Browsing by Author Shukarova Angelovska, Elena
Showing results 7 to 26 of 53
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| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| 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 | |
| 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 | |
| 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 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILY | Pop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena | 2021 | Article | |
| 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 | |
| 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 | |
| Genetics in Macedonia-Following the international trends | Elena Sukarova-Angelovska ; Aleksandar Petlichkovski | 2018 | 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 | |
| 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 | |
| HLA-DR-DQ haplotypes and type 1 diabetes in Macedonia | Ilonen, Jorma; Kocova, Mirjana ; Lipponen, Kati; Sukarova-Angelovska, Elena ; Jovanovska, Aleksandra; Knip, Mikael | Jun-2009 | Article | |
| Implementation of Fluorescent in situ hybridization (FISH) as a method for detecting microdeletion syndromes - our first experiences | Sukarova-Angelovska E. ; Piperkova K.; Sredovska A.; Ilieva G.; Kocova M. | Dec-2007 | Article |