Browsing by Author Anastasovska, Violeta
Showing results 1 to 80 of 80
| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| 46, XX DSD with diphallus as a part of a multimalformative syndrome - a case report | Shukarova Angelovska, Elena ; Kochova, Mirjana ; Ilieva, Gordana; Anastasovska, Violeta ; Krstevska Konstantinova, Marina ; Filev, G | 23-Feb-2018 | Proceeding article | |
| BASELINE AND ACTH-STIMULATED SERUM 17-HYDROXYPROGESTERONE VALUES IN MACEDONIAN AND SERBIAN 21-HYDROXYLASE DEFICIENCY PATIENTS | V. Anastasovska ; M. Kocova; M. Tanaskoska; S. Kuzmanovska | 2014 | Proceeding article | |
| Chromosomal abnormalities in couples that undergo assisted reproduction technologies | Shukarova Angelovska, Elena ; Ilieva, Gordana; Anastasovska, Violeta ; Hristova-Dimkovska, Tanja; Nestoroska, Dragica | 17-Apr-2019 | Proceeding article | |
| Clinical and genomic characterization of 7q31.1 microduplication in a patient with developmental and neurological disabilities | Nestoroska, D; Anastasovska, V ; Shukarova Angelovska, E ; Pesevska, M; Veseli, A; Ilieva, G | 28-Aug-2021 | Proceeding article | |
| Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency | Mirjana Kochova ; Violeta Anastasovska ; Henrik Falhammar | 2020 | Article | |
| 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 | |
| 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 | |
| Coverage with Neonatal Thyroid Screening in the Republic of North Macedonia, during 2002–2020 | Pesevska, Milica; Anastasovska, Violeta ; Kocova, Mirjana ; Sukarova-Angelovska, Elena ; Fakovic, Nermina | 10-Nov-2021 | Proceeding article | |
| Detected genotypes in Macedonian patients with simple virilizing form of congenital adrenal hyperplasia | Anastasovska, Violeta ; Kochova, Mirjana ; Shukarova Angelovska, Elena ; Zdraveska, Nikolina ; Ilieva, Gordana | 17-Apr-2019 | Proceeding article | |
| 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 | |
| Detection of 3p25 microdeletion syndrome in the Macedonian patient with significant psychomotor retardation | Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica; Stojanova, Ivana | 28-Aug-2021 | Proceeding article | |
| Detection of giant chromosomal material on 7p+ with conventional karyotyping and aCGH | Ilieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Muaremoska-Kanzoska, Ljelja; Pesevska, Milica; Anastasovska, Violeta | 28-Aug-2021 | Proceeding article | |
| Detection of the pathogenic CNVs in the Macedonian patient with profound developmental delay | Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Zdraveska, Nikolina ; Ilieva, Gordana; Pesevska, Milica | 6-Jun-2020 | Proceeding article | |
| 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 | |
| Determination of monosomy 17 in anemia aplastica using fluorescence in situ hybridization | Ilieva, Gordana; Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Koceva, Svetlana | 17-Apr-2019 | Proceeding article | |
| Development delay in paediatric patient with deletion on chromosome 15q26.2 | Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana; Panovska, Sandra | 28-Aug-2021 | Proceeding article | |
| Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism | Zdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana | 2018 | Article | |
| 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 | |
| The Diagnostic Value of Anti-Cyclic Citrullinated Peptide Antibodies (anti-CCP) in Patients with Rheumatoid Arthritis | Damjanovska, LJubinka ; Anastasovska, Violeta ; Gruev, Todor | 1-Dec-2007 | Article | |
| Different ethnical distribution of the incidence of cystic fibrosis in Republic of North Macedonia | Anastasovska, Violeta ; Fushtikj, Stojka ; Pesevska, Milica; Fakovic, Nermina; Stamatova, Ana | 9-Jun-2021 | Proceeding article | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| Methodological and organizational aspects of newborn screening for congenital hypothyroidism in Macedonia | Gjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana | Jul-2008 | Article | |
| Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy | Anastasovska, V ; Kocova, M | 1-Jan-2007 | Article | |
| Molecular detection of Herpes simplex virus type 1, Herpes simplex virus type 2, Cytomegalovirus and Epstein-barr virus in subgingival dental plaque in patients with periodontal disease | Ivanovska-Stojanovska, Marija; Popovska, Mirjana ; Anastasovska, Violeta ; Kochova, Mirjana ; Zendeli Bedjeti, Lindita; Atanasovska-Stojanovska, Aneta; Todorovska, Sashka | 17-Apr-2019 | Proceeding article | |
| Molecular detection of virus herpes simplex type 1 (HSV-1), virus herpes simplex type 2 (HSV-2), Cytomegalovirus (HCMV) and Epstein-barr virus (EBV) in supra-gingival dental plaque in patients with periodontal disease. | Ivanovska-Stojanoska, Marija; Popovska, Mirjana ; Anastasovska, Violeta ; Zendeli-Bedjeti, Lindita; Todorovska, Sashka | Dec-2018 | Article | |
| Molecular diagnosis of MCAD in the Macedonian neonates with elevated medium-chain acylcarnitines identified through MS/MS-based newborn screening | Anastasovska, Violeta ; Kocova, Mirjana ; Zdraveska, Nikolina ; Tesovnik, Tine; Debeljak, Maruša; Kovač, Jernej | 2022 | Proceeding article | |
| Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiency | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article | |
| Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of Macedonia | Anastasovska Violeta ; Kocova Mirjana | Oct-2016 | Article | |
| A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia | Violeta Anastasovska ; Mirjana Kocova ; Nikolina Zdraveska ; Maja Stojiljkovic; Anita Skakic; Kristel Klaassen; Sonja Pavlovic | 14-Mar-2021 | Article | |
| A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia | Anastasovska, V ; Kocova, E; Kocova, M | 1-Jan-2010 | Article | |
| Paediatric patient with deletion on chromosome 10q11.22 diagnosed by aCGH | Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana | 6-Jun-2020 | Proceeding article | |
| Phenylketonuria screening in the Republic of Macedonia | Mirjana Kocova ; Violeta Anastasovska | 2016 | Article | |
| Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years | Anastasovska, Violeta ; Pesevska, Milica; Zdraveska, Nikolina ; Zafirova, Biljana ; Meceska Jovcevska, Jasmina; Kochova, Mirjana | 2023 | Article | |
| Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years | Anastasovska, Violeta ; Peshevska, Milica; Zdraveska, Nikolina ; Zafirova, Biljana ; Jovcevska Meceska, Jasmina; Kochova, Mirjana | 2023 | Article | |
| Rano otkrivanje urođenih grešaka metabolizma neonatalnim skriningom – slučaj sa poremećajem u metabolizmu masnih kiselina srednjih lanaca | Zlateska, Snezana; Anastasovska, Violeta ; Zlateska, Sofija; Zlateska, A | 20-Sep-2018 | Proceeding article | |
| Regional Variation in the Incidence of Congenital Hypothyroidism in Macedonia | Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Pesevska; Elizabeta Taseva; Mirjana Kocova | 21-Aug-2017 | Article | |
| Results from a newborn screening (NBS) pilot study for cystic fibrosis in the Republic of Macedonia. | Fustik, Stojka; Anastasovska, Violeta ; Plasheska Karanfilska, Dijana; Spirevska, Lidija; Stamatova, Ana; Pesevska, Milica; Terzic, Marija | 5-Jun-2019 | Proceeding article | |
| Seven years experience with selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kocova Mirjana ; Shukarova Angelovska, Elena ; Pesevska, Milica; Zdraveska, Nikolina | 10-Nov-2021 | Proceeding article | |
 | The spectrum of CFTR mutations in newly diagnosed cases of cystic fibrosis through newborn screening in the Republic of North Macedonia | Fustik, Stojka ; Anastasovska, Violeta ; Plaseska Karanfilska, Dijana; Stamatova, Ana; Spirevska, Lidija; Pesevska, Milica; Terzikj, Marija; Vujovic, Marija | Jun-2022 | Proceeding article |
| Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood | Mirjana Kocova ; Nikolina Zdraveska ; Maja Zdravkovska ; Violeta Anastasovska ; Daniela Pop Gjorceva | 2016 | Article | |
