Ana Roche Martínez
Ayudante de investigación
Last Publications
- Xiol-Viñas C, Vidal-Falcó S, Pascual-Alonso A, Blasco-Perez L, Brandi-Tarrau N, Pacheco-Fernández P, Gerotina E, O'Callaghan-Gordo M, Pineda M and Armstrong-Moron J X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients. SCIENTIFIC REPORTS . 9(1): 11983-11983.
- Vidal-Falcó S, Brandi-Tarrau N, Pacheco-Fernández P, Gerotina E, Blasco-Perez L, Trotta JR, Derdak S, O'Callaghan-Gordo M, Garcia-Cazorla A, Pineda M and Armstrong-Moron J The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome. SCIENTIFIC REPORTS . 7(1): 12288-12288.
- Duarte ST, Armstrong-Moron J, Roche-Martinez A, Ortez-Gonzalez CI, Pérez A, O'Callaghan-Gordo M, Pereira A, Sanmartí F, Ormazabal-Herrero A, Artuch-Iriberri R, Pineda M and Garcia-Cazorla A Abnormal expression of cerebrospinal fluid cation chloride cotransporters in patients with Rett syndrome. PLoS One . 8(7): .
Projects
- Project name:
- Aproximaciones terapéuticas en un modelo célular de síndrome de Rett
- Leader
- MªAngels García Cazorla, Alfonso Luis De Oyarzabal Sanz, Alfonso Luis De Oyarzabal Sanz
- Funding entities:
- OSSJD - Obra Social Sant Joan de Déu
- Code
- Mi Princesa Rett
- Starting - finishing date:
- 2014 - 2024
- Project name:
- Síndrome de Rett
- Leader
- Judith Silvia Armstrong Morón
- Funding entities:
- Clientes Diversos
- Code
- General Rett
- Starting - finishing date:
- 2007 - 2024