Violeta Anastasovska - Search Results

Year	Number of Results
2005	1
2006	1
2010	2
2014	2
2015	3
2016	4
2017	2
2018	3
2019	2
2020	2
2021	2
2022	2
2023	2
2024	0

1

European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance.

Munck A, Berger DO, Southern KW, Carducci C, de Winter-de Groot KM, Gartner S, Kashirskaya N, Linnane B, Proesmans M, Sands D, Sommerburg O, Castellani C, Barben J; European CF Society Neonatal Screening Working Group (ECFS NSWG). Munck A, et al. J Cyst Fibros. 2023 May;22(3):484-495. doi: 10.1016/j.jcf.2022.09.012. Epub 2022 Nov 10. J Cyst Fibros. 2023. PMID: 36372700

2

Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Kocova M, Anastasovska V, Falhammar H. Kocova M, et al. Among authors: anastasovska v. Endocrine. 2020 Aug;69(2):262-277. doi: 10.1007/s12020-020-02323-3. Epub 2020 May 5. Endocrine. 2020. PMID: 32367336 Free PMC article. Review.

3

Global impact of COVID-19 on newborn screening programmes.

Koracin V, Loeber JG, Mlinaric M, Battelino T, Bonham JR, Groselj U; COVID-NBS ISNS global network. Koracin V, et al. BMJ Glob Health. 2022 Mar;7(3):e007780. doi: 10.1136/bmjgh-2021-007780. BMJ Glob Health. 2022. PMID: 35236661 Free PMC article.

4

Phenylketonuria screening in the Republic of Macedonia.

Kocova M, Anastasovska V. Kocova M, et al. Among authors: anastasovska v. Orphanet J Rare Dis. 2016 Aug 5;11(1):112. doi: 10.1186/s13023-016-0483-2. Orphanet J Rare Dis. 2016. PMID: 27496147 Free PMC article.

5

Genetics of Gland-in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia.

Zdraveska N, Kocova M, Nicholas AK, Anastasovska V, Schoenmakers N. Zdraveska N, et al. Among authors: anastasovska v. Front Endocrinol (Lausanne). 2020 Jul 14;11:413. doi: 10.3389/fendo.2020.00413. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32765423 Free PMC article.

6

First insights into the genetics of 21-hydroxylase deficiency in the Roma population.

Kocova M, Anastasovska V, Petlichkovski A, Falhammar H. Kocova M, et al. Among authors: anastasovska v. Clin Endocrinol (Oxf). 2021 Jul;95(1):41-46. doi: 10.1111/cen.14447. Epub 2021 Mar 2. Clin Endocrinol (Oxf). 2021. PMID: 33605469

7

Regional Variation in the Incidence of Congenital Hypothyroidism in Macedonia.

Anastasovska V, Sukarova-Angelovska E, Pesevska M, Taseva E, Kocova M. Anastasovska V, et al. Int J Neonatal Screen. 2017 Aug 21;3(3):22. doi: 10.3390/ijns3030022. Int J Neonatal Screen. 2017. PMID: 33535365 Free article.

8

Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia.

Anastasovska V, Kocova M. Anastasovska V, et al. J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):405-409. doi: 10.1515/jpem-2016-0178. J Pediatr Endocrinol Metab. 2017. PMID: 27658135

9

Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years.

Anastasovska V, Pesevska M, Zdraveska N, Zafirova B, Jovcevska JM, Kocova M. Anastasovska V, et al. Turk J Pediatr. 2023;65(2):227-234. doi: 10.24953/turkjped.2022.594. Turk J Pediatr. 2023. PMID: 37114688 Free article.

10

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

Kocova M, Anastasovska V, Bitovska I. Kocova M, et al. Among authors: anastasovska v. Eur J Med Res. 2019 Jun 19;24(1):21. doi: 10.1186/s40001-019-0379-4. Eur J Med Res. 2019. PMID: 31217034 Free PMC article.

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