Maria J. Molnar
Affiliations: | Semmelweis Egyetem, Hungary |
Area:
Neuroscience BiologyGoogle:
"Maria Molnar"Mean distance: 53433
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Publications
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| Jimoh IJ, Sebe B, Balicza P, et al. (2020) Wernicke-Korsakoff syndrome associated with mtDNA disease. Therapeutic Advances in Neurological Disorders. 13: 1756286420938972 |
| Molnár MJ, Borsos B, Várdi KV, et al. (2020) [The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]. Ideggyogyaszati Szemle. 73: 151-159 |
| Illés A, Balicza P, Gál A, et al. (2020) Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene Orvosi Hetilap. 161: 821-828 |
| Illés A, Csabán D, Grosz Z, et al. (2019) The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials. Frontiers in Genetics. 10: 1061 |
| Balicza P, Grosz Z, Molnár V, et al. (2018) NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement Frontiers in Genetics. 9: 335 |
| Kecskeméti N, Szönyi M, Gáborján A, et al. (2018) Analysis of GJB2 mutations and the clinical manifestation in a large Hungarian cohort. European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (Eufos) : Affiliated With the German Society For Oto-Rhino-Laryngology - Head and Neck Surgery |
| Beke A, Piko H, Haltrich I, et al. (2018) Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations. Bmc Medical Genetics. 19: 113 |
| Márki S, Göblös A, Szlávicz E, et al. (2018) The rs13388259 Intergenic Polymorphism in the Genomic Context of the Gene Is Associated with Parkinson's Disease in the Hungarian Population. Parkinson's Disease. 2018: 9351598 |
| Varga NÁ, Pentelényi K, Balicza P, et al. (2018) Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion Behavioral and Brain Functions. 14: 1-14 |
| Milley GM, Varga ET, Grosz Z, et al. (2018) Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients. Neuromuscular Disorders : Nmd. 28: 38-43 |