Zobrazeno 1 - 10
of 75
pro vyhledávání: '"V., Anastasovska"'
Autor:
S., Fustik1 tojkaf@yahoo.com, V., Anastasovska2, D., Plaseska-Karanfilska3, A., Stamatova1, L., Spirevska1, M., Pesevska2, M., Terzikj3, M., Vujovic3
Publikováno v:
Balkan Journal of Medical Genetics. 2021, Vol. 24 Issue 1, p41-45. 5p.
Autor:
S. Fustik, V. Anastasovska, D. Plaseska Karanfilska, A. Stamatova, L. Spirevska, M. Pesevska, M. Terzikj, M. Vujovic
Publikováno v:
Journal of Cystic Fibrosis. 21:S63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21729bbdab18128b4ed305257c301b82
https://doi.org/10.1016/s1569-1993(22)00345-9
https://doi.org/10.1016/s1569-1993(22)00345-9
Publikováno v:
Journal of Cystic Fibrosis. 20:S43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3578f02ade87f6397e9d4b84c2f3481
https://doi.org/10.1016/s1569-1993(21)01044-4
https://doi.org/10.1016/s1569-1993(21)01044-4
Autor:
M. Pesevska, M. Terzikj, N. Fakovic, Ana Stamatova, V. Anastasovska, D. Plaseska Karanfilska, S. Fustik, L. Spirevska
Publikováno v:
Journal of Cystic Fibrosis. 20:S42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f6ec38ac2b968345ddd1d5e2350e6b6
https://doi.org/10.1016/s1569-1993(21)01039-0
https://doi.org/10.1016/s1569-1993(21)01039-0
Autor:
M. Pesevska, M. Terzikj, D. Plaseska Karanfilska, L. Spirevska, S. Fustikj, Ana Stamatova, V. Anastasovska
Publikováno v:
Journal of Cystic Fibrosis. 19:S59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14916dce8327a615277e14f33501da32
https://doi.org/10.1016/s1569-1993(20)30353-2
https://doi.org/10.1016/s1569-1993(20)30353-2
Publikováno v:
Balkan Journal of Medical Genetics
Balkan Journal of Medical Genetics, Vol 17, Iss 1, Pp 31-35 (2014)
Balkan Journal of Medical Genetics, Vol 17, Iss 1, Pp 31-35 (2014)
Congenital hypothyroidism (CH) is the most common preventable cause of mental retardation in children. Diagnosis is difficult at birth without neonatal screening. Neonatal thyroid screening was established in Prilep, Republic of Macedonia as an integ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5788bc255427f6403073983b9526d48a
https://doi.org/10.2478/bjmg-2014-0024
https://doi.org/10.2478/bjmg-2014-0024
Akademický článek
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Publikováno v:
Contributions of Macedonian Academy of Sciences & Arts. 2008, Vol. 29 Issue 1, p93-106. 14p. 5 Charts.
Publikováno v:
Balkan Journal of Medical Genetics, Vol 13, Iss 1, Pp 17-21 (2010)
A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal HyperplasiaNonclassical congenital adrenal hyperplasia (NCAH) is an autosomal recessive imbalance in cortisol synthesis with adrenal androgen excess. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2316fffd4b1fba7b5203943f9a9b763e
https://doaj.org/article/cc7b67ddcaff480a894ddcb09803e939
https://doaj.org/article/cc7b67ddcaff480a894ddcb09803e939
Autor:
V Anastasovska, M Kocova
Publikováno v:
Balkan Journal of Medical Genetics, Vol 13, Iss 2, Pp 27-33 (2010)
Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of MacedoniaCongenital adrenal hyperplasia (CAH) is an autosomal recessive disorder. In 90-95% of cases it results from mutations in the gene for 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e757ca59bee223094243ef920f6eed91
https://doi.org/10.2478/v10034-010-0023-7
https://doi.org/10.2478/v10034-010-0023-7