person

Otilia M.

Country
Romania
Department
Pediatrics III

Research Overview

Data & Insights

medical_services
Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
7
Sites with multiple studies

Has run more than one trial at 7 of 66 partner sites.

Specializations

Neurological Disorders

The investigator specializes in studying and treating Prader-Willi syndrome (PWS), a complex genetic disorder affecting various aspects of neurological and physical development.

  • Sleep-Wake Disorders
  • Genetic Neurological Conditions
  • Excessive Daytime Sleepiness

Current research focuses on evaluating novel therapeutic approaches for managing symptoms associated with PWS, particularly addressing sleep-related manifestations of the condition.

Sleep Medicine

The investigator has developed expertise in addressing sleep disorders specifically related to genetic conditions, with particular attention to excessive daytime sleepiness management.

  • Sleep Pattern Assessment
  • Wake-Promoting Interventions
  • Sleep-Wake Cycle Regulation

Their work encompasses comprehensive evaluation of sleep disturbances and their impact on quality of life in patients with rare genetic disorders.

Genetic Medicine

The investigator's work extends into understanding the genetic basis of complex neurological conditions and their manifestation in sleep-wake regulation.

  • Genetic Disorder Management
  • Symptom Assessment
  • Treatment Efficacy Evaluation

Their research contributes to advancing therapeutic strategies for managing symptoms in patients with genetically-based neurological disorders.

Related Investigators

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