György Benedek
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
György Benedek has a total of 43 co-authors. Here are the top co-authors by number of shared publications:
- Gyongyi Horvath
Department of Physiology, Albert Szent-Györgyi Medical School, University of Szeged, Dóm tér 10, H-6720 Szeged, Hungary; Department of Medical Physics and Informatics, Albert Szent-Györgyi Medical School, University of Szeged, Korányi fasor 9, H-6720 Szeged, Hungary; Sztárai Institute, University of Tokaj, Eötvös út 7, H-3950 Sárospatak, Hungary
9 shared publications - Gabriella Kekesi
Department of Physiology, Albert Szent-Györgyi Medical School, University of Szeged, Dóm tér 10, H-6720 Szeged, Hungary
8 shared publications - Alexandra Büki
Department of Physiology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary
4 shared publications - Zita Petrovszki
Institute of Physical Education and Sport Medicine, Juhász Gyula Faculty of Education, University of Szeged, Hattyas sor 10., H-6725 Szeged, Hungary
4 shared publications - Gábor Braunitzer
DicomLAB Dental, Ltd., 6726 Szeged, Hungary
3 shared publications - Arpad Safrany-Fark
Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, University of Szeged, Tisza L. krt. 64, H-6720 Szeged, Hungary
2 shared publications
Latest Publications
- Open Access
Immunohistochemical Analysis of a Vitreous Membrane Removed from a Patient with Incontinentia Pigmenti-Related Retinal Detachment
This is a case history of a 23-year-old woman suffering from incontinentia pigmenti (IP). The patient’s vision in the left eye started to deteriorate due to cataract progression at the age of 22, and by the age of 23, it dropped from 0.9 to 0.04. Ultrasound examination confirmed tractional vitreoretinal membranes. Vitrectomy was performed, therefore, on her left eye. The histological evaluation of vitreous membrane revealed a complex immunophenotype (positivity for glial fibrillary acidic protein (GFAP), vimentin, S-100, anti-pan cytokeratin antibody (AE/AE3), and smooth muscle-specific actin (SMA) to various extents). The right eye remained unsymptomatic throughout this course. Besides being the first to analyze the tractional vitreoretinal membrane in IP with immunohistochemical methods, this case study points out that extreme cases of asymmetric side involvement in IP do exist, even to the point of one eye being completely unsymptomatic.
Open AccessImmunohistochemical Analysis of a Vitreous Membrane Removed from a Patient with Incontinentia Pigmenti-Related Retinal Detachment
This is a case history of a 23-year-old woman suffering from incontinentia pigmenti (IP). The patient’s vision in the left eye started to deteriorate due to cataract progression at the age of 22, and by the age of 23, it dropped from 0.9 to 0.04. Ultrasound examination confirmed tractional vitreoretinal membranes. Vitrectomy was performed, therefore, on her left eye. The histological evaluation of vitreous membrane revealed a complex immunophenotype (positivity for glial fibrillary acidic protein (GFAP), vimentin, S-100, anti-pan cytokeratin antibody (AE/AE3), and smooth muscle-specific actin (SMA) to various extents). The right eye remained unsymptomatic throughout this course. Besides being the first to analyze the tractional vitreoretinal membrane in IP with immunohistochemical methods, this case study points out that extreme cases of asymmetric side involvement in IP do exist, even to the point of one eye being completely unsymptomatic.
- Open Access
- 1 June 2019
- Published by Akademiai Kiado Zrt. in Imaging
- Vol. 106 (2) , 95-113
A multimodal pathway including the basal ganglia in the feline brain
The purpose of this paper is to give an overview of our present knowledge about the feline tecto-thalamo-basal ganglia cortical sensory pathway. We reviewed morphological and electrophysiological s...
- 1 June 2019
- Published by Akademiai Kiado Zrt. in Imaging
- Vol. 106 (2) , 95-113
Open AccessA multimodal pathway including the basal ganglia in the feline brain
The purpose of this paper is to give an overview of our present knowledge about the feline tecto-thalamo-basal ganglia cortical sensory pathway. We reviewed morphological and electrophysiological s...
