Full Name
Shukarova Angelovska, Elena
Main Affiliation
 
Email
elena.shukarova.angelovska@medf.ukim.edu.mk
 
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Publications
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Results 1-11 of 11 (Search time: 0.016 seconds).

PreviewTitleAuthor(s)Issue DateType
1Demographic, 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
2DETECTION 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
3Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana 2018Article
4DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILYPop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena 2021Article
5Growing 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
6Implementation 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
7IMPORTANCE 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
8Missense 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
9MUTATION 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
10Premature thelarche in Macedonia: a three-year follow-upKrstevska-Konstantinova M ; Kocova M ; Gucev Z ; Sukarova-Angelovska E 2007Article
11Воведување на неонатален скрининг за хипотироидизам во Република МакедонијаМ. Кочова ; В. Анастасовска ; Е. Шукарова-Ангеловска ; Б. Ѓуркова; Е. Јовчева2002Article