Anastasovska, Violeta
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Anastasovska, Violeta
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Results 21-40 of 77 (Search time: 0.016 seconds).
| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 21 | Difficulties in diagnosing variable disorders of sexual development | Shukarova Angelovska, Elena ; Krstevska Konstantinova, Marina ; Alulovska, Natasha; Ilieva, Gordana; Anastasovska, Violeta | 19-Sep-2019 | Proceeding article | |
| 22 | 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 | |
| 23 | Duplication of 10q22.2q23.1 as a cause for severe hypotonia in a child | Ilieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Naunova Timovska, Silvana ; Pesevska, Milica; Anastasovska, Violeta | 6-Jun-2020 | Proceeding article | |
| 24 | Early onset of complex seizures as a first sign of 16p11.2 deletion syndrome | Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan | 6-Jun-2020 | Proceeding article | |
| 25 | Effects of different dietary fatty acid supplements upon lipoprotein metabolism and lipid peroxides production in hyperlipidemic rats. | Dimitrova Shumkovska, Jasmina ; Ðošić-Markovska, Bozidarka; Zafirova-Roganović, Danica; Anastasovska, Violeta | 2006 | Article | |
| 26 | 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 | |
| 27 | 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 | |
| 28 | Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia | Violeta Anastasovska ; Mirjana Kocova | 1-Apr-2017 | Article | |
| 29 | Evaluation of selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article | |
| 30 | 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 | |
| 31 | 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 | |
| 32 | Frequency of detected genotypes in patients with salt-wasting form of 21-hydroxylase deficiency | Kochova, Mirjana ; Anastasovska, Violeta | 17-Apr-2019 | Proceeding article | |
| 33 | 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 | |
| 34 | Gender difference in leptin and adiponectin production in obese children | M. Tanaskoska; M. Kocova; V. Anastasovska ; S. Kuzmanovska | Jun-2014 | Proceeding article | |
| 35 | Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia | Nikolina Zdraveska ; Mirjana Kocova ; Nicholas, Adeline K; Violeta Anastasovska ; Schoenmakers, Nadia | 2020 | Article | |
| 36 |  | Genetics of transient congenital hypothyroidism | Zdraveska, Nikolina ; Anastasovska, Violeta ; Kocova Mirjana | 11-Jun-2022 | Proceeding article |
| 37 | 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 | |
| 38 | Genotype-phenotype correlation in CAH patients with severe CYP21A2 point mutations in the Republic of Macedonia | Violeta Anastasovska ; Mirjana Kocova | Sep-2010 | Article | |
| 39 | High incidence of congenital hypothyroidism in one region of the Republic of Macedonia | V Anastasovska ; R Koviloska; M Kocova | Jun-2014 | Article | |
| 40 | The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family | Mirjana Kocova ; Violeta Anastasovska ; Iskra Bitovska | 19-Jun-2019 | Article |