Kochova, Mirjana
Full Name
Kochova, Mirjana
Vernacular Name
Мирјана Кочова
Variants
Kocova Mirjana
Kocova M
M Kocova
Mirjana Kochova
Мирјана Кочова
Kocova M
M Kocova
Mirjana Kochova
Мирјана Кочова
Main Affiliation
Email
mirjana.kochova@medf.ukim.edu.mk
Other emails
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Date issued
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Results 1-20 of 25 (Search time: 0.015 seconds).
| Preview | Title | Author(s) | Issue Date | Type | |
|---|---|---|---|---|---|
| 1 | 46, XX DSD with diphallus as a part of a multimalformative syndrome - a case report | Shukarova Angelovska, Elena ; Kochova, Mirjana ; Ilieva, Gordana; Anastasovska, Violeta ; Krstevska Konstantinova, Marina ; Filev, G | 23-Feb-2018 | Proceeding article | |
| 2 | ACUTE MYELOBLASTIC LEUKEMIA IN CHILDREN, TREATMENT AND PROGNOSIS 125 | Muratovska, O ; Zisovski, N; Glamocanin, S; Martinova, K ; Kocova, M ; Pashu, M; Antevska, Z | May-1997 | Proceeding article | |
| 3 | 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 | |
| 4 | 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 | |
| 5 | Evaluation of selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kochova, Mirjana | 14-Oct-2018 | Proceeding article | |
| 6 | Frequency of detected genotypes in patients with salt-wasting form of 21-hydroxylase deficiency | Kochova, Mirjana ; Anastasovska, Violeta | 17-Apr-2019 | Proceeding article | |
| 7 |  | Genetics of transient congenital hypothyroidism | Zdraveska, Nikolina ; Anastasovska, Violeta ; Kocova Mirjana | 11-Jun-2022 | Proceeding article |
| 8 | Incidence of congenital hypothyroidism in different regions of Macedonia - sixteen years newborn thyroid screening | Anastasovska, Violeta ; Pesevska, Milica; Taseva, Elizabeta; Sukarova-Angelovska, Elena; Zdraveska, Nikolina ; Gurzanova-Durnev Ljiljana; Kochova, Mirjana | 3-Oct-2018 | Proceeding article | |
| 9 | Incidence of Congenital Hypothyroidism in the Republic of North Macedonia in Correlation with TSH Cutoff Level | Anastasovska, Violeta ; Pesevska, Milica; Kocova, Mirjana ; Shukarova Angelovska, Elena ; Fakovic, Nermina; Karishik, Senada | 10-Nov-2021 | Proceeding article | |
| 10 | 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 | |
| 11 | 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 | |
| 12 | 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 | |
| 13 | 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 | |
| 14 | 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 | |
| 15 | Myopathic form of carnitine palmitoyltransferase II deficiency – Case report | Angelkova, N.; Sukarova-Angelovska, E.; Kocova, M. ; Duma, F. ; Sabolic, V. | Jun-2017 | Proceeding article | |
| 16 | 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 | |
| 17 | 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 | |
| 18 | Remission phase of type 1 diabetes in children in the Republic of Macedonia | Kocova, Mirjana J ; Sukarova-Angelova, Elena P ; Krstevska-Konstantinova, Marina M | Sep-2000 | Proceeding article | |
| 19 |  | Report of a rare case of acute megakaryocytic leukemia | Svetlana Stankovic ; Gordana Petrusevska ; Mirjana Kocova ; Sonja Genadieva Stavric ; Marija Lozance; Aleksandra Pivkova ; Arif Latifi; Lidija Cevreska | 2005 | Proceeding article |
| 20 | Seven years experience with selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kocova Mirjana ; Shukarova Angelovska, Elena ; Pesevska, Milica; Zdraveska, Nikolina | 10-Nov-2021 | Proceeding article |