person

Serrano Gimaré M.

Country
Spain
Department
200: Pediatric Neurology

Research Overview

Data & Insights

medical_services
Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
2
Sites with multiple studies

Has run more than one trial at 2 of 5 partner sites.

Specializations

Rare Genetic Disorders

The investigator specializes in treating rare genetic conditions, with particular emphasis on PMM2-CDG (Phosphomannomutase 2 - Congenital Disorder of Glycosylation) and its associated neurological manifestations.

  • Ataxia management in PMM2-CDG
  • Long-term therapeutic approaches
  • Novel treatment evaluation

The research focus includes assessment of innovative therapeutic interventions for patients with glycosylation disorders.

Neurological Disorders

Dedicated to advancing treatment options for Angelman Syndrome, focusing on cognitive function improvement and developmental progression in pediatric patients.

  • Cognitive function assessment
  • Developmental disorder therapeutics
  • Pediatric neurological conditions

The investigator evaluates novel therapeutic compounds targeting neurological symptom management in genetic disorders.

Clinical Pharmacology

Expertise in studying pharmacodynamics and pharmacokinetics of experimental treatments for rare genetic conditions.

  • Safety and tolerability assessment
  • Multiple-dose evaluation
  • Long-term therapeutic monitoring

The investigator conducts comprehensive evaluations of drug safety profiles across different age groups.

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