Resultados da pesquisa por Autor

1

Phenylketonuria screening in the Republic of Macedonia

Phenylketonuria screening in the Republic of Macedonia

Por Kocova, Mirjana, Anastasovska, Violeta
Publicado no Orphanet J Rare Dis (2016)

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2

Comments on ‘Newborn screening in southeastern Europe’ published in Molecular Genetics and Metabolism, 2014 Sept–Oct;113(1–2):42–45 by U. Groselj, M. ZerjavTansek, A. Smon, N. Angelkova, D. Anton, I. Baric, M. Djordjevic, L. Grimci, M. Ivanova, A. Kadam, V. Mulliqi Kotori, H. Maksic, O. Marginean, O. Margineanu, O. Milijanovic, F. Moldovanu, M. Muresan, S. Murko, M. Nanu, B. Repic Lampert, M. Samardzic, V. Sarnavka, A. Savov, M. Stojiljkovic, B. Suzic, R. Tincheva, H. Tahirovic, A. Toromanovic, N. Usurela, T. Battelino

Comments on ‘Newborn screening in southeastern Europe’ published in Molecular Genetics and Metabolism, 2014 Sept–Oct;113(1–2):42–45 by U. Groselj, M. ZerjavTansek, A. Smon, N. Ange...

Por Kocova, Mirjana, Anastasovska, Violeta
Publicado no Mol Genet Metab Rep (2015)

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3

Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of Macedonia

Newborn Screening for Thyroid-stimulating Hormone as an Indicator for Assessment of Iodine Status in the Republic of Macedonia

Por Anastasovska, Violeta, Kocova, Mirjana
Publicado no J Med Biochem (2016)

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4

Direct molecular diagnosis of CYP21A2 point mutations in Macedonian and Serbian patients with 21-hydroxylase deficiency

Direct molecular diagnosis of CYP21A2 point mutations in Macedonian and Serbian patients with 21-hydroxylase deficiency

Por Anastasovska Violeta, Milenković Tatjana, Kocova Mirjana
Publicado em 2015-01-01

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5

Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase Deficiency

Direct Molecular Diagnosis of CYP21A2 Point Mutations in Macedonian and Serbian Patients with 21-Hydroxylase Deficiency

Por Anastasovska, Violeta, Milenković, Tatjana, Kocova, Mirjana
Publicado no J Med Biochem (2015)

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6

Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-up

Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-up

Por Kocova, Mirjana, Janevska, Vesna, Anastasovska, Violeta
Publicado no Endocr Connect (2018)

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7

The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family

The impact of CYP21A2 (P30L/I172N) genotype on female fertility in one family

Por Kocova, Mirjana, Anastasovska, Violeta, Bitovska, Iskra
Publicado no Eur J Med Res (2019)

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8

Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood

Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood

Por Kocova, Mirjana, Zdraveska, Nikolina, Zdravkovska, Maja, Anastasovska, Violeta, Pop Gjorceva, Daniela
Publicado no SAGE Open Med Case Rep (2016)

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Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism

Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism

Por Zdraveska, Nikolina, Zdravkovska, Maja, Anastasovska, Violeta, Sukarova-Angelovska, Elena, Kocova, Mirjana
Publicado no Endocr Connect (2018)

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Detection of Virus Herpes Simplex Type 1 in Patients with Chronic Periodontal Disease

Detection of Virus Herpes Simplex Type 1 in Patients with Chronic Periodontal Disease

Por Ivanovska-Stojanoska, Marija, Popovska, Mirjana, Anastasovska, Violeta, Kocova, Mirjana, Zendeli-Bedzeti, Lidita, Dimova, Cena, Taseva, Angela
Publicado no Open Access Maced J Med Sci (2018)

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