Overview
Chiara Veredice practices in Rome, Italy. Ms. Veredice is highly rated in 6 conditions, according to our data. Her top areas of expertise are Hereditary Hyperekplexia, Cardiofaciocutaneous Syndrome, Dravet Syndrome, and Smith-Magenis Syndrome.
Her clinical research consists of co-authoring 28 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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.
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
- Advanced
- Cardiofaciocutaneous SyndromeMs. Veredice isAdvanced. Learn about Cardiofaciocutaneous Syndrome.
- Dravet SyndromeMs. Veredice isAdvanced. Learn about Dravet Syndrome.
- Epilepsy with Myoclonic-Atonic Seizures
- Hereditary HyperekplexiaMs. Veredice isAdvanced. Learn about Hereditary Hyperekplexia.
- Myoclonic EpilepsyMs. Veredice isAdvanced. Learn about Myoclonic Epilepsy.
- Smith-Magenis SyndromeMs. Veredice isAdvanced. Learn about Smith-Magenis Syndrome.
- Experienced
- Aplasia Cutis CongenitaMs. Veredice isExperienced. Learn about Aplasia Cutis Congenita.
- Batten DiseaseMs. Veredice isExperienced. Learn about Batten Disease.
- Brain AbscessMs. Veredice isExperienced. Learn about Brain Abscess.
- CDKL5 Deficiency DisorderMs. Veredice isExperienced. Learn about CDKL5 Deficiency Disorder.
- CLN1 DiseaseMs. Veredice isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Veredice isExperienced. Learn about CLN2 Disease.