| Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism N Zdraveska, M Zdravkovska, V Anastasovska, E Sukarova-Angelovska, ... Endocrine connections 7 (2), 278-285, 2018 | 41 | 2018 |
| Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-up M Kocova, V Janevska, V Anastasovska Endocrine connections 7 (4), 544-552, 2018 | 27 | 2018 |
| European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance A Munck, DO Berger, KW Southern, C Carducci, KM de Winter-de Groot, ... Journal of Cystic Fibrosis 22 (3), 484-495, 2023 | 26 | 2023 |
| Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency M Kocova, V Anastasovska, H Falhammar Endocrine 69 (2), 262-277, 2020 | 26 | 2020 |
| Clinical practice: Experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia—A multiethnic country M Kocova, V Anastasovska, E Sukarova-Angelovska, M Tanaskoska, ... European journal of pediatrics 174, 443-448, 2015 | 24 | 2015 |
| Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia V Anastasovska, M Kocova Journal of Pediatric Endocrinology and Metabolism 30 (4), 405-409, 2017 | 23 | 2017 |
| Reliability of neonatal screening results M Knapkova, K Hall, G Loeber International journal of neonatal screening 4 (3), 28, 2018 | 20 | 2018 |
| High incidence of congenital hypothyroidism in one region of the republic of macedonia V Anastasovska, R Koviloska, M Kocova Balkan Journal of Medical Genetics 17 (1), 31-35, 2014 | 20 | 2014 |
| Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia N Zdraveska, M Kocova, AK Nicholas, V Anastasovska, N Schoenmakers Frontiers in endocrinology 11, 413, 2020 | 16 | 2020 |
| Detection of virus herpes simplex type 1 in patients with chronic periodontal disease M Ivanovska-Stojanoska, M Popovska, V Anastasovska, M Kocova, ... Open Access Macedonian Journal of Medical Sciences 6 (9), 1737, 2018 | 15 | 2018 |
| Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of Macedonia V Anastasovska, M Kocova Walter de Gruyter GmbH & Co. KG 23 (9), 921-926, 2010 | 15 | 2010 |
| Effects of different dietary fatty acid supplements upon lipoprotein metabolism and lipid peroxides production in hyperlipidemic rats. J Dimitrova Shumkovska, B Ðošić-Markovska, D Zafirova-Roganović, ... Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za …, 2006 | 15 | 2006 |
| Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism N Zdraveska, V Anastasovska, M Kocova Journal of Pediatric Endocrinology and Metabolism 29 (7), 795-800, 2016 | 13 | 2016 |
| Newborn screening for thyroid-stimulating hormone as an indicator for assessment of iodine status in the Republic of Macedonia V Anastasovska, M Kocova Journal of Medical Biochemistry 35 (4), 385, 2016 | 12 | 2016 |
| Direct molecular diagnosis of CYP21A2 point mutations in Macedonian and Serbian patients with 21-hydroxylase deficiency V Anastasovska, T Milenković, M Kocova Journal of Medical Biochemistry 34 (1), 52, 2014 | 9 | 2014 |
| The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family M Kocova, V Anastasovska, I Bitovska European Journal of Medical Research 24, 1-6, 2019 | 8 | 2019 |
| Regional variation in the incidence of congenital hypothyroidism in Macedonia V Anastasovska, E Sukarova-Angelovska, M Pesevska, E Taseva, ... International Journal of Neonatal Screening 3 (3), 22, 2017 | 7 | 2017 |
| Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood M Kocova, N Zdraveska, M Zdravkovska, V Anastasovska, ... SAGE open medical case reports 4, 2050313X16683623, 2016 | 7 | 2016 |
| Impact of lower screening TSH cutoff level on the increasing prevalence of congenital hypothyroidism V Anastasovska, M Kocova International Journal of Neonatal Screening 3 (2), 7, 2017 | 6 | 2017 |
| Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in macedonian patients with congenital adrenal hyperplasia and their relatives. V Anastasovska, M Kocova Contributions of Macedonian Academy of Sciences & Arts 31 (2), 2010 | 6 | 2010 |