| Targeted sequencing of dyshormonogenesis-associated genes in Macedonian cases with congenital hypothyroidism and gland-in-situ reveals a low mutation frequency | Zdraveska, Nikolina ; Kocova, Mirjana ; Nicholas, Adeline K; Anastasovska, Violeta ; Schoenmakers, Nadia | 2-Nov-2018 | Proceeding article | |
| Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-up | Mirjana Kocova ; Vesna Janevska ; Violeta Anastasovska | Apr-2018 | Article | |
| Therapeutic challenges in a patient with the simple virilizing (SV) form of congenital adrenal hyperplasia (CAH) due to the P30L/I172N genotype | Maja Tankoska; Violeta Anastasovska ; Marina Krstevska-Konstantinova ; Michel Naydenov; Mirjana Kocova | 27-May-2019 | Article | |
| Thyroid peroxidase (TPO) mutations in Macedonian patients with congenital hypothyroidism | Zdraveska, Nikolina ; Anastasovska, Violeta ; Schoenmakers, Nadia; Nicholas, K. Adeline; Kochova, Mirjana | 6-Jun-2020 | Proceeding article | |
| Transient congenital hypothyroidism in preterm and full-term infants | Zdraveska, Nikolina ; Anastasovska, Violeta ; Kochova, Mirjana | 9-Jun-2019 | Proceeding article | |
| Two Years of Newborn Screening for Cystic Fibrosis in North Macedonia: First Experience | Fustik S ; Anastasovska V ; Plaseska-Karanfilska D; Stamatova A; Spirevska L; Pesevska M; Terzikj M; Vujovic M | Jul-2021 | Article | |
| Two-year neonatal screening for cystic fibrosis in Republic of North Macedonia | Fustik, Stojka; Anastasovska, Violeta ; Plaseska-Karanfilska, Dijana; Stamatova, Ana; Spirevska, Lidija; Pesevska, Milica; Terzic, Marija; Fakovic, Nermina | 9-Jun-2021 | Proceeding article | |
| Variations in incidence of congenital hypothyroidism in association with changes of cutoff value | Pesevska, Milica; Anastasovska, Violeta ; Taseva, Elizabeta; Zdraveska, Nikolina ; Gurzanova-Durnev, Liljana; Kochova, Mirjana | 3-Oct-2018 | Proceeding article | |
| Воведување на неонатален скрининг за хипотироидизам во Република Македонија | М. Кочова ; В. Анастасовска ; Е. Шукарова-Ангеловска ; Б. Ѓуркова; Е. Јовчева | 2002 | Article | |
| Квантитативно одредување на активноста на еритроцитната глукоза-6-фосфат дехидрогеназа кај деца со феродефицитна анемија | В. Анастасовска ; Б. Ѓошиќ-Марковска; О. Муратовска | 2005 | Article | |
| Клинички и молекуларни аспекти на конгенитална адренална хиперплазија (21-хидроксилаза дефицит) - Наши искуства | Виолета Анастасовска ; Мирјана Кочова | 2023 | Book | |
| Неонатален скрининг во Република Македонија | Мирјана Кочова ; Виолета Анастасовска | Dec-2018 | Article | |
| Неонатален скрининг за вроден хипотироидизам методолошки пристап | Бети Ѓуркова; Виолета Анастасовска ; Мирјана Кочова | 2007 | Article | |
| Современи методи во детекцијата на хромозомските аберации | Шукарова-Ангеловска, Елена ; Анастасовска, Виолета ; Нестороска, Драгица; Петровска, Емилија | 10-Nov-2020 | Proceeding article | |
| ЈОДЕН И ТИРОИДЕН СТАТУС НА НАСЕЛЕНИЕТО ВО МАКЕДОНИЈА | Anastasovska, Violeta ; Atanasova Boshku, Aleksandra ; Vaskova, Olivija ; Dimitrov, Goran ; Dimovski, Vladimir; Zdrvevska, Nikolina; Jovanovska, Viktorija ; Karanfilski, Borislav; Kochova, Mirjana ; Kochoski, Goran ; Kuzmanovska, Sonja ; Majstorov, Venjamin ; Miladinovska, Daniela; Kostova Milevska, Neda; Pop Gjorcheva, Daniela ; Samardjiski, Igor ; Stefanija, Adela; Ugrinska, Ana ; Chuleva, Biljana; Shabani, Ajla | 2018 | Book | |
| ЈОДЕН И ТИРОИДЕН СТАТУС НА НАСЕЛЕНИЕТО ВО МАКЕДОНИЈА: 2018 ГОДИНА | Каранфилски, Борислав; Атанасова Бошку, Александра ; Васкова, Оливија ; Димитров, Горан ; Димковски, Владимир; Здравеска, Николина ; Јовановска, Викторија; Анастасовска, Виолета ; Кочова, Мирјана ; Кочоски, Горан ; Кузмановска, Соња ; Мајсторов, Венјамин ; Миладинова, Даниела ; Милевска Костова, Неда; Поп Ѓорчева, Даниела ; Самарџиски, Игор; Стефанија, Адела; Угринска, Ана ; Чулева, Билјана | 2019 | Book chapter |