Browsing by Author Kochova, Mirjana
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Preview | Title | Author(s) | Issue Date | Type |
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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 | |
Clinical variability in two Macedonian families with Arterial tortuosity syndrome | M Kocova ; R Kacarska ; K Kuzevska-Maneva ; S Prijic; M Lazareska; C Dordoni; M Ritelli; M Colombi | 29-Oct-2018 | Article | |
A cold spot of IDDM incidence in Europe. Macedonia | Kocova, M ; Trucco, M; Konstantinova, M ; Dorman, J S | Sep-1993 | Article | |
Comment on Publications from OpT2mise Study | Tatjana Milenkovic ; Mirjana Kocova ; Brankica Krstevska; Gordana Pemovska ; Ivica Smokovski | 2016 | Article | |
Comments 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. Battelino | Mirjana Kocova ; Violeta Anastasovska | Dec-2015 | Article | |
Complete atrio-ventricular block in childhood | Zdraveva, M; Doneva, V; Kocova, M ; Sadikario, A | 1977 | Article | |
Continuing stability of center differences in pediatric diabetes care: do advances in diabetes treatment improve outcome? The Hvidoere Study Group on Childhood Diabetes | de Beaufort, Carine E; Swift, Peter G F; Skinner, Chas T; Aanstoot, Henk J; Aman, Jan; Cameron, Fergus; Martul, Pedro; Chiarelli, Francesco; Daneman, Dennis; Danne, Thomas; Dorchy, Harry; Hoey, Hilary; Kaprio, Eero A; Kaufman, Francine; Kocova, Mirjana ; Mortensen, Henrik B; Njølstad, Pal R; Phillip, Moshe; Robertson, Kenneth J; Schoenle, Eugen J; Urakami, Tatsuhiko; Vanelli, Maurizio | Sep-2007 | Article | |
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 | |
Coverage with Neonatal Thyroid Screening in the Republic of North Macedonia, during 2002–2020 | Pesevska, Milica; Anastasovska, Violeta ; Kocova, Mirjana ; Sukarova-Angelovska, Elena ; Fakovic, Nermina | 10-Nov-2021 | Proceeding article | |
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 | |
Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relatives | Anastasovska Violeta ; Kocova Mirjana | 2010 | Article | |
Detection of Virus Herpes Simplex Type 1 in Patients with Chronic Periodontal Disease | Marija Ivanovska-Stojanoska; Mirjana Popovska; Violeta Anastasovska ; Mirjana Kocova ; Lidita Zendeli-Bedzeti; Cena Dimova; Angela Taseva | 25-Sep-2018 | Article | |
Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH) | Kocova, M ; Siegel, S F; Wenger, S L; Lee, P A; Nalesnik, M; Trucco, M | 13-Feb-1995 | Article | |
Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA | Kocova, M ; Siegel, S F; Wenger, S L; Lee, P A; Trucco, M | 17-Jul-1993 | Article | |
Detection of Y-Chromosome Sequences in Gonadal Tissue of Patients with Turner's Syndrome (45,X) | Kocova, Mirjana ; Siegel, Selma F.; Nalesnick, Michael; Trucco, Massimo | 8-Sep-1994 | Article | |
Diagnostic approach in children with unusual symptoms of acquired hypothyroidism. When to look for pituitary hyperplasia? | Mirjana Kocova ; Nikolina Zdraveska ; Rozana Kacarska ; Elena Kochova | Mar-2016 | Article | |
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 | |
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 | |
Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase Deficiency | Anastasovska Violeta ; Milenković Tatjana ; Kocova Mirjana | Jan-2015 | Article | |
Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies | Pörksen, Sven; Laborie, Lene Bjerke; Nielsen, Lotte; Louise Max Andersen, Marie; Sandal, Tone; de Wet, Heidi; Schwarcz, Erik; Aman, Jan; Swift, Peter; Kocova, Mirjana ; Schönle, Eugen J; de Beaufort, Carine; Hougaard, Philip; Ashcroft, Frances; Molven, Anders; Knip, Mikael; Mortensen, Henrik B; Hansen, Lars; Njølstad, Pål R | 23-Sep-2010 | Article |