| Genetic background of the hereditary spastic paraplegia phenotypes in Hungary—an analysis of 58 probands P Balicza, Z Grosz, MA Gonzalez, R Bencsik, K Pentelenyi, A Gal, E Varga, ... Journal of the neurological sciences 364, 116-121, 2016 | 38 | 2016 |
| 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 | 27 | 2018 |
| NKX2-1 New Mutation Associated with Myoclonus, Dystonia, Pituitary Dysfunction and Empty Sella P Balicza, Z Grosz, V Molnar, A Illés, D Csaban, A Gezsi, L Dezsi, ... Frontiers in Genetics 9, 335, 2018 | 21* | 2018 |
| NKX2-1 new mutation associated with myoclonus, dystonia, and pituitary involvement P Balicza, Z Grosz, V Molnár, A Illés, D Csabán, A Gézsi, L Dézsi, ... Frontiers in genetics 9, 2018 | 21 | 2018 |
| 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 |
| 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 | 4 | 2018 |
| Significance of whole exome sequencing in the diagnostics of rare neurological diseases-own experiences through a case presenting with ataxia P Balicza, Z Grosz, R Bencsik, A Illés, A Gál, A Gézsi, MJ Molnár Orvosi hetilap 159 (28), 1163-1169, 2018 | 2 | 2018 |
| Mitokondriális génmutáció igazolása dominálóan hipertrófiás cardiomyopathia képében megjelenő szisztémás kórképben= Identification of a mitochondrial gene mutation in a … A Tringer, Z Grosz, V Nagy, A Gál, B Csányi, L Hategan, J Borbás, ... Cardiologia Hungarica 47 (2), 135-138, 2017 | 1 | 2017 |
| Genetic and phenotypic characteristics of Hungarian patients with Neurodegeneration with Brain Iron Accumulation (NBIA) Z Grosz, R Bencsik, A Lengyel, A Gal, V Remenyi, G Tamas, P Klivenyi, ... EUROPEAN JOURNAL OF NEUROLOGY 22, 147-147, 2015 | 1 | 2015 |
| H20 Initiating and setting up a patient advocacy group for huntington’s disease in hungary Z Grosz, G Pék, G Báthori, JM Molnár J Neurol Neurosurg Psychiatry 89 (Suppl 1), A74-A75, 2018 | | 2018 |
| A teljesexom-szekvenálás jelentősége a ritka neurológiai betegségek diagnosztikájában–saját tapasztalatok egy ataxiás eset kapcsán P Balicza, Z Grosz, R Bencsik, A Illés, A Gál, A Gézsi, MJ Molnár Orvosi Hetilap 159 (28), 1163-1169, 2018 | | 2018 |
| Genomic studies in early onset Alzheimer's disease (EOAD) in Hungary D Csaban, R Bencsik, Z Grosz, B Antal, V Remenyi, BA Fekete, D Zadori, ... EUROPEAN JOURNAL OF NEUROLOGY 25, 95-95, 2018 | | 2018 |
| Genetic epidemiology analysis of Hungarian Charcot-Marie-Tooth patients GM Milley, Z Grosz, E Varga, NA Varga, J Boczan, Z Aranyi, P Dioszeghy, ... EUROPEAN JOURNAL OF NEUROLOGY 24, 606-606, 2017 | | 2017 |
| B28 Combined replication malfunctions in huntington’s disease Z Grosz, D Szirmai, V Reményi, R Bencsik, JM Molnár J Neurol Neurosurg Psychiatry 87 (Suppl 1), A19-A19, 2016 | | 2016 |
| differential diagnosis of hyperintense corticospinal tract lesions, detected in adult patients with spastic paraplegia: p21172 P Balicza, Z Grosz, G Lovas, P Barsi, G Rudas, A Lengyel, JM Molnar European Journal of Neurology 23, 431, 2016 | | 2016 |
| Assessing genetic risk factors for Alzheimer's disease in a Hungarian cohort Z Grosz, R Bencic, V Remenyi, D Csaban, B Szatmari, MJ Molnar EUROPEAN JOURNAL OF NEUROLOGY 23, 346-346, 2016 | | 2016 |
| genetic epidemiology analysis of Cx32 gene mutations in Hungary: p32256 GM Milley, A Gal, E Varga, Z Grosz, Z Aranyi, J Boczan, B Kalman, ... European Journal of Neurology 23, 878, 2016 | | 2016 |
| Genetic Background of the Hereditary Spastic Paraplegia Phenotypes in Hungary (P5. 049) M Molnar, P Balicza, Z Grosz, M Gonzalez, R Bencsik, K Pentelenyi, A Gal, ... Neurology 86 (16 Supplement), P5. 049, 2016 | | 2016 |
| Neurodegeneration and Brain Iron Accumulation disorders in Hungary: genotype-phenotype analysis (P7. 291) M Molnar, Z Grosz, R Bencsik, P Balicza, P Klivényi, G Tamás, P Acs, ... Neurology 84 (14 Supplement), P7. 291, 2015 | | 2015 |
| normal 0 21 Clinical evaluation of neurodegeneration with brain iron accumulation (nbia) due to Mpan in Hungary: Ep4126 Z Grosz, A Lengyel, A Gl, K Pentelenyi, Z Balogh, V Remenyi, JM Molnar European Journal of Neurology 21, 332, 2014 | | 2014 |
