Browsing by Author Shukarova Angelovska, Elena
Showing results 31 to 50 of 53
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| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| The many faces of oral-facial-digital syndrome | E Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova | Jun-2012 | Article | |
| Metabolic Setup and Risks in Obese Children | Kocova Mirjana ; Sukarova-Angelovska Elena ; Tanaskoska Milica; Palcevska-Kocevska Snezana; Krstevska Marija | Jan-2015 | Article | |
| Methodological and organizational aspects of newborn screening for congenital hypothyroidism in Macedonia | Gjurkova, Beti; Anastasovska, Violeta ; Sukarova-Angelovska, Elena ; Kocova, Mirjana | Jul-2008 | Article | |
| Missense variant contribution to USP9X-female syndrome | Jolly 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 Jozef | 2020 | Article | |
| MUTATION ANALYSIS OF THE COMMON DEAFNESS GENES IN PATIENTS WITH NONSYNDROMIC HEARING LOSS IN REPUBLIC OF MACEDONIA | Shukarova Stefanovska Emilija; Bozhinovski, GJorgji ; Momirovska Ana; Davcheva Chakar, Marina ; Shukarova Angelovska, Elena ; Plasheska-Karanfilska Dijana | 2017 | Article | |
| A need for a follow up od children with Williams syndrom | Sukarova Angelovska, E ; Kocova, M ; Kacarska, R ; Krstevska-Konstantinova, M; Nikolovska, N; Sahpazova, E; Zorcec, T | 2007 | Proceeding article | |
| New Vascular Anomaly in a Girl With Turner Syndrome: Mid-Aortic Narrowing | Mirjana Kocova ; Rozana Kacarska ; Elena Sukarova-Angelovska ; Dafina Kuzmanovska | 2012 | Article | |
| Optic glioma and precocious puberty in a girl with neurofibromatosis type 1 carrying an R681X mutation of NF1: case report and review of the literature | Mirjana Kocova ; Elena Kochova; Elena Sukarova-Angelovska | 15-Dec-2015 | Article | |
| Paediatric patient with deletion on chromosome 10q11.22 diagnosed by aCGH | Pesevska, Milica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Ilieva, Gordana | 6-Jun-2020 | Proceeding article | |
| Phenotypic variations in Wolf-Hirschhorn syndrome | E Sukarova-Angelovska ; M Kocova ; V Sabolich; S Palcevska; N Angelkova | Jun-2014 | Article | |
| Pituitary pseudotumor with unusual presentation reversed shortly after the introduction of thyroxine replacement therapy | M. Kocova ; S. Netkov; E. Sukarova-Angelovska | 2001 | Article | |
| Premature thelarche in Macedonia: a three-year follow-up | Krstevska-Konstantinova M ; Kocova M ; Gucev Z ; Sukarova-Angelovska E | 2007 | Article | |
| Prenatal Diagnosis of Cryptic Translocation t(5p;17q) with Fluorescent In Situ Hybridization | E. Sukarova-Angelovska ; M. Kocova ; E. Sukarova-Stefanovska; G. Ilieva; T. Hristova-Dimkovska; S. Kostadinova-Kunovska | 8-Mar-2018 | Article | |
| Rare case of Killian-Pallister syndrome associated with idiopathic short stature detected with fluorescent in situ hybridization on buccal smear | Elena Sukarova-Angelovska ; Mirjana Kocova ; Gordana Ilieva; Natalija Angelkova; Elena Kochova | 2016 | Article | |
| Regional Variation in the Incidence of Congenital Hypothyroidism in Macedonia | Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Pesevska; Elizabeta Taseva; Mirjana Kocova | 21-Aug-2017 | Article | |
| Remission phase of type 1 diabetes in children in the Republic of Macedonia | Kocova, Mirjana J ; Sukarova-Angelova, Elena P ; Krstevska-Konstantinova, Marina M | Sep-2000 | Proceeding article | |
| Seven years experience with selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kocova Mirjana ; Shukarova Angelovska, Elena ; Pesevska, Milica; Zdraveska, Nikolina | 10-Nov-2021 | Proceeding article | |
| Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated? | Sukarova Angelovska, E ; Kocova, M ; Zorcec, T | 2015 | Proceeding article | |
| Two cases of non-syndromic congenital unilateral breast hypoplasia in one family | Marina Krstevska-Konstantinova ; Konstandina Kuzevska-Maneva ; Elena Sukarova-Angelovska ; Ana Stamatova; Velibor Tasic ; Zoran Gucev ; Julia Haefele | 20-Feb-2020 | Article | |
| The unique combination of dermatological and ocular phenotypes in Alström syndrome: severe presentation, early onset and two novel ALMS1 mutations | M. Kocova ; E. Sukarova-Angelovska ; R. Kacarska ; P. Maffei; G. Milan; J.D. Marshall | Apr-2011 | Article |