Anastasovska, Violeta
Full Name
Anastasovska, Violeta
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Results 1-10 of 10 (Search time: 0.012 seconds).
Preview | Title | Author(s) | Issue Date | Type | |
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1 | Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Mirjana Kochova ; Violeta Anastasovska ; Henrik Falhammar | 2020 | Article | |
2 | 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 | |
3 | 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 | |
4 | 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 | |
5 | 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 | |
6 | Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia | Nikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia | 2020 | Article | |
7 | 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 | |
8 | 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 | |
9 | 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 | |
10 | Современи методи во детекцијата на хромозомските аберации | Шукарова-Ангеловска, Елена ; Анастасовска, Виолета ; Нестороска, Драгица; Петровска, Емилија | 10-Nov-2020 | Proceeding article |