| Preview | Title | Author(s) | Issue Date | Type |
| 1 | | Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic country | Mirjana Kocova ; Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Tanaskoska; Elizabeta Taseva | Apr-2015 | Article |
| 2 | | Clinical variability in two Macedonian families with Arterial tortuosity syndrome | M Kocova ; R Kacarska ; K Kuzevska-Maneva ; S Prijic; M Lazareska; C Dordoni; M Ritelli; M Colombi | 29-Oct-2018 | Article |
| 3 | | Comment on Publications from OpT2mise Study | Tatjana Milenkovic ; Mirjana Kocova ; Brankica Krstevska; Gordana Pemovska ; Ivica Smokovski | 2016 | Article |
| 4 | | Comments on 'Newborn screening in southeastern Europe' published in Molecular Genetics and Metabolism, 2014 Sept-Oct;113(1-2):42-45 by U. Groselj, M. ZerjavTansek, A. Smon, N. Angelkova, D. Anton, I. Baric, M. Djordjevic, L. Grimci, M. Ivanova, A. Kadam, V. Mulliqi Kotori, H. Maksic, O. Marginean, O. Margineanu, O. Milijanovic, F. Moldovanu, M. Muresan, S. Murko, M. Nanu, B. Repic Lampert, M. Samardzic, V. Sarnavka, A. Savov, M. Stojiljkovic, B. Suzic, R. Tincheva, H. Tahirovic, A. Toromanovic, N. Usurela, T. Battelino | Mirjana Kocova ; Violeta Anastasovska | Dec-2015 | Article |
| 5 | | Correlation of serum adiponectin and leptin concentrations with anthropometric parameters in newborns | Palcevska-Kocevska, Snezana; Aluloska, Natasa; Krstevska, Marija ; Shukarova-Angelovska, Elena ; Kojik, Ljiljana; Zisovska, Elizabeta; Kocevski, Dragoslav ; Kocova, Mirjana | 2012 | Article |
| 6 | | Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relatives | Anastasovska Violeta ; Kocova Mirjana | 2010 | Article |
| 7 | | Detection of Virus Herpes Simplex Type 1 in Patients with Chronic Periodontal Disease | Marija Ivanovska-Stojanoska; Mirjana Popovska; Violeta Anastasovska ; Mirjana Kocova ; Lidita Zendeli-Bedzeti; Cena Dimova; Angela Taseva | 25-Sep-2018 | Article |
| 8 | | Diagnostic approach in children with unusual symptoms of acquired hypothyroidism. When to look for pituitary hyperplasia? | Mirjana Kocova ; Nikolina Zdraveska ; Rozana Kacarska ; Elena Kochova | Mar-2016 | Article |
| 9 | | Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism | Zdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kochova, Mirjana | Feb-2018 | Article |
| 10 | | Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase Deficiency | Anastasovska Violeta ; Milenković Tatjana ; Kocova Mirjana | Jan-2015 | Article |
| 11 | | Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies | Pörksen, Sven; Laborie, Lene Bjerke; Nielsen, Lotte; Louise Max Andersen, Marie; Sandal, Tone; de Wet, Heidi; Schwarcz, Erik; Aman, Jan; Swift, Peter; Kocova, Mirjana ; Schönle, Eugen J; de Beaufort, Carine; Hougaard, Philip; Ashcroft, Frances; Molven, Anders; Knip, Mikael; Mortensen, Henrik B; Hansen, Lars; Njølstad, Pål R | 23-Sep-2010 | Article |
| 12 | | Efficacy and safety of a fixed combination of insulin degludec/insulin aspart in children and adolescents with type 1 diabetes: A randomized trial | Battelino, Tadej; Deeb, Larry C; Ekelund, Magnus; Kinduryte, Ona; Klingensmith, Georgeanna J; Kocova, Mirjana ; Kovarenko, Margarita; Shehadeh, Naim | 2018 | Article |
| 13 | | Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia | Violeta Anastasovska ; Mirjana Kocova | 1-Apr-2017 | Article |
| 14 | | Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism | Nikolina Zdraveska ; Violeta Anastasovska ; Mirjana Kocova | 1-Jul-2016 | Article |
| 15 | | Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of Macedonia | Violeta Anastasovska ; Mirjana Kocova | Sep-2010 | Article |
| 16 | | High incidence of congenital hypothyroidism in one region of the Republic of Macedonia | V Anastasovska ; R Koviloska; M Kocova | Jun-2014 | Article |
| 17 | | The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family | Mirjana Kocova ; Violeta Anastasovska ; Iskra Bitovska | 19-Jun-2019 | Article |
| 18 | | Impact of Lower Screening TSH Cutoff Level on the Increasing Prevalence of Congenital Hypothyroidism | Anastasovska, Violeta ; Kocova, Mirjana | 4-Apr-2017 | Article |
| 19 | | Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia | Anastasovska, V ; Kocova, M | 1-Jan-2010 | Article |
| 20 | | The many faces of oral-facial-digital syndrome | E Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova | Jun-2012 | Article |
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