Full Name
Shukarova Angelovska, Elena
Main Affiliation
 
Email
elena.shukarova.angelovska@medf.ukim.edu.mk
 
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Publications
(Articles)

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Type:  Article

Results 1-20 of 31 (Search time: 0.021 seconds).

PreviewTitleAuthor(s)Issue DateType
1Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic countryMirjana Kocova ; Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Tanaskoska; Elizabeta TasevaApr-2015Article
2Correlation of serum adiponectin and leptin concentrations with anthropometric parameters in newbornsPalcevska-Kocevska, Snezana; Aluloska, Natasa; Krstevska, Marija ; Shukarova-Angelovska, Elena ; Kojik, Ljiljana; Zisovska, Elizabeta; Kocevski, Dragoslav ; Kocova, Mirjana 2012Article
3Demographic, Clinical and Biochemical Characteristics of Pediatric Obesity: Interim Analysis of a Larger Prospective StudyTankoska Maja; Jakimovski, Dejan ; Stamatova Ana; Murtezani Avni; Maneva Elita; Shukarova Angelovska, Elena ; Gjurkova-Angelovska Beti; Kocheva, Svetlana ; Kuzevska-Maneva, Konstandina ; Krstevska Konstantinova, Marina Dec-2020Article
4DETECTION OF A RARE MUTATION IN A NOONAN SYNDROME SUSPECTED PATIENT: A CASE REPORTDobrevski, Boban ; Shukarova Angelovska, Elena ; Kirijas, Meri ; Milanovski Gorjan; Brnjarchevska, Teodora ; Boceska Frosina; Petlichkovski, Aleksandar Apr-2020Article
5Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana 2018Article
6Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kochova, Mirjana Feb-2018Article
7DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILYPop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena 2021Article
8Dysphagia as an early presentation of Di George's Syndrome- case reportPalchevska, Snezana; Gjurkova, Beti; Shukarova, Elena ; Stavrikj, Katarina ; Jovanovska, Jana; Aluloska, Natasha28-Feb-2021Article
9Genetics in Macedonia-Following the international trendsElena Sukarova-Angelovska ; Aleksandar Petlichkovski 2018Article
10Growing 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
11HLA-DR-DQ haplotypes and type 1 diabetes in MacedoniaIlonen, Jorma; Kocova, Mirjana ; Lipponen, Kati; Sukarova-Angelovska, Elena ; Jovanovska, Aleksandra; Knip, MikaelJun-2009Article
12Implementation 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
13Implementation 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
14IMPORTANCE 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
15The many faces of oral-facial-digital syndromeE Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova Jun-2012Article
16Metabolic Setup and Risks in Obese ChildrenKocova Mirjana ; Sukarova-Angelovska Elena ; Tanaskoska Milica; Palcevska-Kocevska Snezana; Krstevska MarijaJan-2015Article
17Methodological and organizational aspects of newborn screening for congenital hypothyroidism in MacedoniaGjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana Jul-2008Article
18Missense 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
19MUTATION 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
20New Vascular Anomaly in a Girl With Turner Syndrome: Mid-Aortic NarrowingMirjana Kocova ; Rozana Kacarska ; Elena Sukarova-Angelovska ; Dafina Kuzmanovska2012Article