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

Refined By:
Date Issued:  [2010 TO 2019]
Fulltext:  With Fulltext

Results 1-10 of 10 (Search time: 0.017 seconds).

PreviewTitleAuthor(s)Issue DateType
146, XX DSD with diphallus as a part of a multimalformative syndrome - a case reportShukarova Angelovska, Elena ; Kochova, Mirjana ; Ilieva, Gordana; Anastasovska, Violeta ; Krstevska Konstantinova, Marina ; Filev, G23-Feb-2018Proceeding article
2Chromosomal abnormalities in couples that undergo assisted reproduction technologiesShukarova Angelovska, Elena ; Ilieva, Gordana; Anastasovska, Violeta ; Hristova-Dimkovska, Tanja; Nestoroska, Dragica17-Apr-2019Proceeding article
3Detected genotypes in Macedonian patients with simple virilizing form of congenital adrenal hyperplasiaAnastasovska, Violeta ; Kochova, Mirjana ; Shukarova Angelovska, Elena ; Zdraveska, Nikolina ; Ilieva, Gordana17-Apr-2019Proceeding article
4Determination of monosomy 17 in anemia aplastica using fluorescence in situ hybridizationIlieva, Gordana; Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Koceva, Svetlana17-Apr-2019Proceeding article
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
6Difficulties in diagnosing variable disorders of sexual developmentShukarova Angelovska, Elena ; Krstevska Konstantinova, Marina ; Alulovska, Natasha; Ilieva, Gordana; Anastasovska, Violeta 19-Sep-2019Proceeding article
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
8Late diagnosis of phenylketonuria-time for changesNatalija Angelkova; Vesna Sabolic; Elena Sukarova Angelkovska ; Tatjana Zorchec ; Elena Kochova; Filip Duma 2015Proceeding article
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
10Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated?Sukarova Angelovska, E ; Kocova, M ; Zorcec, T 2015Proceeding article