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)
Type
Fulltext
Results 1-20 of 21 (Search time: 0.017 seconds).
| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 1 | 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 | |
| 2 | 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 | |
| 3 | 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 | |
| 4 | 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 | |
| 5 | 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 | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | 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 | |
| 9 | 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 | |
| 10 | DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILY | Pop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena | 2021 | Article | |
| 11 | Dysphagia as an early presentation of Di George's Syndrome- case report | Palchevska, Snezana; Gjurkova, Beti; Shukarova, Elena ; Stavrikj, Katarina ; Jovanovska, Jana; Aluloska, Natasha | 28-Feb-2021 | Article | |
| 12 | 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 | |
| 13 | 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 | |
| 14 | 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 | |
| 15 | 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 | |
| 16 | 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 | |
| 17 | Missense variant contribution to USP9X-female syndrome | Jolly Lachlan; Parnell Euan; Gardner Alison E.; Corbett Mark A.; Pérez-Jurado Luis A.; Shaw Marie; Lesca Gaetan; Keegan Catherine; Schneider Michael C.; Griffin Emily; Maier Felicitas; Kiss Courtney; Guerin Andrea; Crosby Kathleen; Rosenbaum Kenneth; Tanpaiboon Pranoot; Whalen Sandra; Keren Boris; McCarrier Julie; Basel Donald; Sadedin Simon; White Susan M.; Delatycki Martin B.; Kleefstra Tjitske; Küry Sébastien; Brusco Alfredo; Shukarova Angelovska, Elena ; Trajkova Slavica; Yoon Sehoun; Wood Stephen A.; Piper Michael; Penzes Peter; Gecz Jozef | 2020 | Article | |
| 18 | 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 | |
| 19 | 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 | |
| 20 | Two cases of non-syndromic congenital unilateral breast hypoplasia in one family | Marina Krstevska-Konstantinova ; Konstandina Kuzevska-Maneva ; Elena Sukarova-Angelovska ; Ana Stamatova; Velibor Tasic ; Zoran Gucev ; Julia Haefele | 20-Feb-2020 | Article |