Zoran S. Gucev

St. Cyril And Methodius University In Skopje
Skopje, The former Yugoslav Republic of Macedonia

Last Updated: 09/26/2026

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Found 104 publications

Neurodevelopment of Critical ILL Neonates at the Age of 12 Months.

Neurodevelopment of Critical ILL Neonates at the Age of 12 Months.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)
Published: December 12, 2024

Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

Journal: European journal of human genetics : EJHG
Published: March 08, 2024

Compound Heterozygosity in Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4.

Compound Heterozygosity in Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)
Published: December 18, 2023

Two Brothers from Macedonia with Gitelman Syndrome.

Two Brothers from Macedonia with Gitelman Syndrome.

Journal: Balkan journal of medical genetics : BJMG
Published: August 14, 2023

Peripheral Insulin Edema and Pericardial Effusion in a 12-Year-Old Newly Diagnosed Girl with Type 1 Diabetes.

Peripheral Insulin Edema and Pericardial Effusion in a 12-Year-Old Newly Diagnosed Girl with Type 1 Diabetes.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)
Published: July 15, 2023

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

Journal: Journal of the American Society of Nephrology : JASN
Published: September 24, 2022

Alström Syndrome with Early Vision and Hearing Impairement.

Alström Syndrome with Early Vision and Hearing Impairement.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)
Published: July 17, 2022

Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2.

Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes-Brocks syndrome 2.

Journal: Human genetics
Published: July 08, 2022

Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries.

Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries.

Journal: Orphanet journal of rare diseases
Published: January 21, 2022

The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers.

The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers.

Journal: Orphanet journal of rare diseases
Published: November 15, 2021

In Memoriam Academic Momir Polenakovic, Pediatric Nephrology, Rare Diseases and Publishing in Macedonia.

In Memoriam Academic Momir Polenakovic, Pediatric Nephrology, Rare Diseases and Publishing in Macedonia.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)
Published: October 26, 2021

Posterior Urethral Valve and Prenataly Resolved Multicystic Dysplastic Kidney.

Posterior Urethral Valve and Prenataly Resolved Multicystic Dysplastic Kidney.

Journal: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)
Published: April 24, 2021
Showing 1-12 of 104

Last Updated: 09/26/2026