Faculty of Medicine
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| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 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 | 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 | |
| 3 | Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia | Nikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia | 2020 | Article | |
| 4 | 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 | |
| 5 | 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 | |
| 6 | 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 | |
| 7 | Thyroid function and dysfunction in preterm infants-Challenges in evaluation, diagnosis and therapy | Zdraveska, Nikolina ; Kochova, Mirjana | Oct-2021 | Article |
Organization name
Faculty of Medicine
Parent OrgUnit
City
Skopje
Country
Macedonia, the Former Yugoslav Republic of