Faculty of Medicine
OrgUnit's Researchers publications
(Dept/Workgroup Publication)
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Results 1-11 of 11 (Search time: 0.011 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 | 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 | First insights into the genetics of 21-hydroxylase deficiency in the Roma population | Mirjana Kocova ; Violeta Anastasovska ; Aleksandar Petlichkovski ; Henrik Falhammar | 19-Feb-2021 | Article | |
4 | Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia | Nikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia | 2020 | Article | |
5 | Implementation of Novel Mode for Evaluation of MYCN Amplification that can Predict Outcome in Patients with Neuroblastoma | Ilieva Gordana; Kocova Mirjana ; Conevska Biljana; Shukarova Angelovska, Elena | 2020 | Article | |
6 | 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 | |
7 | Leptin, obesity parameters and atopy among children with asthma | Cvejoska Cholakovska, Valentina ; Vlashki, Emilija ; Kochova, Mirjana ; Velikj Stefanovska, Vesna ; Petlichkovski, Aleksandar | 26-Oct-2021 | Article | |
8 | A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia | Violeta Anastasovska ; Mirjana Kocova ; Nikolina Zdraveska ; Maja Stojiljkovic; Anita Skakic; Kristel Klaassen; Sonja Pavlovic | 14-Mar-2021 | Article | |
9 | 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 | |
10 | Thyroid function and dysfunction in preterm infants-Challenges in evaluation, diagnosis and therapy | Zdraveska, Nikolina ; Kochova, Mirjana | Oct-2021 | Article | |
11 | 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 |
Organization name
Faculty of Medicine
Parent OrgUnit
City
Skopje
Country
Macedonia, the Former Yugoslav Republic of