Browsing by Author Shukarova Angelovska, Elena
Showing results 16 to 35 of 53
< previous
next >
Preview | Title | Author(s) | Issue Date | Type |
---|---|---|---|---|
Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism | Zdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kochova, Mirjana | Feb-2018 | Article | |
Difficulties in diagnosing variable disorders of sexual development | Shukarova Angelovska, Elena ; Krstevska Konstantinova, Marina ; Alulovska, Natasha; Ilieva, Gordana; Anastasovska, Violeta | 19-Sep-2019 | Proceeding article | |
Duplication of 10q22.2q23.1 as a cause for severe hypotonia in a child | Ilieva, Gordana; Shukarova Angelovska, Elena ; Nestoroska, Dragica; Naunova Timovska, Silvana ; Pesevska, Milica; Anastasovska, Violeta | 6-Jun-2020 | Proceeding article | |
DUPLICATION OF CHROMOSOME 16p13.11-p12.3 WITH DIFFERENT EXPRESSIONS IN THE SAME FAMILY | Pop-Jordanova Nada; Zorcec, Tatjana ; Shukarova Angelovska, Elena | 2021 | Article | |
Dysphagia as an early presentation of Di George's Syndrome- case report | Palchevska, Snezana; Gjurkova, Beti; Shukarova, Elena ; Stavrikj, Katarina ; Jovanovska, Jana; Aluloska, Natasha | 28-Feb-2021 | Article | |
Early onset of complex seizures as a first sign of 16p11.2 deletion syndrome | Shukarova Angelovska, Elena ; Anastasovska, Violeta ; Duma, Filip ; Muaremovska, Ljelja; Nestoroska, Dragica; Ilieva, Gordana; Pesevska, Milica; Velkov, Milan | 6-Jun-2020 | Proceeding article | |
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 |