Navegar por autor "Couce Pico, María Luz"

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Gene Therapy for Neuronopathic Mucopolysaccharidoses: State of the Art

2021- De Castro López, María José; Del Toro, M.; Giugliani, R.; Couce Pico, María Luz
Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients

2019- Fernández Marmiesse, Ana; Roca Otero, Iria; Díaz-Flores, F.; Cantarín, V.; Pérez-Poyato, M. S.; [et al.]
Septo-optic dysplasia caused by a novel FLNA splice site mutation: a case report

2019- Fernández Marmiesse, Ana; Pérez-Poyato, M. S.; Fontalba, A.; Marco de Lucas, E.; Martínez, M. T.; [et al.]
The Consensus Definition of Bronchopulmonary Dysplasia Is an Adequate Predictor of Lung Function at Preschool Age

2022- Rite, S.; Martín de Vicente, C.; García-Iñiguez, J.P.; Couce Pico, María Luz; Samper, M.P.; [et al.]
Transcriptomic analysis of patients with clinical suspicion of maturity-onset diabetes of the young (MODY) with a negative genetic diagnosis

2022- Vázquez Mosquera, María Eugenia; González-Vioque, E.; Barbosa Gouveia, Sofía; Bellido Guerrero, Diego; Tejera Pérez, Cristina; [et al.]