Browsing by Author Shukarova Angelovska, Elena
Showing results 22 to 41 of 53
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| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| Genetics in Macedonia-Following the international trends | Elena Sukarova-Angelovska ; Aleksandar Petlichkovski | 2018 | Article | |
| Genomic and clinical characterisation of microduplications in a patient with developmental delay | Nestoroska, Dragica; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Pesevska, Milica; Ilieva, Gordana | 6-Jun-2020 | Proceeding article | |
| Growing Prevalence and Incidence of Diabetes in Republic of Macedonia in past 5 years based on data from the national system for electronic health records | Ahmeti, Irfan ; Bitoska, Iskra ; Markovikj, Snezhana ; Shukarova Angelovska, Elena ; Jovanovska Mishevska, Sasha ; Kochinski, Goran | Sep-2020 | Article | |
| HLA-DR-DQ haplotypes and type 1 diabetes in Macedonia | Ilonen, Jorma; Kocova, Mirjana ; Lipponen, Kati; Sukarova-Angelovska, Elena ; Jovanovska, Aleksandra; Knip, Mikael | Jun-2009 | Article | |
| Implementation of Fluorescent in situ hybridization (FISH) as a method for detecting microdeletion syndromes - our first experiences | Sukarova-Angelovska E. ; Piperkova K.; Sredovska A.; Ilieva G.; Kocova M. | Dec-2007 | Article | |
| Implementation of Novel Mode for Evaluation of MYCN Amplification that can Predict Outcome in Patients with Neuroblastoma | Ilieva Gordana; Kocova Mirjana ; Conevska Biljana; Shukarova Angelovska, Elena | 2020 | Article | |
| IMPORTANCE OF 6-MINUTE WALK TEST IN DIAGNOSTICS OF RARE METABOLIC MYOPATHY - A CASE REPORT OF CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY | Angelkova Natalija; Shukarova Angelovska, Elena ; Kocova Mirjana ; Duma, Filip ; Sabolich Vesna; Mandjukovska Hristina | Dec-2017 | Article | |
| Incidence of Congenital Hypothyroidism in the Republic of North Macedonia in Correlation with TSH Cutoff Level | Anastasovska, Violeta ; Pesevska, Milica; Kocova, Mirjana ; Shukarova Angelovska, Elena ; Fakovic, Nermina; Karishik, Senada | 10-Nov-2021 | Proceeding article | |
| Late diagnosis of phenylketonuria-time for changes | Natalija Angelkova; Vesna Sabolic; Elena Sukarova Angelkovska ; Tatjana Zorchec ; Elena Kochova; Filip Duma | 2015 | Proceeding article | |
| 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 |