ESTUDIO PERAD: ESTUDIO RETROSPECTIVO, MULTICÉNTRICO, OBSERVACIONAL Y NO INTERVENCIONISTA PARA VALORAR LA EFICACIA, TOLERABILIDAD E IMPACTO COGNITIVO DEL PERAMPANEL EN ADOLESCENTES EN LA PRÁCTICA CLÍNICA.

Datos básicos

Protocolo:: PAT-PER-2014-01 (Nº REGISTRO: 2015/0129)
EUDRACT:
NCT:
Centro:
Año de incio:
Año de finalización:: 2016

ESTUDIO OBSERVACIONAL

Documentos

No hay documentos

Participantes

Patricia Smeyers Dura

Investigador Principal

Financiadores - Promotores

PATRICIA SMEYERS DURA

Resultados del Ensayo Clínico

Publicaciones en Revistas 8

A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies.

Baumgartner T; (...); Sadowski K

Article. 10.1002/epi4.12459. 2021

Cannabidiol therapy for refractory epilepsy in paediatric real world setting: What's the benefit?

Smeyers, P.; (...); Hernandez, S.

Meeting Abstract. 2024

Cognitive adverse events of adjunctive eslicarbazepine acetate in children with refractory focal seizures

Smeyers, P.; (...); Gama, H.

Meeting Abstract. 2022

Cognitive and Behavioral Effects of Adjunctive Brivaracetam in Children and Adolescents with Focal Seizures: Final Data From an Open-label Follow-up Trial

Elshoff, Jan-Peer; (...); Smeyers, Patricia

Meeting Abstract. 10.1212/WNL.0000000000201877. 2023

Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene.

Marco-Hernández AV; (...); Martínez-Castellano F

Article. 10.1111/cge.14093. 2022

Papel del acetato de eslicarbazepina en el tratamiento de la epilepsia de origen focal en la edad pediátrica: consideraciones prácticas.

García-Peñas JJ; (...); Aparicio J

Review. 10.33588/rn.71s01.2020562. 2020

Severe Communication Delays Are Independent of Seizure Burden and Persist Despite Contemporary Treatments in SCN1A+ Dravet Syndrome: Insights from the ENVISION Natural History Study.

Perry, M. Scott; (...); Rico, Salvador

Article. 10.1111/epi.17850. 2023

Triplication of the PCDH19 Gene as a Novel Disease Mechanism Leading to Epileptic Encephalopathy Resembling Loss-of-Function Pathogenic Variants.

Gabaldón-Albero A; (...); Martínez F

Article. 10.3390/genes15101312. 2024