Concepedia

Author

Róbert Petrovič

Comenius University BratislavaORCID

Also Known As

Jana Behunova, R Petrovic, R Petrović, R. Petrovic, R. Petrović, R. Petrović, R. Petrovič, R.J. Petrović, Rastko Petrović, Robert Petrovic

67

Publications

224

Citations

9

H-Index

31

Concepts

All Affiliations

Comenius University BratislavaUniversity Hospital Bratislava
RP

About

Róbert Petrovič is an author at Comenius University Bratislava specializing in medicine, genetics, and neurology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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Public Health

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3

Social Sciences

1

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16

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Cell Biology

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10

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Molecular Genetics

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Róbert Petrovič

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8

Publications

129

Citations

8

H-Index

YearCitations

Rapid and simple method for determination of N<sup>ε</sup>‐(carboxymethyl)lysine and N<sup>ε</sup>‐(carboxyethyl)lysine in urine using gas chromatography[sol ]mass spectrometry

Róbert Petrovič, Ján Futas, Ján Chandoga,

Biomedical Chromatography

2005

29

Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern

Katharina Schoner, Martina Witsch‐Baumgartner, Jana Behunova,

Birth Defects Research

2019

21

Adult onset cerebral form of X-linked adrenoleukodystrophy with dementia of frontal lobe type with new L160P mutation in ABCD1 gene

Stanislav Šutovský, Róbert Petrovič, Ján Chandoga,

Journal of the Neurological Sciences

2007

17

Study of possibility in raising maize inbred lines with two embryos

N. Pešev, Róbert Petrovič, Lj. Zečević,

Theoretical and Applied Genetics

1976

16

Neuropathology and biochemistry of early onset familial Alzheimer’s disease caused by presenilin-1 missense mutation Thr116Asn

Stanislav Šutovský, Tomáš Smolek, Peter Turčáni,

Journal of Neural Transmission

2018

16

Frequencies of polymorphisms in CYP2C9 and VKORC1 genes influencing warfarin metabolism in Slovak population: implication for clinical practice

Ľubica Krajčíová, Ľudmila Déžiová, Róbert Petrovič,

Bratislavské lekárske listy/Bratislava medical journal

2014

10

Prevalence of Low Serum Alkaline Phosphatase and Hypophosphatasia in Adult Patients with Atypical Femur Fractures

Eleni Tsiantouli, Emmanuel Biver, Thierry Chevalley,

Calcified Tissue International

2022

10

A novel mutation in the PEX12 gene causing a peroxisomal biogenesis disorder

Jana Konkoľová, Róbert Petrovič, Ján Chandoga,

Molecular Biology Reports

2015

10

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