| Psychiatric symptoms of patients with primary mitochondrial DNA disorders G Inczedy-Farkas, V Remenyi, A Gal, Z Varga, P Balla, ... Behavioral and Brain Functions 8 (1), 9, 2012 | 73 | 2012 |
| Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients GM Milley, ET Varga, Z Grosz, C Nemes, Z Arányi, J Boczán, P Diószeghy, ... Neuromuscular Disorders 28 (1), 38-43, 2018 | 31 | 2018 |
| Analysis of GJB2 mutations and the clinical manifestation in a large Hungarian cohort N Kecskeméti, M Szönyi, A Gáborján, M Küstel, GM Milley, A Süveges, ... European Archives of Oto-Rhino-Laryngology 275 (10), 2441-2448, 2018 | 22 | 2018 |
| Comprehensive analysis of rare variants of 101 autism-linked genes in a Hungarian cohort of autism spectrum disorder patients P Balicza, NA Varga, B Bolgar, K Pentelenyi, R Bencsik, A Gal, A Gezsi, ... Frontiers in Genetics 10, 434, 2019 | 21 | 2019 |
| Natural and Induced Mitochondrial Phosphate Carrier Loss DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION EL Seifert, A Gál, MG Acoba, Q Li, L Anderson-Pullinger, T Golenár, ... Journal of Biological Chemistry 291 (50), 26126-26137, 2016 | 20 | 2016 |
| Localization of SUCLA2 and SUCLG2 subunits of succinyl CoA ligase within the cerebral cortex suggests the absence of matrix substrate-level phosphorylation in glial cells of … A Dobolyi, AG Bagó, A Gál, MJ Molnár, M Palkovits, V Adam-Vizi, ... Journal of bioenergetics and biomembranes 47 (1-2), 33-41, 2015 | 18 | 2015 |
| Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients GM Milley, ET Varga, Z Grosz, B Bereznai, Z Aranyi, J Boczan, ... Neuromuscular Disorders 26 (10), 706-711, 2016 | 11 | 2016 |
| Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases V Remenyi, G Inczedy-Farkas, K Komlosi, R Horvath, A Maasz, I Janicsek, ... Mitochondrial DNA 26 (4), 572-578, 2015 | 11 | 2015 |
| Dynamics of dystroglycan complex proteins and laminin changes due to angiogenesis in rat cerebral hypoperfusion EA Wappler, I Adorján, A Gál, P Galgóczy, K Bindics, Z Nagy Microvascular research 81 (2), 153-159, 2011 | 11 | 2011 |
| Maternally inherited diabetes mellitus, deafness, chronic progressive external ophthalmoplegia and myopathy as the result of A3243G mutation of mtDNA A Gál, A Szabó, K Pentelényi, Z Pál Orvosi hetilap 149 (34), 1593-1598, 2008 | 11 | 2008 |
| Genetically determined neuropathy (CMT 1A) accompanied by immune dysfunction: a case report Z Pál, E Kiss, A Gál, T Csépány, A Lengyel, MJ Molnar Inflammation Research 58 (7), 359-361, 2009 | 10 | 2009 |
| Cytoprotective effect of two synthetic enhancer substances,(−)-BPAP and (−)-deprenyl, on human brain capillary endothelial cells and rat PC12 cells L Denes, G Szilágyi, A Gál, Z Bori, Z Nagy Life sciences 79 (11), 1034-1039, 2006 | 9 | 2006 |
| Single, high-dose 17β-estradiol therapy has anti-apoptotic effect and induces cerebral plasticity following transient forebrain ischemia in gerbils E Wappler, A Gál, J Skopál, Z Nagy Acta Physiologica Hungarica 98 (2), 189-194, 2011 | 8 | 2011 |
| The effect of the CYP 2C19* 2 polymorphism on stroke care G Nyírő, G Inczédy-Farkas, V Reményi, A Gál, Z Pál, M Molnár Acta Physiologica Hungarica 99 (1), 33-39, 2012 | 7 | 2012 |
| Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women Z Pal, A Gal, V Remenyi, A Tordai, MJ Molnar Neuromuscular Disorders 19 (12), 822-824, 2009 | 6 | 2009 |
| Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen’s attitude P Balicza, A Terebessy, Z Grosz, NA Varga, A Gal, BA Fekete, MJ Molnar EPMA Journal 9 (1), 103-112, 2018 | 5 | 2018 |
| The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation [A PMP22 deléció módosító hatása EGR2 mutáció miatt Charcot … V Reményi, G Inczédy-Farkas, A Gál, B Bereznai, Z Pál, MJ Molnár IDEGGYÓGYÁSZATI SZEMLE/CLINICAL NEUROSCIENCE 67 (11-12), 420-425, 2014 | 5 | 2014 |
| MELAS syndrome mimicking somatoform disorder G Inczedy-Farkas, V Remenyi, A Meszaros, A Gal, G Blasko, B Bereznai, ... Open Medicine 6 (6), 758-761, 2011 | 5 | 2011 |
| Dynamics of dystroglycan-complex proteins and laminin immunoreactivities and expression due to angiogenesis in the rat brain following permanent bilateral carotid occlusion AE Wappler, I Adorján, A Gál, P Galgóczy, K Bindics, Z Nagy Microvasc Res 81, 153-9, 2011 | 5 | 2011 |
| Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature. A Gal, E Siska, Z Nagy, G Karpati, MJ Molnar Clinical neuropathology 27 (5), 289-294, 2008 | 5 | 2008 |
