Full Name
Anastasovska, Violeta
Main Affiliation
 
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Date Issued:  [2020 TO 2024]
Date Issued:  2020

Results 1-10 of 10 (Search time: 0.012 seconds).

PreviewTitleAuthor(s)Issue DateType
1Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyMirjana Kochova ; Violeta Anastasovska ; Henrik Falhammar2020Article
2Detection of the pathogenic CNVs in the Macedonian patient with profound developmental delayAnastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica6-Jun-2020Proceeding article
3Duplication of 10q22.2q23.1 as a cause for severe hypotonia in a childIlieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Naunova Timovska, Silvana ; Pesevska, Milica; Anastasovska, Violeta 6-Jun-2020Proceeding article
4Early onset of complex seizures as a first sign of 16p11.2 deletion syndromeShukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan6-Jun-2020Proceeding article
5First results from national newborn screening program for cystic fibrosis in the Republic of North MacedoniaFustikj, Stojka; Anastasovska, Violeta ; Plasheska-Karanfilska, Dijana; Spirevska, Lidija; Pesevska, Milica; Terzikj, Marija; Stamatova, Ana3-Jun-2020Proceeding article
6Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in MacedoniaNikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia2020Article
7Genomic and clinical characterisation of microduplications in a patient with developmental delayNestoroska, Dragica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Pesevska, Milica; Ilieva, Gordana6-Jun-2020Proceeding article
8Paediatric patient with deletion on chromosome 10q11.22 diagnosed by aCGHPesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana6-Jun-2020Proceeding article
9Thyroid peroxidase (TPO) mutations in Macedonian patients with congenital hypothyroidismZdraveska, Nikolina ; Anastasovska, Violeta ; Schoenmakers, Nadia; Nicholas, K. Adeline; Kochova, Mirjana 6-Jun-2020Proceeding article
10Современи методи во детекцијата на хромозомските аберацииШукарова-Ангеловска, Елена ; Анастасовска, Виолета ; Нестороска, Драгица; Петровска, Емилија10-Nov-2020Proceeding article