person

Maria Mar O. G.

Country
Spain
Department
Servicio de Neuropediatria

Research Overview

Data & Insights

medical_services
Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
0
Sites with multiple studies

Has run more than one trial at 0 of 5 partner sites.

Specializations

Paediatric neurology and epilepsy

Clinical research in neurological disorders with a strong paediatric focus, including developmental and epileptic encephalopathies, partial-onset seizures, Dravet syndrome, Lennox-Gastaut syndrome, tuberous sclerosis complex, focal cortical dysplasia, and Rett syndrome.

  • Seizure disorders
  • Neurodevelopmental disorders
  • Autism spectrum disorders
  • Rare neurologic syndromes

Work in this area also extends to Angelman syndrome, GRIN-related neurodevelopmental disorder, and other complex childhood conditions affecting cognition, behaviour, and motor function.

Paediatric immunology and inflammatory disease

Active involvement in trials for atopic dermatitis, plaque psoriasis, psoriatic arthritis, juvenile idiopathic arthritis, systemic lupus erythematosus, Behçet’s disease, and chronic spontaneous urticaria.

  • Inflammatory skin disease
  • Autoimmune arthritis
  • Systemic autoimmune disease
  • Allergic and immune-mediated disorders

Her therapeutic interests include biologic therapy and targeted treatment strategies for persistent immune-mediated disease in children and adolescents.

Paediatric oncology and haematologic malignancy

Research activity includes acute lymphoblastic leukemia, acute myeloid leukemia, lymphoblastic lymphoma, neuroblastoma, glioma, medulloblastoma, Ewing sarcoma, and atypical teratoid/rhabdoid tumour.

  • Leukaemia
  • Lymphoma
  • Solid tumours
  • Central nervous system tumours

Her portfolio also includes relapsed and refractory malignancies and studies of novel immunotherapy and targeted oncology in paediatric populations.

Metabolic, genetic, and neuromuscular disorders

Clinical interests cover Duchenne muscular dystrophy, spinal muscular atrophy, Friedreich ataxia, Krabbe disease, mucopolysaccharidoses, Gaucher disease, Prader-Willi syndrome, and Angelman syndrome.

  • Inherited metabolic disease
  • Muscle and motor disorders
  • Lysosomal storage disorders
  • Gene therapy

This area also includes developmental genetic syndromes and rare childhood conditions linked to growth, movement, and neurocognitive impairment.

Paediatric respiratory, infectious, and cardiovascular disease

Additional trial involvement spans asthma, bronchopulmonary dysplasia, respiratory syncytial virus infection, COVID-19, serious bacterial infections, pulmonary arterial hypertension, heart failure, and hypertrophic cardiomyopathy.

  • Chronic airway disease
  • Paediatric infections
  • Pulmonary vascular disease
  • Cardiac dysfunction

Her research landscape also includes haematology, kidney disease, and immune-mediated complications seen in complex paediatric care.

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