OrgUnit's Researchers publications
(Dept/Workgroup Publication)

Refined By:
Date Issued:  [2020 TO 2021]
Author:  Kocova, Mirjana

Results 1-11 of 11 (Search time: 0.011 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
2Coverage with Neonatal Thyroid Screening in the Republic of North Macedonia, during 2002–2020Pesevska, Milica; Anastasovska, Violeta ; Kocova, Mirjana ; Sukarova-Angelovska, Elena ; Fakovic, Nermina10-Nov-2021Proceeding article
3First insights into the genetics of 21-hydroxylase deficiency in the Roma populationMirjana Kocova ; Violeta Anastasovska ; Aleksandar Petlichkovski ; Henrik Falhammar19-Feb-2021Article
4Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in MacedoniaNikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia2020Article
5Implementation of Novel Mode for Evaluation of MYCN Amplification that can Predict Outcome in Patients with NeuroblastomaIlieva Gordana; Kocova Mirjana ; Conevska Biljana; Shukarova Angelovska, Elena 2020Article
6Incidence of Congenital Hypothyroidism in the Republic of North Macedonia in Correlation with TSH Cutoff LevelAnastasovska, Violeta ; Pesevska, Milica; Kocova, Mirjana ; Shukarova Angelovska, Elena ; Fakovic, Nermina; Karishik, Senada10-Nov-2021Proceeding article
7Leptin, obesity parameters and atopy among children with asthmaCvejoska Cholakovska, Valentina ; Vlashki, Emilija ; Kochova, Mirjana ; Velikj Stefanovska, Vesna ; Petlichkovski, Aleksandar 26-Oct-2021Article
8A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasiaVioleta Anastasovska ; Mirjana Kocova ; Nikolina Zdraveska ; Maja Stojiljkovic; Anita Skakic; Kristel Klaassen; Sonja Pavlovic14-Mar-2021Article
9Seven 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
10Thyroid function and dysfunction in preterm infants-Challenges in evaluation, diagnosis and therapyZdraveska, Nikolina ; Kochova, Mirjana Oct-2021Article
11Thyroid peroxidase (TPO) mutations in Macedonian patients with congenital hypothyroidismZdraveska, Nikolina ; Anastasovska, Violeta ; Schoenmakers, Nadia; Nicholas, K. Adeline; Kochova, Mirjana 6-Jun-2020Proceeding article

Organization name
Faculty of Medicine
City
Skopje
Country
Macedonia, the Former Yugoslav Republic of