Browsing by Author Kochova, Mirjana
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| Preview | Title | Author(s) | Issue Date | Type |
|---|---|---|---|---|
| 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 | |
| Efficacy and safety of a fixed combination of insulin degludec/insulin aspart in children and adolescents with type 1 diabetes: A randomized trial | Battelino, Tadej; Deeb, Larry C; Ekelund, Magnus; Kinduryte, Ona; Klingensmith, Georgeanna J; Kocova, Mirjana ; Kovarenko, Margarita; Shehadeh, Naim | 2018 | Article | |
| Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia | Violeta Anastasovska ; Mirjana Kocova | 1-Apr-2017 | Article | |
| Evaluation of a type 1 diabetes serum cohort by SELDI-TOF MS protein profiling | Albrethsen, Jakob; Kaas, Anne; Schönle, Eugen; Swift, Peter; Kocova, Mirjana ; Gammeltoft, Steen; Hansen, Lars; Mortensen, Henrik Bindesbøl | Mar-2009 | Article | |
| Evaluation of selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article | |
| Fine quantitation by competitive PCR of circulating donor cells in posttransplant chimeric recipients | Rudert, W A; Kocova, M ; Rao, A S; Trucco, M | 27-Oct-1994 | Article | |
| First insights into the genetics of 21-hydroxylase deficiency in the Roma population | Mirjana Kocova ; Violeta Anastasovska ; Aleksandar Petlichkovski ; Henrik Falhammar | 19-Feb-2021 | Article | |
| Frequency of detected genotypes in patients with salt-wasting form of 21-hydroxylase deficiency | Kochova, Mirjana ; Anastasovska, Violeta | 17-Apr-2019 | Proceeding article | |
| Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism | Nikolina Zdraveska ; Violeta Anastasovska ; Mirjana Kocova | 1-Jul-2016 | Article | |
| Genetic analysis of HLA DRB1, DQA1 and DQB1 alleles and susceptibility to IDDM in Chilean subjects. Chile IDDM Study Group | Perez-Bravo, F; Serrano-Rios, M; Gutierrez-Lopez, M D; Calvillan, M; Garcia de los Rios, M; Kocova, M ; Dorman, J; Trucco, M | Mar-1995 | Article |