Kochova, Mirjana
Full Name
Kochova, Mirjana
Vernacular Name
Мирјана Кочова
Variants
Kocova Mirjana
Kocova M
M Kocova
Mirjana Kochova
Мирјана Кочова
Kocova M
M Kocova
Mirjana Kochova
Мирјана Кочова
Main Affiliation
Email
mirjana.kochova@medf.ukim.edu.mk
Other emails
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5
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false
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3
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false
Type
Fulltext
Results 1-18 of 18 (Search time: 0.025 seconds).
| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 1 | 46, XX DSD with diphallus as a part of a multimalformative syndrome - a case report | Shukarova Angelovska, Elena ; Kochova, Mirjana ; Ilieva, Gordana; Anastasovska, Violeta ; Krstevska Konstantinova, Marina ; Filev, G | 23-Feb-2018 | Proceeding article | |
| 2 | Clinical practice: experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia - a multiethnic country | Mirjana Kocova ; Violeta Anastasovska ; Elena Sukarova-Angelovska ; Milica Tanaskoska; Elizabeta Taseva | Apr-2015 | Article | |
| 3 | Correlation of serum adiponectin and leptin concentrations with anthropometric parameters in newborns | Palcevska-Kocevska, Snezana; Aluloska, Natasa; Krstevska, Marija ; Shukarova-Angelovska, Elena ; Kojik, Ljiljana; Zisovska, Elizabeta; Kocevski, Dragoslav ; Kocova, Mirjana | 2012 | Article | |
| 4 | Detected genotypes in Macedonian patients with simple virilizing form of congenital adrenal hyperplasia | Anastasovska, Violeta ; Kochova, Mirjana ; Shukarova Angelovska, Elena ; Zdraveska, Nikolina ; Ilieva, Gordana | 17-Apr-2019 | Proceeding article | |
| 5 | Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism | Zdraveska, Nikolina ; Zdravkovska, Maja ; Anastasovska, Violeta ; Shukarova Angelovska, Elena ; Kocova Mirjana | 2018 | Article | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | The many faces of oral-facial-digital syndrome | E Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova | Jun-2012 | Article | |
| 9 | Metabolic Setup and Risks in Obese Children | Kocova Mirjana ; Sukarova-Angelovska Elena ; Tanaskoska Milica; Palcevska-Kocevska Snezana; Krstevska Marija | Jan-2015 | Article | |
| 10 | New Vascular Anomaly in a Girl With Turner Syndrome: Mid-Aortic Narrowing | Mirjana Kocova ; Rozana Kacarska ; Elena Sukarova-Angelovska ; Dafina Kuzmanovska | 2012 | Article | |
| 11 | 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 | |
| 12 | Phenotypic variations in Wolf-Hirschhorn syndrome | E Sukarova-Angelovska ; M Kocova ; V Sabolich; S Palcevska; N Angelkova | Jun-2014 | Article | |
| 13 | 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 | |
| 14 | 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 | |
| 15 | 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 | |
| 16 | Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated? | Sukarova Angelovska, E ; Kocova, M ; Zorcec, T | 2015 | Proceeding article | |
| 17 | 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 | |
| 18 | Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes | Mirjana Kocova ; Nikolina Zdraveska ; Elena Sukarova-Angelovska | 2011 | Article |