V. Anastasovska

发表

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

M. Kocova, V. Janevska, V. Anastasovska, 2018, Endocrine connections.

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

M. Kocova, H. Falhammar, V. Anastasovska, 2020, Endocrine.

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

M. Kocova, M. Krstevska-Konstantinova, V. Anastasovska, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy

M. Kocova, V. Anastasovska, 2007 .

Genotype-Phenotype Correlation in CAH Patients with Severe CYP21A2 Point Mutations in the Republic of Macedonia

M. Kocova, V. Anastasovska, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood

M. Kocova, M. Zdravkovska, Nikolina Zdraveska, 2016 .

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

M. Kocova, M. Stojiljkovic, S. Pavlovic, 2021, Endocrine.

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

M. Kocova, H. Falhammar, A. Petlichkovski, 2021, Clinical endocrinology.

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

M. Kocova, I. Bitovska, V. Anastasovska, 2019, European Journal of Medical Research.

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

M. Kocova, T. Milenković, V. Anastasovska, 2014, Journal of medical biochemistry.

A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia

M. Kocova, V. Anastasovska, E. Kočová, 2010 .

Detected heterozygotes during the molecular analysis of the common CYP21A2 point mutations in Macedonian patients with congenital adrenal hyperplasia and their relatives.

M. Kocova, V. Anastasovska, 2010, Prilozi.

Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia

M. Kocova, V. Anastasovska, 2010 .

Ethnicity and incidence of congenital hypothyroidism in the capital of Macedonia

M. Kocova, V. Anastasovska, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Methodological and organizational aspects of newborn screening for congenital hypothyroidism in Macedonia.

M. Kocova, V. Anastasovska, B. Gjurkova, 2008, Prilozi.

Regional Variation in the Incidence of Congenital Hypothyroidism in Macedonia.

M. Kocova, E. Sukarova-Angelovska, V. Anastasovska, 2017, International journal of neonatal screening.

Impact of Lower Screening TSH Cutoff Level on the Increasing Prevalence of Congenital Hypothyroidism

M. Kocova, V. Anastasovska, 2017 .

Impact of Lower Screening TSH Cutoff Level on the Increasing Incidence of Congenital Hypothyroidism

M. Kocova, V. Anastasovska, 2017 .

High Incidence of Congenital Hypothyroidism in One Region of the Republic of Macedonia

M. Kocova, V. Anastasovska, R. Koviloska, 2014, Balkan journal of medical genetics : BJMG.

Phenylketonuria screening in the Republic of Macedonia

M. Kocova, V. Anastasovska, 2016, Orphanet Journal of Rare Diseases.

Phenylketonuria screening in the Republic

M. Kocova, V. Anastasovska, 2016 .

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

M. Kocova, E. Sukarova-Angelovska, M. Zdravkovska, 2018, Endocrine connections.

Erythrocyte glucose-6-phosphate dehydrogenase activity in laboratory rats treated with amoxiclav, lidaprim and 1-chloro-2,4-dinitrobenzen.

V. Stojkovski, V. Anastasovska, Bozidarka Dosić-Markovska, 2005, Prilozi.

MOLECULAR DETECTION OF VIRUS HERPES SIMPLEX TYPE 1(HSV-1) , VIRUS HERPES SIMPLEX TYPE 2(HSV-2), CYTOMEGALOVIRUS(HCMV) and EPSTEIN-BARRVIRUS (EBV) IN SUPRA-GI

M. Popovska, V. Anastasovska, S. Todorovska, 2018, Knowledge International Journal.

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

M. Kocova, M. Popovska, C. Dimova, 2018, Open access Macedonian journal of medical sciences.

Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism

M. Kocova, Nikolina Zdraveska, V. Anastasovska, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Clinical Practice: Experience with newborn screening for congenital hypothyroidism in the Republic of Macedonia—a multiethnic country

M. Kocova, E. Sukarova-Angelovska, V. Anastasovska, 2015, European Journal of Pediatrics.

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

M. Kocova, A. Nicholas, N. Schoenmakers, 2020, Frontiers in Endocrinology.

Effects of different dietary fatty acid supplements upon lipoprotein metabolism and lipid peroxides production in hyperlipidemic rats.

V. Anastasovska, Bozidarka Dosić-Markovska, Jasmina Dimitrova-Sumkovska, 2006, Prilozi.

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

V. Anastasovska, S. Fuštik, M. Vujović, 2021, Balkan journal of medical genetics : BJMG.

Regional Variation in the Incidence of Congenital Hypothyroidism in Macedonia.

M. Kocova, E. Sukarova-Angelovska, V. Anastasovska, 2017, International Journal of Neonatal Screening.

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

M. Kocova, B. Zafirova, Nikolina Zdraveska, 2023, The Turkish journal of pediatrics.

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

M. Kocova, V. Anastasovska, 2016, Journal of medical biochemistry.