OrgUnit's Researchers publications
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Date Issued:  [2020 TO 2021]
Author:  Mirjana Kochova
Fulltext:  No Fulltext

Results 1-5 of 5 (Search time: 0.019 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
2First insights into the genetics of 21-hydroxylase deficiency in the Roma populationMirjana Kocova ; Violeta Anastasovska ; Aleksandar Petlichkovski ; Henrik Falhammar19-Feb-2021Article
3Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in MacedoniaNikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia2020Article
4A 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
5Thyroid function and dysfunction in preterm infants-Challenges in evaluation, diagnosis and therapyZdraveska, Nikolina ; Kochova, Mirjana Oct-2021Article

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