Overview
Prashant Warang practices practicing medicine in Mumbai, India.
Mr. Warang is highly rated in 13 conditions, according to our data. His clinical expertise encompasses Hereditary Methemoglobinemia, Methemoglobinemia, Autosomal Recessive Congenital Methemoglobinemia, and Hemolytic Anemia.
He is actively involved in clinical research, co-authoring 40 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 Prashant P. Warang
Is Prashant P. Warang a top-rated expert for Hereditary Methemoglobinemia?
MediFind is an objective health platform that identifies experts based on real-world data. Prashant P. Warang is classified as an Elite expert for Hereditary Methemoglobinemia, 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 Prashant P. Warang participate in research or clinical trials?
Yes. Prashant P. Warang has published 40 articles and abstracts on conditions like Hereditary Methemoglobinemia. You can view a list of Prashant P. Warang'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
- Elite
- Hereditary Methemoglobinemia
- Distinguished
- Autosomal Recessive Congenital Methemoglobinemia
- Hemolytic AnemiaMr. Warang isDistinguished. Learn about Hemolytic Anemia.
- MethemoglobinemiaMr. Warang isDistinguished. Learn about Methemoglobinemia.
- Advanced
- AnemiaMr. Warang isAdvanced. Learn about Anemia.
- Congenital Hemolytic AnemiaMr. Warang isAdvanced. Learn about Congenital Hemolytic Anemia.
- Dehydrated Hereditary Stomatocytosis
- Dyserythropoietic Anemia and Thrombocytopenia
- Glucose Phosphate Isomerase Deficiency
- Hereditary ElliptocytosisMr. Warang isAdvanced. Learn about Hereditary Elliptocytosis.
- Hereditary OvalocytosisMr. Warang isAdvanced. Learn about Hereditary Ovalocytosis.
- Hereditary SpherocytosisMr. Warang isAdvanced. Learn about Hereditary Spherocytosis.
- Phosphoglycerate Kinase Deficiency
- Experienced
- Aase SyndromeMr. Warang isExperienced. Learn about Aase Syndrome.
- Alpha ThalassemiaMr. Warang isExperienced. Learn about Alpha Thalassemia.
- Budd-Chiari SyndromeMr. Warang isExperienced. Learn about Budd-Chiari Syndrome.
- Cramp-Fasciculation SyndromeMr. Warang isExperienced. Learn about Cramp-Fasciculation Syndrome.
- Fetal EdemaMr. Warang isExperienced. Learn about Fetal Edema.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- HemoglobinopathyMr. Warang isExperienced. Learn about Hemoglobinopathy.
- HemolysisMr. Warang isExperienced. Learn about Hemolysis.
- Hemolytic Disease of the NewbornMr. Warang isExperienced. Learn about Hemolytic Disease of the Newborn.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Hydrops FetalisMr. Warang isExperienced. Learn about Hydrops Fetalis.
- Pure Red Cell AplasiaMr. Warang isExperienced. Learn about Pure Red Cell Aplasia.
- Pyruvate Kinase DeficiencyMr. Warang isExperienced. Learn about Pyruvate Kinase Deficiency.
- Sickle Cell DiseaseMr. Warang isExperienced. Learn about Sickle Cell Disease.
- SitosterolemiaMr. Warang isExperienced. Learn about Sitosterolemia.
- ThalassemiaMr. Warang isExperienced. Learn about Thalassemia.
- Transient Erythroblastopenia of Childhood