Violeta Anastasovska

Skopje, 1000, The former Yugoslav Republic of Macedonia

Last Updated: 09/26/2026

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Found 23 publications

Current Status of Newborn Screening in Southeastern and Central Europe.

Current Status of Newborn Screening in Southeastern and Central Europe.

Journal: International journal of neonatal screening

Published: December 30, 2025

Medium-chain acyl-CoA dehydrogenase deficiency in North Macedonia - ten years experience.

Medium-chain acyl-CoA dehydrogenase deficiency in North Macedonia - ten years experience.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 08, 2024

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

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

Journal: The Turkish journal of pediatrics

Published: April 28, 2023

Two Years of Newborn Screening for Cystic Fibrosis in North Macedonia: First Experience.

Two Years of Newborn Screening for Cystic Fibrosis in North Macedonia: First Experience.

Journal: Balkan journal of medical genetics : BJMG

Published: August 27, 2021

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

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

Journal: Clinical endocrinology

Published: November 28, 2020

A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia.

A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia.

Journal: Endocrine

Published: October 06, 2020

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

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

Journal: Frontiers in endocrinology

Published: March 08, 2020

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

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

Journal: Endocrine

Published: February 12, 2020

Therapeutic challenges in a patient with the simple virilizing (SV) form of congenital adrenal hyperplasia (CAH) due to the P30L/I172N genotype.

Therapeutic challenges in a patient with the simple virilizing (SV) form of congenital adrenal hyperplasia (CAH) due to the P30L/I172N genotype.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 30, 2018

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.

Journal: Open access Macedonian journal of medical sciences

Published: July 07, 2018

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.

Journal: Endocrine connections

Published: March 05, 2018

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.

Journal: Endocrine connections

Published: January 10, 2018

Showing 1-12 of 23

Last Updated: 09/26/2026