- 1 March 2019
- Published by Elsevier in Physiology & Behavior
- Vol. 201, 70-82
Cognitive training improves the disturbed behavioral architecture of schizophrenia-like rats, “Wisket”
- 1 March 2019
- Published by Elsevier in Physiology & Behavior
- Vol. 201, 70-82
Cognitive training improves the disturbed behavioral architecture of schizophrenia-like rats, “Wisket”
- 1 September 2018
- Published by Elsevier in Autonomic Neuroscience
- Vol. 213, 34-42
Impaired pupillary control in “schizophrenia-like” WISKET rats
- 1 September 2018
- Published by Elsevier in Autonomic Neuroscience
- Vol. 213, 34-42
Impaired pupillary control in “schizophrenia-like” WISKET rats
- 27 July 2018
- Published by Wiley in Genes, Brain and Behavior
- Vol. 18 (4) , e12507
Impaired GAD1 expression in schizophrenia‐related WISKET rat model with sex‐dependent aggressive behavior and motivational deficit
After peri‐adolescence isolation rearing (IS) and subchronic ketamine (KET) treatment, adult, selectively bred Wistar rats (named WISKET) mimic abnormal behaviors reminiscent of human schizophrenia, including reduced prepulse‐inhibition of startle reflex, disturbances in cognition, locomotor activity and thermoregulation, decreased pain sensitivity and electrophysiological alterations. To further validate our WISKET rat line, regarding its translational utility in schizophrenia research, we examined their social behavior and introduced a short and simple holeboard (HB)‐like test to investigate their motivational deficit that predicts the cognitive disturbance. Sex‐dependent alterations in schizophrenia may yield important insights into its etiology; thus, male and female WISKET rats were also investigated and compared with their naive Wistar counterparts. Considering the contribution of the hippocampal and cortical GABAergic inhibitory circuitry in these behavioral alterations, molecular‐biology studies were also performed regarding the GAD1 gene products. Impaired social activity with increased aggression, stress‐related behavior, active social withdrawal, motivation deficit and decreased exploration were observed, especially in male WISKET rats, compared with Wistar ones and their corresponding females. These alterations were accompanied by sex‐dependent alterations regarding GAD67 mRNA and protein expression in the prefrontal cortex and hippocampus. In conclusion, the WISKET animals are valuable tools for animal‐based preclinical drug discovery studies for predictive screening of novel compounds improving negative symptoms with potential antipsychotic efficacy.
- 27 July 2018
- Published by Wiley in Genes, Brain and Behavior
- Vol. 18 (4) , e12507
Impaired GAD1 expression in schizophrenia‐related WISKET rat model with sex‐dependent aggressive behavior and motivational deficit
After peri‐adolescence isolation rearing (IS) and subchronic ketamine (KET) treatment, adult, selectively bred Wistar rats (named WISKET) mimic abnormal behaviors reminiscent of human schizophrenia, including reduced prepulse‐inhibition of startle reflex, disturbances in cognition, locomotor activity and thermoregulation, decreased pain sensitivity and electrophysiological alterations. To further validate our WISKET rat line, regarding its translational utility in schizophrenia research, we examined their social behavior and introduced a short and simple holeboard (HB)‐like test to investigate their motivational deficit that predicts the cognitive disturbance. Sex‐dependent alterations in schizophrenia may yield important insights into its etiology; thus, male and female WISKET rats were also investigated and compared with their naive Wistar counterparts. Considering the contribution of the hippocampal and cortical GABAergic inhibitory circuitry in these behavioral alterations, molecular‐biology studies were also performed regarding the GAD1 gene products. Impaired social activity with increased aggression, stress‐related behavior, active social withdrawal, motivation deficit and decreased exploration were observed, especially in male WISKET rats, compared with Wistar ones and their corresponding females. These alterations were accompanied by sex‐dependent alterations regarding GAD67 mRNA and protein expression in the prefrontal cortex and hippocampus. In conclusion, the WISKET animals are valuable tools for animal‐based preclinical drug discovery studies for predictive screening of novel compounds improving negative symptoms with potential antipsychotic efficacy.
