Overview
Claudia Compagnucci practices practicing medicine in Rome, Italy.
Ms. Compagnucci is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Riboflavin Transporter Deficiency Neuronopathy, Primary Lateral Sclerosis, Adenylosuccinate Lyase Deficiency, and Hearing Loss.
She is actively involved in clinical research, co-authoring 47 peer reviewed articles.
Gender
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Claudia Compagnucci
Is Claudia Compagnucci a top-rated expert for Riboflavin Transporter Deficiency Neuronopathy?
MediFind is an objective health platform that identifies experts based on real-world data. Claudia Compagnucci is classified as an Distinguished expert for Riboflavin Transporter Deficiency Neuronopathy, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Claudia Compagnucci participate in research or clinical trials?
Yes. Claudia Compagnucci has published 47 articles and abstracts on conditions like Riboflavin Transporter Deficiency Neuronopathy. You can view a list of Claudia Compagnucci's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Riboflavin Transporter Deficiency NeuronopathyMs. Compagnucci isDistinguished. Learn about Riboflavin Transporter Deficiency Neuronopathy.
- Advanced
- Primary Lateral SclerosisMs. Compagnucci isAdvanced. Learn about Primary Lateral Sclerosis.
- Experienced
- Adenylosuccinate Lyase DeficiencyMs. Compagnucci isExperienced. Learn about Adenylosuccinate Lyase Deficiency.
- Drug Induced DyskinesiaMs. Compagnucci isExperienced. Learn about Drug Induced Dyskinesia.
- EpilepsyMs. Compagnucci isExperienced. Learn about Epilepsy.
- Focal or Multifocal Malformations in Neuronal Migration
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hearing LossMs. Compagnucci isExperienced. Learn about Hearing Loss.
- Hereditary AtaxiaMs. Compagnucci isExperienced. Learn about Hereditary Ataxia.
- HypotoniaMs. Compagnucci isExperienced. Learn about Hypotonia.
- Infantile Axonal NeuropathyMs. Compagnucci isExperienced. Learn about Infantile Axonal Neuropathy.
- LeukodystrophyMs. Compagnucci isExperienced. Learn about Leukodystrophy.
- ProgeriaMs. Compagnucci isExperienced. Learn about Progeria.
- Spinal Muscular Atrophy (SMA)Ms. Compagnucci isExperienced. Learn about Spinal Muscular Atrophy (SMA).