Uliana Musokhranova Matveeva

Investigador post-doc

Research group

Nou-Fontanet L, Musokhranova U, Ramírez-Camacho A, Delgadillo V, Insuga VS, Fernández LA, Alonso-Colmenero I, Arzimanoglou A, Garcia-Cazorla A, De Oyarzabal-Sanz AL and Fons-Estupina C AFG2A-related encephalopathy: Effectiveness of ketogenic diet in epilepsy and mitochondrial dynamics modulation EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY 2025. 58: 20-26.
Illescas S, Díaz-Osorio Y, Serradell A, Toro-Soria L, Musokhranova U, Julià-Palacios NA, Ribeiro J, Altafaj X, Olivella M, O'Callaghan-Gordo M, Darling A, Armstrong-Moron J, Artuch-Iriberri R, Garcia-Cazorla A and De Oyarzabal-Sanz AL Metabolic characterization of neurogenetic disorders involving glutamatergic neurotransmission JOURNAL OF INHERITED METABOLIC DISEASE 2024. 47(3): 551-569.
Musokhranova U, Grau-Páez C, Vergara C, Rodríguez-Pascau L, Xiol-Viñas C, Castells AA, Alcántara S, Rodríguez-Pombo P, Pizcueta P, Martinell M, Garcia-Cazorla A and De Oyarzabal-Sanz AL Mitochondrial modulation with leriglitazone as a potential treatment for Rett syndrome JOURNAL OF TRANSLATIONAL MEDICINE 2023. 21(1): 756-756.

More Publications

Project name:: Modelos experimentales de sinaptopatías aplicados a la medicina personalizada de trastornos genéticos raros de la comunicación neuronal neuropediátricos
Leader: MªAngels García Cazorla, Alfonso Luis De Oyarzabal Sanz
Funding entities:: Instituto de Salud Carlos III (ISCIII)
Code: PI24/00469
Starting - finishing date:: 2024 - 2027

Project name:: Sinapsis en un chip: medicina personalizada en trastornos genéticos del neurodesarrollo que afectan a la comunicación sináptica
Leader: MªAngels García Cazorla
Funding entities:: Instituto de Salud Carlos III (ISCIII)
Code: PI21/00073
Starting - finishing date:: 2022 - 2025

Project name:: Medicina personalizada en los defectos genéticos de la neurotransmisión en pediatría. Nuevo enfoque basado en el metabolismo de la sinapsis neuronal
Leader: MªAngels García Cazorla
Funding entities:: Instituto de Salud Carlos III (ISCIII)
Code: PI18/00111
Starting - finishing date:: 2019 - 2022

More projects

Nanomedicine to tackle rare diseases
Wednesday, 28 February 2024
Experts in nanomedicine from various fields have gathered today for the fifth consecutive year at Nano Rare Diseases Day. This event is co-organized by IRSJD and the NANOMED Spain platform, coordinated by IBEC.
Advances in Research on Rett Syndrome
Friday, 24 November 2023
A study conducted by the Paediatric Neurometabolic Disorders: Neural Communication Mechanisms and Personalised Therapies Group at IRSJD · SJD Barcelona Children's Hospital confirms mitochondrial dysfunction in two distinct models of Rett syndrome, highlighting the significance of distinguishing between brain regions and stages of the disease. The findings of this study open up new avenues for treatment development.

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