Anastasovska, Violeta
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Anastasovska, Violeta
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Results 1-20 of 20 (Search time: 0.009 seconds).
Preview | Title | Author(s) | Issue Date | Type | |
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1 | 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 | |
2 | 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 | |
3 | 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 | |
4 | 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 | |
5 | 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 | |
6 | 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 | |
7 | 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 | |
8 | 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 | |
9 | 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 | |
10 | 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 | |
11 | Incidence of congenital hypothyroidism in different regions of Macedonia - sixteen years newborn thyroid screening | Anastasovska, Violeta ; Pesevska, Milica; Taseva, Elizabeta; Sukarova-Angelovska, Elena; Zdraveska, Nikolina ; Gurzanova-Durnev Ljiljana; Kochova, Mirjana | 3-Oct-2018 | Proceeding article | |
12 | 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 | |
13 | 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 | |
14 | 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 | |
15 | 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 | |
16 | 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 | |
17 | 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 | |
18 | 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 | |
19 | Two-year neonatal screening for cystic fibrosis in Republic of North Macedonia | Fustik, Stojka; Anastasovska, Violeta ; Plaseska-Karanfilska, Dijana; Stamatova, Ana; Spirevska, Lidija; Pesevska, Milica; Terzic, Marija; Fakovic, Nermina | 9-Jun-2021 | Proceeding article | |
20 | Variations in incidence of congenital hypothyroidism in association with changes of cutoff value | Pesevska, Milica; Anastasovska, Violeta ; Taseva, Elizabeta; Zdraveska, Nikolina ; Gurzanova-Durnev, Liljana; Kochova, Mirjana | 3-Oct-2018 | Proceeding article |