Browsing by Author Kochova, Mirjana
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| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| Major karyotypic abnormalities in a near-tetraploid erythroleukemia | Kocova, M J ; Sandberg, A A | Jun-1985 | Article | |
| The many faces of oral-facial-digital syndrome | E Sukarova-Angelovska ; N Angelkova; S Palcevska-Kocevska; M Kocova | Jun-2012 | Article | |
| Meal-stimulated glucagon release is associated with postprandial blood glucose level and does not interfere with glycemic control in children and adolescents with new-onset type 1 diabetes | Pörksen, Sven; Nielsen, Lotte B; Kaas, Anne; Kocova, Mirjana ; Chiarelli, Francesco; Orskov, Cathrine; Holst, Jens J; Ploug, Kenneth B; Hougaard, Philip; Hansen, Lars; Mortensen, Henrik B | Aug-2007 | Article | |
| Metabolic outcomes in young children with type 1 diabetes differ between treatment centers: the Hvidoere Study in Young Children 2009 | de Beaufort, Carine E; Lange, Karin; Swift, Peter G F; Aman, Jan; Cameron, Fergus; Castano, Luis; Dorchy, Harry; Fisher, Lynda K; Hoey, Hilary; Kaprio, Eero; Kocova, Mirjana ; Neu, Andreas; Njolstad, Pal R; Phillip, Moshe; Schoenle, Eugen; Robert, Jean J; Urukami, Tatsuhiko; Vanelli, Maurizio; Danne, Thomas; Barrett, Tim; Chiarelli, Franco; Aanstoot, Henk J; Mortensen, Henrik B | Sep-2013 | 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 | |
| Micro-chimerism is associated with a lower incidence of chronic rejection after lung transplantation | Banas, R.; Keenan, R.; Sommers, E.; Spichty, K.; Yousem, S.; Kocova, M. ; Trucco, M.; Starzi, T.; Griffith, B.; Zeevi, A. | Jan-1994 | Proceeding article | |
| Microchimerism linked to cytotoxic T lymphocyte functional unresponsiveness (clonal anergy) in a tolerant renal transplant recipient | Burlingham, W J; Grailer, A P; Fechner, J H; Kusaka, S; Trucco, M; Kocova, M ; Belzer, F O; Sollinger, H W | 27-Apr-1995 | Article | |
| Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy | Anastasovska, V ; Kocova, M | 1-Jan-2007 | Article | |
| Molecular detection of Herpes simplex virus type 1, Herpes simplex virus type 2, Cytomegalovirus and Epstein-barr virus in subgingival dental plaque in patients with periodontal disease | Ivanovska-Stojanovska, Marija; Popovska, Mirjana ; Anastasovska, Violeta ; Kochova, Mirjana ; Zendeli Bedjeti, Lindita; Atanasovska-Stojanovska, Aneta; Todorovska, Sashka | 17-Apr-2019 | Proceeding article | |
| Molecular diagnosis of MCAD in the Macedonian neonates with elevated medium-chain acylcarnitines identified through MS/MS-based newborn screening | Anastasovska, Violeta ; Kocova, Mirjana ; Zdraveska, Nikolina ; Tesovnik, Tine; Debeljak, Maruša; Kovač, Jernej | 2022 | Proceeding article | |
| Molecular IDDM epidemiology: international studies. WHO DiaMond Molecular Epidemiology Sub-Project Group | Dorman, J S; McCarthy, B; McCanlies, E; Kramer, M K; Vergona, R J; Stone, R; Steenkiste, A R; Kocova, M ; Trucco, M | Oct-1996 | Proceeding article | |
| Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiency | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article | |
| Multiple molecular mechanisms of insulin receptor dysfunction in a patient with Donohue syndrome | Whitehead, J P; Soos, M A; Jackson, R; Tasic, V ; Kocova, M ; O'Rahilly, S | Aug-1998 | Article | |
| Myopathic form of carnitine palmitoyltransferase II deficiency – Case report | Angelkova, N.; Sukarova-Angelovska, E.; Kocova, M. ; Duma, F. ; Sabolic, V. | Jun-2017 | Proceeding article | |
| Naturally occurring amino acid substitutions at Arg1174 in the human insulin receptor result in differential effects on receptor biosynthesis and hybrid formation, leading to discordant clinical phenotypes | Rau, H; Kocova, M ; O'Rahilly, S; Whitehead, J P | Jul-2000 | 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 | |
| A new familial mutation (R133G) in the SRY gene | D Plaseska-Karanfilska; P Noveski; K Kuzevska; N Basheska ; M Kocova ; GD Efremov | May-2007 | Article | |
| A new familial mutation in the SRY gene (Arg133Gly) | Plaseska-Karanfilska, Dijana; Noveski, Predrag; Kuzevska, Klementina; Basheska, Neli ; Kochova, Mirjana ; Efremov, Gjorgji | Sep-2006 | 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 |