- 1 July 2017
- Published by Elsevier in Neuroscience
- Vol. 356, 182-192
Background activity and visual responsiveness of caudate nucleus neurons in halothane anesthetized and in awake, behaving cats
- 1 July 2017
- Published by Elsevier in Neuroscience
- Vol. 356, 182-192
Background activity and visual responsiveness of caudate nucleus neurons in halothane anesthetized and in awake, behaving cats
- 1 February 2017
- Published by Elsevier in Physiology & Behavior
- Vol. 169, 155-164
Characterization of exploratory activity and learning ability of healthy and “schizophrenia-like” rats in a square corridor system (AMBITUS)
- 1 February 2017
- Published by Elsevier in Physiology & Behavior
- Vol. 169, 155-164
Characterization of exploratory activity and learning ability of healthy and “schizophrenia-like” rats in a square corridor system (AMBITUS)
- Open Access
The Development and Aging of the Magnocellular and Parvocellular Visual Pathways as Indicated by VEP Recordings between 5 and 84 Years of Age
It is well known that pattern reversal visual evoked potentials (VEPs) are age-sensitive. Through the use of this technique, it is possible to assess both of the major visual pathways (i.e., the magnocellular and parvocellular ones) in terms of function and development. What developmental path these pathways follow, and if they develop/age in parallel across the human lifespan is a matter of ongoing debate, yet, only a few VEP studies have dealt with this issue. This cross-sectional study examined a sample of 115 healthy volunteers aged 5 to 84 years. Beyond the standard checkerboard pattern reversal stimulation at 97% contrast, we recorded pattern-reversal VEPs at 6% contrast to selectively stimulate the M pathway and isoluminant red and green checkerboard stimulation was also used to selectively stimulate the P pathway. Our results do not support the developmental advantage of any of the pathways. The development of both pathways appear to take a remarkably long time (well into the 30s), and the signs of aging become marked over 50 years of age, especially in the case of the magnocellular pathway.
Open AccessThe Development and Aging of the Magnocellular and Parvocellular Visual Pathways as Indicated by VEP Recordings between 5 and 84 Years of Age
It is well known that pattern reversal visual evoked potentials (VEPs) are age-sensitive. Through the use of this technique, it is possible to assess both of the major visual pathways (i.e., the magnocellular and parvocellular ones) in terms of function and development. What developmental path these pathways follow, and if they develop/age in parallel across the human lifespan is a matter of ongoing debate, yet, only a few VEP studies have dealt with this issue. This cross-sectional study examined a sample of 115 healthy volunteers aged 5 to 84 years. Beyond the standard checkerboard pattern reversal stimulation at 97% contrast, we recorded pattern-reversal VEPs at 6% contrast to selectively stimulate the M pathway and isoluminant red and green checkerboard stimulation was also used to selectively stimulate the P pathway. Our results do not support the developmental advantage of any of the pathways. The development of both pathways appear to take a remarkably long time (well into the 30s), and the signs of aging become marked over 50 years of age, especially in the case of the magnocellular pathway.
- 1 July 2016
- Published by Elsevier in Behavioural Brain Research
- Vol. 307, 65-72
Electrophysiological alterations in a complex rat model of schizophrenia
- 1 July 2016
- Published by Elsevier in Behavioural Brain Research
- Vol. 307, 65-72
Electrophysiological alterations in a complex rat model of schizophrenia
- 1 September 2015
- Published by Elsevier in European Journal of Pharmacology
- Vol. 762, 158-164
In vivo potency of different ligands on voltage-gated sodium channels
- 1 September 2015
- Published by Elsevier in European Journal of Pharmacology
- Vol. 762, 158-164
In vivo potency of different ligands on voltage-gated sodium channels