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Kochova, Mirjana

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Full Name
Kochova, Mirjana
Vernacular Name
Мирјана Кочова
 
Variants
Kocova Mirjana
Kocova M
M Kocova
Mirjana Kochova
Мирјана Кочова
 
Main Affiliation
 
Email
mirjana.kochova@medf.ukim.edu.mk
 
Other emails
 
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Publications

Refined By:
Date Issued:  [2010 TO 2019]
Date Issued:  2015

Results 1-7 of 7 (Search time: 0.013 seconds).

PreviewTitleAuthor(s)Issue DateType
1Clinical 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
2Comments on 'Newborn screening in southeastern Europe' published in Molecular Genetics and Metabolism, 2014 Sept-Oct;113(1-2):42-45 by U. Groselj, M. ZerjavTansek, A. Smon, N. Angelkova, D. Anton, I. Baric, M. Djordjevic, L. Grimci, M. Ivanova, A. Kadam, V. Mulliqi Kotori, H. Maksic, O. Marginean, O. Margineanu, O. Milijanovic, F. Moldovanu, M. Muresan, S. Murko, M. Nanu, B. Repic Lampert, M. Samardzic, V. Sarnavka, A. Savov, M. Stojiljkovic, B. Suzic, R. Tincheva, H. Tahirovic, A. Toromanovic, N. Usurela, T. BattelinoMirjana Kocova ; Violeta Anastasovska Dec-2015Article
3Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase DeficiencyAnastasovska Violeta ; Milenković Tatjana ; Kocova Mirjana Jan-2015Article
4Metabolic Setup and Risks in Obese ChildrenKocova Mirjana ; Sukarova-Angelovska Elena ; Tanaskoska Milica; Palcevska-Kocevska Snezana; Krstevska MarijaJan-2015Article
5Optic 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
6Seasonal variation in month of diagnosis in children with type 1 diabetes registered in 23 European centers during 1989-2008: little short-term influence of sunshine hours or average temperaturePatterson, C C; Gyürüs, E; Rosenbauer, J; Cinek, O; Neu, A; Schober, E; Parslow, R C; Joner, G; Svensson, J; Castell, C; Bingley, P J; Schoenle, E; Jarosz-Chobot, P; Urbonaité, B; Rothe, U; Kržišnik, C; Ionescu-Tirgoviste, C; Weets, I; Kocova, M ; Stipancic, G; Samardzic, M; de Beaufort, C E; Green, A; Soltész, G; Dahlquist, G GDec-2015Article
7Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated?Sukarova Angelovska, E ; Kocova, M ; Zorcec, T 2015Proceeding article