marija; Popovska, Mirjana ; Anastasovska, Violeta ; Kochova, Mirjana ; Zendeli Bedjeti, Lindita; Atanasovska-Stojanovska, Aneta; Todorovska, Sashka | 17-Apr-2019 | Proceeding article |
| Molecular 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, Sashka | Dec-2018 | Article |
| Molecular diagnosis of MCAD in the Macedonian neonates with elevated medium-chain acylcarnitines identified through MS/MS-based newborn screening | Anastasovska, Violeta ; Kocova, Mirjana ; Zdraveska, Nikolina ; Tesovnik, Tine; Debeljak, Maruša; Kovač, Jernej | 2022 | Proceeding article |
| Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiency | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article |
| Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of Macedonia | Anastasovska Violeta ; Kocova Mirjana | Oct-2016 | Article |
| A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia | Violeta Anastasovska ; Mirjana Kocova ; Nikolina Zdraveska ; Maja Stojiljkovic; Anita Skakic; Kristel Klaassen; Sonja Pavlovic | 14-Mar-2021 | Article |
| A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia | Anastasovska, V ; Kocova, E; Kocova, M | 1-Jan-2010 | Article |
| Paediatric patient with deletion on chromosome 10q11.22 diagnosed by aCGH | Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana | 6-Jun-2020 | Proceeding article |
| Phenylketonuria screening in the Republic of Macedonia | Mirjana Kocova ; Violeta Anastasovska | 2016 | Article |
| Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years | Anastasovska, Violeta ; Pesevska, Milica; Zdraveska, Nikolina ; Zafirova, Biljana ; Meceska Jovcevska, Jasmina; Kochova, Mirjana | 2023 | Article |
| Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years | Anastasovska, Violeta ; Peshevska, Milica; Zdraveska, Nikolina ; Zafirova, Biljana ; Jovcevska Meceska, Jasmina; Kochova, Mirjana | 2023 | Article |
| Rano otkrivanje urođenih grešaka metabolizma neonatalnim skriningom – slučaj sa poremećajem u metabolizmu masnih kiselina srednjih lanaca | Zlateska, Snezana; Anastasovska, Violeta ; Zlateska, Sofija; Zlateska, A | 20-Sep-2018 | Proceeding article |
| Regional Variation in the Incidence of Congenital Hypothyroidism in Macedonia | Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Pesevska; Elizabeta Taseva; Mirjana Kocova | 21-Aug-2017 | Article |
| Results from a newborn screening (NBS) pilot study for cystic fibrosis in the Republic of Macedonia. | Fustik, Stojka; Anastasovska, Violeta ; Plasheska Karanfilska, Dijana; Spirevska, Lidija; Stamatova, Ana; Pesevska, Milica; Terzic, Marija | 5-Jun-2019 | Proceeding article |
| Seven years experience with selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kocova Mirjana ; Shukarova Angelovska, Elena ; Pesevska, Milica; Zdraveska, Nikolina | 10-Nov-2021 | Proceeding article |
 | The spectrum of CFTR mutations in newly diagnosed cases of cystic fibrosis through newborn screening in the Republic of North Macedonia | Fustik, Stojka ; Anastasovska, Violeta ; Plaseska Karanfilska, Dijana; Stamatova, Ana; Spirevska, Lidija; Pesevska, Milica; Terzikj, Marija; Vujovic, Marija | Jun-2022 | Proceeding article |
| Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood | Mirjana Kocova ; Nikolina Zdraveska ; Maja Zdravkovska ; Violeta Anastasovska ; Daniela Pop Gjorceva | 2016 | Article |
| Targeted sequencing of dyshormonogenesis-associated genes in Macedonian cases with congenital hypothyroidism and gland-in-situ reveals a low mutation frequency | Zdraveska, Nikolina ; Kocova, Mirjana ; Nicholas, Adeline K; Anastasovska, Violeta ; Schoenmakers, Nadia | 2-Nov-2018 | Proceeding article |
