Robert Petrovic

Bratislava, BL, Slovakia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Prevalence of clinical manifestations among patients with hypophosphatasia in Central and Eastern European countries.

Prevalence of clinical manifestations among patients with hypophosphatasia in Central and Eastern European countries.

Journal: Frontiers in endocrinology

Published: May 27, 2026

SOD1 Variants in Patients With Amyotrophic Lateral Sclerosis in Central Eastern Europe: From Genetic Testing to SOD1 Targeted Therapy.

SOD1 Variants in Patients With Amyotrophic Lateral Sclerosis in Central Eastern Europe: From Genetic Testing to SOD1 Targeted Therapy.

Journal: European journal of neurology

Published: April 01, 2026

Derivation of a new induced pluripotent stem cell line ORIONi004-A for modelling Duchenne muscular dystrophy.

Derivation of a new induced pluripotent stem cell line ORIONi004-A for modelling Duchenne muscular dystrophy.

Journal: Stem cell research

Published: February 16, 2026

Late-onset epi-cblC methylmalonic aciduria with tissue-variable MMACHC promoter methylation due to a stop retained PRDX1 variant.

Late-onset epi-cblC methylmalonic aciduria with tissue-variable MMACHC promoter methylation due to a stop retained PRDX1 variant.

Journal: Clinical epigenetics

Published: August 15, 2025

Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients.

Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients.

Journal: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia

Published: January 21, 2024

Short tandem repeats genotyping of gestational choriocarcinoma - our experiences.

Short tandem repeats genotyping of gestational choriocarcinoma - our experiences.

Journal: Taiwanese journal of obstetrics & gynecology

Published: October 19, 2023

Congenital Proximal Radioulnar Synostosis in an Elite Athlete-Case Report.

Congenital Proximal Radioulnar Synostosis in an Elite Athlete-Case Report.

Journal: Medicina (Kaunas, Lithuania)

Published: January 23, 2023

Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Journal: Frontiers in endocrinology

Published: December 29, 2022

Fabry Disease in Slovakia: How the Situation Has Changed over 20 Years of Treatment.

Fabry Disease in Slovakia: How the Situation Has Changed over 20 Years of Treatment.

Journal: Journal of personalized medicine

Published: April 21, 2022

Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL - experience from Slovakia.

Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL - experience from Slovakia.

Journal: Neurogenetics

Published: March 14, 2022

Partial hydatidiform moles with unclear histopathological profile - importance of genetic diagnostics.

Partial hydatidiform moles with unclear histopathological profile - importance of genetic diagnostics.

Journal: Ceska gynekologie

Published: January 18, 2022

TREM2 coding variants in Slovak Alzheimer's disease patients.

TREM2 coding variants in Slovak Alzheimer's disease patients.

Journal: Journal of integrative neuroscience

Published: December 13, 2021

Showing 1-12 of 23

Last Updated: 09/26/2026