Maria Adelaida García-Gimeno
Affiliations: | Universidad Politécnica de Valencia |
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| Moreno-Estellés M, Campos-Rodríguez Á, Rubio-Villena C, et al. (2023) Deciphering the Polyglucosan Accumulation Present in Lafora Disease Using an Astrocytic Cellular Model. International Journal of Molecular Sciences. 24 |
| Vela M, García-Gimeno MA, Sanchis A, et al. (2021) Neuroprotective Effect of IND1316, an Indole-Based AMPK Activator, in Animal Models of Huntington Disease. Acs Chemical Neuroscience |
| Brewer MK, Machio-Castello M, Viana R, et al. (2021) An empirical pipeline for personalized diagnosis of Lafora disease mutations. Iscience. 24: 103276 |
| Kumarasinghe L, Xiong L, Garcia-Gimeno MA, et al. (2021) TRIM32 and Malin in Neurological and Neuromuscular Rare Diseases. Cells. 10 |
| Perez-Jimenez E, Viana R, Muñoz-Ballester C, et al. (2020) Endocytosis of the glutamate transporter 1 is regulated by laforin and malin: Implications in Lafora disease. Glia |
| Sanz P, Garcia-Gimeno MA. (2020) Reactive Glia Inflammatory Signaling Pathways and Epilepsy. International Journal of Molecular Sciences. 21 |
| Espinós C, Galindo MI, García-Gimeno MA, et al. (2020) Oxidative Stress, a Crossroad Between Rare Diseases and Neurodegeneration. Antioxidants (Basel, Switzerland). 9 |
| Sanchis A, García-Gimeno MA, Cañada-Martínez AJ, et al. (2019) Metformin treatment reduces motor and neuropsychiatric phenotypes in the zQ175 mouse model of Huntington disease. Experimental & Molecular Medicine. 51: 65 |
| García-Gimeno MA, Knecht E, Sanz P. (2018) Lafora Disease: A Ubiquitination-Related Pathology. Cells. 7 |
| Garcia-Gimeno MA, Rodilla-Ramirez PN, Viana R, et al. (2018) A novel EPM2A mutation yields a slow progression form of Lafora disease. Epilepsy Research. 145: 169-177 |