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Browsing by Author Shukarova Angelovska, Elena


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Showing results 18 to 37 of 53 < previous   next >
PreviewTitleAuthor(s)Issue DateType
Duplication of 10q22.2q23.1 as a cause for severe hypotonia in a childIlieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Naunova Timovska, Silvana ; Pesevska, Milica; Anastasovska, Violeta 6-Jun-2020Proceeding article
DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILYPop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena 2021Article
Dysphagia as an early presentation of Di George's Syndrome- case reportPalchevska, Snezana; Gjurkova, Beti; Shukarova, Elena ; Stavrikj, Katarina ; Jovanovska, Jana; Aluloska, Natasha28-Feb-2021Article
Early onset of complex seizures as a first sign of 16p11.2 deletion syndromeShukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan6-Jun-2020Proceeding article
Genetics in Macedonia-Following the international trendsElena Sukarova-Angelovska ; Aleksandar Petlichkovski 2018Article
Genomic and clinical characterisation of microduplications in a patient with developmental delayNestoroska, Dragica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Pesevska, Milica; Ilieva, Gordana6-Jun-2020Proceeding 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 recordsAhmeti, Irfan ; Bitoska, Iskra ; Markovikj, Snezhana ; Shukarova Angelovska, Elena ; Jovanovska Mishevska, Sasha ; Kochinski, GoranSep-2020Article
HLA-DR-DQ haplotypes and type 1 diabetes in MacedoniaIlonen, Jorma; Kocova, Mirjana ; Lipponen, Kati; Sukarova-Angelovska, Elena ; Jovanovska, Aleksandra; Knip, MikaelJun-2009Article
Implementation of Fluorescent in situ hybridization (FISH) as a method for detecting microdeletion syndromes - our first experiencesSukarova-Angelovska E. ; Piperkova K.; Sredovska A.; Ilieva G.; Kocova M. Dec-2007Article
Implementation of Novel Mode for Evaluation of MYCN Amplification that can Predict Outcome in Patients with NeuroblastomaIlieva Gordana; Kocova Mirjana ; Conevska Biljana; Shukarova Angelovska, Elena 2020Article
IMPORTANCE OF 6-MINUTE WALK TEST IN DIAGNOSTICS OF RARE METABOLIC MYOPATHY - A CASE REPORT OF CARNITINE PALMITOYLTRANSFERASE II DEFICIENCYAngelkova Natalija; Shukarova Angelovska, Elena ; Kocova Mirjana ; Duma, Filip ; Sabolich Vesna; Mandjukovska HristinaDec-2017Article
Incidence of Congenital Hypothyroidism in the Republic of North Macedonia in Correlation with TSH Cutoff LevelAnastasovska, Violeta ; Pesevska, Milica; Kocova, Mirjana ; Shukarova Angelovska, Elena ; Fakovic, Nermina; Karishik, Senada10-Nov-2021Proceeding article
Late diagnosis of phenylketonuria-time for changesNatalija Angelkova; Vesna Sabolic; Elena Sukarova Angelkovska ; Tatjana Zorchec ; Elena Kochova; Filip Duma 2015Proceeding article
The many faces of oral-facial-digital syndromeE Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova Jun-2012Article
Metabolic Setup and Risks in Obese ChildrenKocova Mirjana ; Sukarova-Angelovska Elena ; Tanaskoska Milica; Palcevska-Kocevska Snezana; Krstevska MarijaJan-2015Article
Methodological and organizational aspects of newborn screening for congenital hypothyroidism in MacedoniaGjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana Jul-2008Article
Missense variant contribution to USP9X-female syndromeJolly 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 Jozef2020Article
MUTATION ANALYSIS OF THE COMMON DEAFNESS GENES IN PATIENTS WITH NONSYNDROMIC HEARING LOSS IN REPUBLIC OF MACEDONIAShukarova Stefanovska Emilija; Bozhinovski, GJorgji ; Momirovska Ana; Davcheva Chakar, Marina ; Shukarova Angelovska, Elena ; Plasheska-Karanfilska Dijana2017Article
A need for a follow up od children with Williams syndromSukarova Angelovska, E ; Kocova, M ; Kacarska, R ; Krstevska-Konstantinova, M; Nikolovska, N; Sahpazova, E; Zorcec, T 2007Proceeding article
New Vascular Anomaly in a Girl With Turner Syndrome: Mid-Aortic NarrowingMirjana Kocova ; Rozana Kacarska ; Elena Sukarova-Angelovska ; Dafina Kuzmanovska2012Article
Showing results 18 to 37 of 53 < previous   next >