Shukarova Angelovska, Elena
Full Name
Shukarova Angelovska, Elena
Main Affiliation
Email
elena.shukarova.angelovska@medf.ukim.edu.mk
Loading...
2
0
5
0
false
Loading...
3
0
5
0
false
Publications
(Articles)
Date issued
Type
Results 1-20 of 32 (Search time: 0.035 seconds).
| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 1 | 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 | |
| 2 | 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 | |
| 3 | 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 | |
| 4 | 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 | |
| 5 | Demographic, Clinical and Biochemical Characteristics of Pediatric Obesity: Interim Analysis of a Larger Prospective Study | Tankoska Maja; Jakimovski, Dejan ; Stamatova Ana; Murtezani Avni; Maneva Elita; Shukarova Angelovska, Elena ; Gjurkova-Angelovska Beti; Kocheva, Svetlana ; Kuzevska-Maneva, Konstandina ; Krstevska Konstantinova, Marina | Dec-2020 | Article | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | DETECTION OF A RARE MUTATION IN A NOONAN SYNDROME SUSPECTED PATIENT: A CASE REPORT | Dobrevski, Boban ; Shukarova Angelovska, Elena ; Kirijas, Meri ; Milanovski Gorjan; Brnjarchevska, Teodora ; Boceska Frosina; Petlichkovski, Aleksandar | Apr-2020 | Article | |
| 9 | 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 | |
| 10 | 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 | |
| 11 | 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 | |
| 12 | 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 | |
| 13 | 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 | |
| 14 | 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 | |
| 15 | 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 | |
| 16 | DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILY | Pop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena | 2021 | Article | |
| 17 | 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 | |
| 18 | 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 | |
| 19 | Growing Prevalence and Incidence of Diabetes in Republic of Macedonia in past 5 years based on data from the national system for electronic health records | Ahmeti, Irfan ; Bitoska, Iskra ; Markovikj, Snezhana ; Shukarova Angelovska, Elena ; Jovanovska Mishevska, Sasha ; Kochinski, Goran | Sep-2020 | Article | |
| 20 | Implementation of Novel Mode for Evaluation of MYCN Amplification that can Predict Outcome in Patients with Neuroblastoma | Ilieva Gordana; Kocova Mirjana ; Conevska Biljana; Shukarova Angelovska, Elena | 2020 | Article |