Daniel M. Mayoralas-Fernandez
Madrid, MD, Spain
Last Updated: 09/26/2026
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Found 33 publications
Computerized cognitive training as a treatment for ADHD: evidence summary and future directions
Journal: Medicina
Published: February 28, 2025
Early Severe Cortical Involvement and Novel FUCA1 Mutations in a Pediatric Fucosidosis Case.
Journal: Molecular genetics & genomic medicine
Published: May 26, 2024
Advancing the Understanding of Vesicle-Associated Membrane Protein 1-Related Congenital Myasthenic Syndrome: Phenotypic Insights, Favorable Response to 3,4-Diaminopyridine, and Clinical Characterization of Five New Cases.
Journal: Pediatric neurology
Published: November 20, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.
Journal: Nature communications
Published: September 01, 2023
Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings.
Journal: Neurocase
Published: March 07, 2022
A mild clinical and neuropsychological phenotype of Renpenning syndrome: A new case report with a maternally inherited PQBP1 missense mutation.
Journal: Applied neuropsychology. Child
Published: September 02, 2021
Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism.
Journal: Genes
Published: June 30, 2021
Last Updated: 09/26/2026