Overview
Gouri Passi-Rao practices practicing medicine in Indore, India.
Ms. Passi-Rao is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Recurrent Peripheral Facial Palsy, Guanidinoacetate Methyltransferase Deficiency, Inborn Amino Acid Metabolism Disorder, and Foot Drop.
She is actively involved in clinical research, co-authoring 28 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 Gouri R. Passi-Rao
Is Gouri R. Passi-Rao a top-rated expert for Recurrent Peripheral Facial Palsy?
MediFind is an objective health platform that identifies experts based on real-world data. Gouri R. Passi-Rao is classified as an Advanced expert for Recurrent Peripheral Facial Palsy, 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 Gouri R. Passi-Rao participate in research or clinical trials?
Yes. Gouri R. Passi-Rao has published 28 articles and abstracts on conditions like Recurrent Peripheral Facial Palsy. You can view a list of Gouri R. Passi-Rao'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
- Advanced
- Guanidinoacetate Methyltransferase Deficiency
- Recurrent Peripheral Facial PalsyMs. Passi-Rao isAdvanced. Learn about Recurrent Peripheral Facial Palsy.
- Experienced
- Absence SeizureMs. Passi-Rao isExperienced. Learn about Absence Seizure.
- Alternating Hemiplegia of ChildhoodMs. Passi-Rao isExperienced. Learn about Alternating Hemiplegia of Childhood.
- CACH SyndromeMs. Passi-Rao isExperienced. Learn about CACH Syndrome.
- CalcinosisMs. Passi-Rao isExperienced. Learn about Calcinosis.
- CysticercosisMs. Passi-Rao isExperienced. Learn about Cysticercosis.
- Drug Induced DyskinesiaMs. Passi-Rao isExperienced. Learn about Drug Induced Dyskinesia.
- EpilepsyMs. Passi-Rao isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenMs. Passi-Rao isExperienced. Learn about Epilepsy in Children.
- Facial ParalysisMs. Passi-Rao isExperienced. Learn about Facial Paralysis.
- Foot DropMs. Passi-Rao isExperienced. Learn about Foot Drop.
- Generalized Tonic-Clonic SeizureMs. Passi-Rao isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- HemiplegiaMs. Passi-Rao isExperienced. Learn about Hemiplegia.
- Inborn Amino Acid Metabolism DisorderMs. Passi-Rao isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- JaundiceMs. Passi-Rao isExperienced. Learn about Jaundice.
- Mononeuritis MultiplexMs. Passi-Rao isExperienced. Learn about Mononeuritis Multiplex.
- Movement DisordersMs. Passi-Rao isExperienced. Learn about Movement Disorders.
- Newborn JaundiceMs. Passi-Rao isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarMs. Passi-Rao isExperienced. Learn about Newborn Low Blood Sugar.
- Rathke Cleft CystMs. Passi-Rao isExperienced. Learn about Rathke Cleft Cyst.
- SarcoidosisMs. Passi-Rao isExperienced. Learn about Sarcoidosis.
- SeizuresMs. Passi-Rao isExperienced. Learn about Seizures.
- SpasticityMs. Passi-Rao isExperienced. Learn about Spasticity.
- Transient Familial HyperbilirubinemiaMs. Passi-Rao isExperienced. Learn about Transient Familial Hyperbilirubinemia.
- X-Linked Creatine DeficiencyMs. Passi-Rao isExperienced. Learn about X-Linked Creatine Deficiency.