Salvador Mico-Ibanez
Murcia, MU, Spain
Last Updated: 09/26/2026
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Found 34 publications
Pediatric developmental epileptic encephalopathies treated with cenobamate: Real-world outcomes across etiologies, syndromes, and seizure types.
Journal: Epilepsia
Published: June 26, 2026
Correction: Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy.
Journal: Frontiers in cell and developmental biology
Published: March 06, 2026
Epileptic and developmental encephalopathy secondary to inversion-duplication of chromosome 15: Description of epilepsy characteristics and therapeutic outcomes.
Journal: Epilepsia
Published: September 29, 2025
Genotype-phenotype correlations and putative modifier genes in SYNGAP1 Encephalopathy.
Journal: Neurobiology of disease
Published: September 15, 2025
Real-world use of cenobamate in pediatric focal epilepsies and developmental epileptic encephalopathies: A multicenter retrospective series.
Journal: Epilepsia
Published: May 13, 2025
A Multi-Target Pharmacological Correction of a Lipoyltransferase LIPT1 Gene Mutation in Patient-Derived Cellular Models.
Journal: Antioxidants (Basel, Switzerland)
Published: July 19, 2024
Effect of a physical exercise program supported by wearable technology in children with drug-resistant epilepsy. A randomized controlled trial.
Journal: Seizure
Published: April 26, 2024
Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Journal: European journal of human genetics : EJHG
Published: February 15, 2024
Cross-cultural validation and psychometric properties of the Spanish version of the quality of life in Childhood epilepsy Questionnaire (QOLCE-55).
Journal: Epilepsy & behavior : E&B
Published: November 12, 2023
Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy.
Journal: Frontiers in cell and developmental biology
Published: October 13, 2023
A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Journal: European journal of human genetics : EJHG
Published: September 22, 2023
Sotos Syndrome and Nephrocalcinosis a Rare But Possible Association Due to Impact on Contiguous Genes
Journal: Journal of clinical research in pediatric endocrinology
Published: August 10, 2023
Last Updated: 09/26/2026