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

Refined By:
Author:  M. Kocova

Results 1-20 of 30 (Search time: 0.019 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
2Clinical 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
3Correlation 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
4Coverage with Neonatal Thyroid Screening in the Republic of North Macedonia, during 2002–2020Pesevska, Milica; Anastasovska, Violeta ; Kocova, Mirjana ; Sukarova-Angelovska, Elena ; Fakovic, Nermina10-Nov-2021Proceeding article
5Detected 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
6Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidismZdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana 2018Article
7Diagnostic 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
8HLA-DR-DQ haplotypes and type 1 diabetes in MacedoniaIlonen, Jorma; Kocova, Mirjana ; Lipponen, Kati; Sukarova-Angelovska, Elena ; Jovanovska, Aleksandra; Knip, MikaelJun-2009Article
9Implementation 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
10Implementation 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
11IMPORTANCE 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
12Incidence 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
13The many faces of oral-facial-digital syndromeE Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova Jun-2012Article
14Metabolic Setup and Risks in Obese ChildrenKocova Mirjana ; Sukarova-Angelovska Elena ; Tanaskoska Milica; Palcevska-Kocevska Snezana; Krstevska MarijaJan-2015Article
15Methodological and organizational aspects of newborn screening for congenital hypothyroidism in MacedoniaGjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana Jul-2008Article
16A 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
17New Vascular Anomaly in a Girl With Turner Syndrome: Mid-Aortic NarrowingMirjana Kocova ; Rozana Kacarska ; Elena Sukarova-Angelovska ; Dafina Kuzmanovska2012Article
18Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literatureMirjana Kocova ; Elena Kochova; Elena Sukarova-Angelovska 15-Dec-2015Article
19Phenotypic variations in Wolf-Hirschhorn syndromeE Sukarova-Angelovska ; M Kocova ; V Sabolich; S Palcevska; N AngelkovaJun-2014Article
20Pituitary pseudotumor with unusual presentation reversed shortly after the introduction of thyroxine replacement therapyM. Kocova ; S. Netkov; E. Sukarova-Angelovska 2001Article