J M. Fernandez-Ramos
Malaga, AN, Spain
Last Updated: 09/26/2026
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Found 16 publications
Epileptic and developmental encephalopathy secondary to inversion-duplication of chromosome 15: Description of epilepsy characteristics and therapeutic outcomes.
Journal: Epilepsia
Published: September 29, 2025
Delphi study on epidemiology, clinical management, disease burden, and treatment of paediatric patients with Duchenne muscular dystrophy in Spain.
Journal: Neurologia
Published: December 24, 2024
RYR1 myopathies in childhood: phenotype-genotype correlation and incidence
Journal: Revista de neurologia
Published: March 19, 2024
Debut and evolution MRI images of a child with a new genetic variant of vanishing white matter leukodystrophy
Journal: Revista de neurologia
Published: January 30, 2024
KIF1A gene-associated neurological disease: the correlation between genotype and phenotype
Journal: Revista de neurologia
Published: September 05, 2023
Congenital myotonia. Incidence and presentation of a series of cases
Journal: Revista de neurologia
Published: February 14, 2023
Joubert syndrome: incidence and clinicoradiological description of a genotyped series of seven cases
Joubert syndrome: incidence and clinicoradiological description of a genotyped series of seven cases
Journal: Revista de neurologia
Published: July 26, 2021
Epileptic status in paediatric patients: its developmental consequences and an epidemiological update
Journal: Revista de neurologia
Published: November 04, 2020
Ethylmalonic encephalopathy: phenotype-genotype description and review of its management.
Journal: Neurologia
Published: November 04, 2020
ADCY5-associated dyskinesia in young children: a case report of a family and an updated review
Journal: Revista de neurologia
Published: July 07, 2020
Infantile spinal atrophy: our experience in the last 25 years
Journal: Anales de pediatria (Barcelona, Spain : 2003)
Published: January 30, 2014
Last Updated: 09/26/2026