Showing results 26 to 45 of 79
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Preview | Title | Author(s) | Issue Date | Type |
| Effects of different dietary fatty acids supplements upon lipid peroxides production in rats tissues with different phospholipid composition | Dimitrova Šumkovska, Jasmina ; Ðošić-Markovska, Bozidarka; Smiljevska, Vesna; Anastasovska, Violeta | 2004 | Article |
| Erythrocyte glucose-6-phosphate dehydrogenase activity in laboratory rats treated with amoxiclav, lidaprim and 1-chloro-2,4-dinitrobenzen. Preliminary communication. | Anastasovska, Violeta ; Ðošić-Markovska, Božidarka; Stojkovski, Velimir ; Dimitrova Shumkovska, Jasmina | 2005 | Article |
| Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia | Violeta Anastasovska ; Mirjana Kocova | 1-Apr-2017 | Article |
| Evaluation of selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article |
| 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 |
| First results from national newborn screening program for cystic fibrosis in the Republic of North Macedonia | Fustikj, Stojka; Anastasovska, Violeta ; Plasheska-Karanfilska, Dijana; Spirevska, Lidija; Pesevska, Milica; Terzikj, Marija; Stamatova, Ana | 3-Jun-2020 | Proceeding article |
| Frequency of detected genotypes in patients with salt-wasting form of 21-hydroxylase deficiency | Kochova, Mirjana ; Anastasovska, Violeta | 17-Apr-2019 | Proceeding article |
| 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 |
| Gender difference in leptin and adiponectin production in obese children | M. Tanaskoska; M. Kocova; V. Anastasovska ; S. Kuzmanovska | Jun-2014 | Proceeding article |
| Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia | Nikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia | 2020 | Article |
| Genetics of transient congenital hypothyroidism | Zdraveska, Nikolina ; Anastasovska, Violeta ; Kocova Mirjana | 11-Jun-2022 | Proceeding article |
| Genomic and clinical characterisation of microduplications in a patient with developmental delay | Nestoroska, Dragica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Pesevska, Milica; Ilieva, Gordana | 6-Jun-2020 | Proceeding article |
| Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of Macedonia | Violeta Anastasovska ; Mirjana Kocova | Sep-2010 | Article |
| High incidence of congenital hypothyroidism in one region of the Republic of Macedonia | V Anastasovska ; R Koviloska; M Kocova | Jun-2014 | Article |
| The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family | Mirjana Kocova ; Violeta Anastasovska ; Iskra Bitovska | 19-Jun-2019 | Article |
| Impact of Lower Screening TSH Cutoff Level on the Increasing Prevalence of Congenital Hypothyroidism | Anastasovska, Violeta ; Kocova, Mirjana | 4-Apr-2017 | Article |
| Incidence of congenital hypothyroidism in different regions of Macedonia - sixteen years newborn thyroid screening | Anastasovska, Violeta ; Pesevska, Milica; Taseva, Elizabeta; Sukarova-Angelovska, Elena; Zdraveska, Nikolina ; Gurzanova-Durnev Ljiljana; Kochova, Mirjana | 3-Oct-2018 | Proceeding article |
| Incidence of Congenital Hypothyroidism in the Republic of North Macedonia in Correlation with TSH Cutoff Level | Anastasovska, Violeta ; Pesevska, Milica; Kocova, Mirjana ; Shukarova Angelovska, Elena ; Fakovic, Nermina; Karishik, Senada | 10-Nov-2021 | Proceeding article |
| Introduction of neonatal screening for cystic fibrosis in the Republic of North Macedonia | Anastasovska, Violeta ; Pesevska, Milica; Fustik, Stojka ; Stamatova, Ana | 10-Nov-2021 | Proceeding article |
| 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 |