Salvador Ibáñez Mico
Salvador Ibáñez Mico
Specialist Physician in Pediatrics and its Special Areas
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Murciamurcia
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Dr. Salvador Ibáñez trained in Pediatrics in Valencia and in 2008 joined the prestigious Neuropediatrics Unit at the Hospital Virgen de la Arrixaca in Murcia, where he completed his residency and continues to work. His expertise primarily encompasses patients with epilepsy, neurodevelopmental disorders (autism, language disorders, learning disabilities), and also metabolic and rare diseases. He has published numerous articles in international journals and is a member of the Sociedad Española de Neurología Pediátrica, the Sociedad Española de Epilepsia, the European Pediatric Neurology Society, and the Asociación Española de Errores Congénitos del Metabolismo (AECOM).
Key information
- Latest Publication:Association of mevalonate treatment and dietary intervention with neurological outcomes in children with encephalopathy
- Belongs to:Sociedad de Pediatría del Sureste
Professional Details
Hospital Quirónsalud Murcia
SPECIALIST PHYSICIAN PAEDIATRICS AND RELATED AREAS
January 2023
Hospital Virgen de la Arrixaca
Neuropediatra
January 2016
Hospital Universitario de Torrevieja
Neuropediatra
November 2006
Estudio
Licenciado en Medicina
universidad, Universidad Miguel Hernández
2001
Doctorado
Universidad de Murcia
2019
Formación Sanitaria Especializada
Especialidad en Pediatría y sus Áreas Específicas
hospital
Simposium sobre Deficiencia de la Decarboxilasa de Aminoácidos Aromáticos
Sociedad Española de Neurología Pediátrica
January 2021
IV Congreso Nacional sobre Enfermedades Raras
January 2018
1ª, 2ª y 4ª Jornada de Enfermedades de los Neurotransmisores
Asociación De Neu
January 2015
Stroke-like episodes in CDG: An international multicenter approach to discover the real phenotype, improve the diagnosis and management and understand the underlying mechanisms
Hospital Sant Joan de Déu
Proyecto Mitobase
CIBERER
International Working Group on Neurotransmitter Related Disorders (INTD)
Estudio sobre Deficiencia de Decarboxilasa de Aminoácidos Aromáticos (AADC) en pacientes pediátricos con patología neurológica
PTC Therapeuticals
TOLERABILITY AND EFFICACY OF L-SERINE IN PATIENTS WITH GRIN-RELATED ENCEPHALOPATHY
Hospital Sant Joan de Déu
Association of mevalonate treatment and dietary intervention with neurological outcomes in children with encephalopathy
Artículo
Brain M patterns in Inherited disorders of monoamine neurotransmitters: An analysis of 70 patients
Artículo
Congenital myasthenia and congenital disorders of glycosylation caused by mutations in the DPACT1 gene
Artículo
Diagnóstico y Tratamiento de las Enfermedades Metabólicas Hereditarias
Capítulo de libro
Dissecting the transcriptional program of phosphomannomutase 2 deficient cells: B-LCLs as a valuable model for congenital disorders of glycosylation studies
Artículo
Epilepsy in biotinidase deficiency after biotin treatment
Artículo
Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder
Artículo
Level of training in autistic spectrum disorders among hospital pediatricians
Artículo
Long-term prognosis of childhood absence epilepsy
Artículo
Mitochondrial DNA depletion syndrome-13: a case with an unusual onset
Artículo
Molecular characterization of Spanish patients with MECP2 duplication syndrome
Artículo
Oncogenic supnatosymelatonin as a biomarker of serotonin status in oligogenic amine-deficient patients
Artículo
Paradigmatic De Novo GRIN1 Variants Recapitulate pathophysiological Mechanisms Underlying GRIN1-Related Disorder Clinical Spectrum
Artículo
Radiological findings in methylmalonic acidemia
Artículo
Rapid-onset obesity with hypothalamic dysregulation, hypoventilation, and autonomic dysregulation (ROHHAD syndrome): A case report and literature review
Artículo
Rare Variants in 48 Genes Account for 42% of Cases Without Neurodevelopmental Delay in 246 Pediatric Patients
Artículo
Spanish translation, cross-cultural adaptation, and initial assessment of psychometric properties of the Lie In Childhood Epilepsy Questionnaire (QOLCE-16)
Artículo
The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1
Artículo
The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call
Artículo
Transition from child to adult epilepsy. Difficulties with an objective that cannot be delayed
Artículo
Volumetric study of brain MAL in a concert of patients with neurotransmitter disorders
Artículo
Sociedad de Pediatría del Sureste
European Pediatric Neurology Society
Sociedad Española de Epilepsia
Sociedad Española de Errores Congénitos del Metabolismo (AECOM)
Sociedad Española de Neurología Pediátrica
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Hospital Quirónsalud Murcia
Calle Miguel Hernández, 12
30011 Murcia
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