Velibor B. Tasic
Mother Theresa 17 St
Skopje, 1000, The former Yugoslav Republic of Macedonia
Skopje, 1000, The former Yugoslav Republic of Macedonia
Last Updated: 09/26/2026
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Found 157 publications
Beyond Living Donor Kidney Transplantation in COL4 Nephropathy - A Real-World Clinical Dilemma in Light of Current Guidelines.
Journal: Balkan journal of medical genetics : BJMG
Published: May 18, 2026
Beyond complement: comprehensive assessment of factor XIII plasma dynamics and genetics in atypical hemolytic uremic syndrome.
Journal: Research and practice in thrombosis and haemostasis
Published: April 18, 2026
Biallelic pathogenic variants in EXOSC3 mediate renal thrombotic microangiopathy of the kidney.
Journal: Kidney international
Published: February 10, 2026
Nephrotic Syndrome Induced by Tiopronin in a Male Patient with Cystinuria.
Journal: Balkan journal of medical genetics : BJMG
Published: November 07, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.
Journal: Nature communications
Published: October 09, 2025
Intermittent dark urine in a school-aged boy: a case of alkaptonuria.
Journal: Kidney international
Published: June 30, 2025
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency.
Journal: European journal of pediatrics
Published: June 17, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.
Journal: Nature communications
Published: November 16, 2024
COL4A5-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype.
Journal: Kidney international reports
Published: October 01, 2024
Survey of legislative frameworks and national recommendations governing paediatric maintenance haemodialysis in Europe.
Journal: Pediatric nephrology (Berlin, Germany)
Published: August 13, 2024
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Journal: American journal of human genetics
Published: July 22, 2024
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 08, 2024
Last Updated: 09/26/2026