Anastasovska, Violeta
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Anastasovska, Violeta
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Results 1-20 of 23 (Search time: 0.014 seconds).
| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 1 | 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 | |
| 2 | 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 | |
| 3 | 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 | |
| 4 | 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 | |
| 5 | 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 | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | Duplication of 10q22.2q23.1 as a cause for severe hypotonia in a child | Ilieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Naunova Timovska, Silvana ; Pesevska, Milica; Anastasovska, Violeta | 6-Jun-2020 | Proceeding article | |
| 9 | Early onset of complex seizures as a first sign of 16p11.2 deletion syndrome | Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan | 6-Jun-2020 | Proceeding article | |
| 10 | First results from national newborn screening program for cystic fibrosis in the Republic of North Macedonia | Fustikj, Stojka; Anastasovska, Violeta ; Plasheska-Karanfilska, Dijana; Spirevska, Lidija; Pesevska, Milica; Terzikj, Marija; Stamatova, Ana | 3-Jun-2020 | Proceeding article | |
| 11 |  | Genetics of transient congenital hypothyroidism | Zdraveska, Nikolina ; Anastasovska, Violeta ; Kocova Mirjana | 11-Jun-2022 | Proceeding article |
| 12 | Genomic and clinical characterisation of microduplications in a patient with developmental delay | Nestoroska, Dragica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Pesevska, Milica; Ilieva, Gordana | 6-Jun-2020 | Proceeding article | |
| 13 | Incidence of Congenital Hypothyroidism in the Republic of North Macedonia in Correlation with TSH Cutoff Level | Anastasovska, Violeta ; Pesevska, Milica; Kocova, Mirjana ; Shukarova Angelovska, Elena ; Fakovic, Nermina; Karishik, Senada | 10-Nov-2021 | Proceeding article | |
| 14 | Introduction of neonatal screening for cystic fibrosis in the Republic of North Macedonia | Anastasovska, Violeta ; Pesevska, Milica; Fustik, Stojka ; Stamatova, Ana | 10-Nov-2021 | Proceeding article | |
| 15 | 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 | |
| 16 | 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 | |
| 17 | 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 | |
| 18 | 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 | |
| 19 |  | 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 |
| 20 | Thyroid peroxidase (TPO) mutations in Macedonian patients with congenital hypothyroidism | Zdraveska, Nikolina ; Anastasovska, Violeta ; Schoenmakers, Nadia; Nicholas, K. Adeline; Kochova, Mirjana | 6-Jun-2020 | Proceeding article |