Full Name
Zdraveska, Nikolina
Main Affiliation
 
Email
n.zdraveska@medf.ukim.edu.mk
 
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Date Issued:  [2020 TO 2024]

Results 1-7 of 7 (Search time: 0.008 seconds).

PreviewTitleAuthor(s)Issue DateType
1Detection of 3p25 microdeletion syndrome in the Macedonian patient with significant psychomotor retardationAnastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica; Stojanova, Ivana28-Aug-2021Proceeding article
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
3ESHG 2022 , P04.021.D.png.jpgGenetics of transient congenital hypothyroidismZdraveska, Nikolina ; Anastasovska, Violeta ; Kocova Mirjana 11-Jun-2022Proceeding article
4Molecular diagnosis of MCAD in the Macedonian neonates with elevated medium-chain acylcarnitines identified through MS/MS-based newborn screeningAnastasovska, Violeta ; Kocova, Mirjana ; Zdraveska, Nikolina ; Tesovnik, Tine; Debeljak, Maruša; Kovač, Jernej2022Proceeding article
5Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty yearsAnastasovska, Violeta ; Pesevska, Milica; Zdraveska, Nikolina ; Zafirova, Biljana ; Meceska Jovcevska, Jasmina; Kochova, Mirjana 2023Article
6Seven years experience with selective newborn screening for inborn errors of metabolism in MacedoniaAnastasovska, Violeta ; Kocova Mirjana ; Shukarova Angelovska, Elena ; Pesevska, Milica; Zdraveska, Nikolina 10-Nov-2021Proceeding article
7Thyroid peroxidase (TPO) mutations in Macedonian patients with congenital hypothyroidismZdraveska, Nikolina ; Anastasovska, Violeta ; Schoenmakers, Nadia; Nicholas, K. Adeline; Kochova, Mirjana 6-Jun-2020Proceeding article