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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false
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Results 1-12 of 12 (Search time: 0.006 seconds).
| Преглед | Наслов | Автор(ите) | Датум на издавање | Тип | |
|---|---|---|---|---|---|
| 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-фев-2018 | Proceeding article | |
| 2 | 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-апр-2019 | Proceeding article | |
| 3 | Evaluation of selective newborn screening for inborn errors of metabolism in Macedonia | Anastasovska, Violeta ; Kochova, Mirjana | 14-окт-2018 | Proceeding article | |
| 4 | Frequency of detected genotypes in patients with salt-wasting form of 21-hydroxylase deficiency | Kochova, Mirjana ; Anastasovska, Violeta | 17-апр-2019 | Proceeding article | |
| 5 | 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-окт-2018 | Proceeding article | |
| 6 | 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-апр-2019 | Proceeding article | |
| 7 | 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-окт-2018 | Proceeding article | |
| 8 | Myopathic form of carnitine palmitoyltransferase II deficiency – Case report | Angelkova, N.; Sukarova-Angelovska, E.; Kocova, M. ; Duma, F. ; Sabolic, V. | јун-2017 | Proceeding article | |
| 9 | Targeted sequencing of dyshormonogenesis-associated genes in Macedonian cases with congenital hypothyroidism and gland-in-situ reveals a low mutation frequency | Zdraveska, Nikolina ; Kocova, Mirjana ; Nicholas, Adeline K; Anastasovska, Violeta ; Schoenmakers, Nadia | 2-ное-2018 | Proceeding article | |
| 10 | Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated? | Sukarova Angelovska, E ; Kocova, M ; Zorcec, T | 2015 | Proceeding article | |
| 11 | Transient congenital hypothyroidism in preterm and full-term infants | Zdraveska, Nikolina ; Anastasovska, Violeta ; Kochova, Mirjana | 9-јун-2019 | Proceeding article | |
| 12 | Variations in incidence of congenital hypothyroidism in association with changes of cutoff value | Pesevska, Milica; Anastasovska, Violeta ; Taseva, Elizabeta; Zdraveska, Nikolina ; Gurzanova-Durnev, Liljana; Kochova, Mirjana | 3-окт-2018 | Proceeding article |