Browsing by Author Kochova, Mirjana
Showing results 82 to 101 of 140
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| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| 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 | |
| Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of Macedonia | Anastasovska Violeta ; Kocova Mirjana | Oct-2016 | Article | |
| Non-radioisotopic typing of human leukocyte antigen class II genes on microplates | Giorda, R; Lampasona, V; Kocova, M ; Trucco, M | Nov-1993 | Article | |
| A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia | Violeta Anastasovska ; Mirjana Kocova ; Nikolina Zdraveska ; Maja Stojiljkovic; Anita Skakic; Kristel Klaassen; Sonja Pavlovic | 14-Mar-2021 | Article | |
| Novel Genotype in Two Siblings with 5-α-reductase 2 Deficiency: Different Clinical Course due to the Time of Diagnosis | M Kocova ; D Plaseska-Karanfilska; P Noveski; M Kuzmanovska | Dec-2019 | Article | |
| Novel glucokinase gene mutation in the first Macedonian family tested for MODY | M. Kocova ; L. Elblova; S. Pruhova; J. Lebl; P. Dusatkova | Aug-2017 | Article | |
| Old syndrome-new approach: Mauriac syndrome treated with continuous insulin delivery | Mirjana Kocova ; Liljana Milenkova | 2018 | Article | |
| 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 | |
| Organochloride Pesticides in Macedonian Girls With Premature Sexual Development | M Krstevska-Konstantinova ; M Kocova ; C Charlier; J Bourguignon | 1-Apr-2007 | Article | |
| Osteopetrosis in infancy | M Delidzakova; T Nikolova; N Grivceva; A Gordova; R Dzarlieva; M Kocova | 1977 | Article | |
| A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia | Anastasovska, V ; Kocova, E; Kocova, M | 1-Jan-2010 | Article | |
| Parent and health professional perspectives in the management of adolescents with diabetes: development of assessment instruments for international studies | Hoey, Hilary; McGee, Hannah M; Fitzgerald, Michael; Mortensen, Henrik B; Hougaard, Philip; Lynggaard, Helle; Skovlund, Soren E; Aanstoot, Henk-Jan; Chiarelli, Francesco; Daneman, Denis; Danne, Thomas; Dorchy, Harry; Garandeau, Patrick; Greene, Stephen; Holl, Reinhard; Kaprio, Eero; Kocova, Mirjana ; Martul, Pedro; Matsuura, Nobuo; Robertson, Kenneth; Schoenle, Eugen; Sovik, Oddmund; Swift, Peter; Tsou, Rosa Maria; Vanelli, Maurizio; Aman, Jan | Aug-2006 | Article | |
| Persistent differences among centers over 3 years in glycemic control and hypoglycemia in a study of 3,805 children and adolescents with type 1 diabetes from the Hvidøre Study Group | Danne, T; Mortensen, H B; Hougaard, P; Lynggaard, H; Aanstoot, H J; Chiarelli, F; Daneman, D; Dorchy, H; Garandeau, P; Greene, S A; Hoey, H; Holl, R W; Kaprio, E A; Kocova, M ; Martul, P; Matsuura, N; Robertson, K J; Schoenle, E J; Søvik, O; Swift, P G; Tsou, R M; Vanelli, M; Aman, J | Aug-2001 | Article | |
| Phaeochromocytoma associated with reversible renal artery stenosis | Kuzmanovska, D; Sahpazova, E; Kocova, M ; Damjanovski, G; Popov, Z | Oct-2001 | Article | |
| Phenotypic variations in Wolf-Hirschhorn syndrome | E Sukarova-Angelovska ; M Kocova ; V Sabolich; S Palcevska; N Angelkova | Jun-2014 | Article | |
| Phenylketonuria screening in the Republic of Macedonia | Mirjana Kocova ; Violeta Anastasovska | 2016 | Article |