Overview
Nutan Kamath practices practicing medicine in Manipala, India.
Their clinical expertise encompasses Pseudoachondroplasia, Rhizomelic Syndrome, Multiple Carboxylase Deficiency, and Acanthosis Nigricans.
They are actively involved in clinical research, co-authoring 51 peer reviewed articles.
Locations
Bengaluru, KA, India
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 Nutan P. Kamath
Is Nutan P. Kamath a top-rated expert for Pseudoachondroplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Nutan P. Kamath is classified as an Experienced expert for Pseudoachondroplasia, 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 Nutan P. Kamath participate in research or clinical trials?
Yes. Nutan P. Kamath has published 51 articles and abstracts on conditions like Pseudoachondroplasia. You can view a list of Nutan P. Kamath'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
- Experienced
- Acanthosis NigricansKamath isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaKamath isExperienced. Learn about Achondroplasia.
- AnemiaKamath isExperienced. Learn about Anemia.
- Beta ThalassemiaKamath isExperienced. Learn about Beta Thalassemia.
- Brachydactyly Mononen TypeKamath isExperienced. Learn about Brachydactyly Mononen Type.
- CACH SyndromeKamath isExperienced. Learn about CACH Syndrome.
- Cerebral PalsyKamath isExperienced. Learn about Cerebral Palsy.
- ChondrodystrophyKamath isExperienced. Learn about Chondrodystrophy.
- Erythema NodosumKamath isExperienced. Learn about Erythema Nodosum.
- Familial HypertriglyceridemiaKamath isExperienced. Learn about Familial Hypertriglyceridemia.
- Gastrointestinal BleedingKamath isExperienced. Learn about Gastrointestinal Bleeding.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hearing LossKamath isExperienced. Learn about Hearing Loss.
- HistiocytosisKamath isExperienced. Learn about Histiocytosis.
- HypogonadismKamath isExperienced. Learn about Hypogonadism.
- Kawasaki DiseaseKamath isExperienced. Learn about Kawasaki Disease.
- MalnutritionKamath isExperienced. Learn about Malnutrition.
- Metabolic AcidosisKamath isExperienced. Learn about Metabolic Acidosis.
- Multiple Carboxylase DeficiencyKamath isExperienced. Learn about Multiple Carboxylase Deficiency.
- NephrocalcinosisKamath isExperienced. Learn about Nephrocalcinosis.
- Newborn JaundiceKamath isExperienced. Learn about Newborn Jaundice.
- Non-Langerhans-Cell Histiocytosis
- Pediatric MyocarditisKamath isExperienced. Learn about Pediatric Myocarditis.
- Primary HyperoxaluriaKamath isExperienced. Learn about Primary Hyperoxaluria.
- Propionic AcidemiaKamath isExperienced. Learn about Propionic Acidemia.
- PseudoachondroplasiaKamath isExperienced. Learn about Pseudoachondroplasia.
- ReticulohistiocytomaKamath isExperienced. Learn about Reticulohistiocytoma.
- Rhizomelic SyndromeKamath isExperienced. Learn about Rhizomelic Syndrome.
- Schwartz-Jampel SyndromeKamath isExperienced. Learn about Schwartz-Jampel Syndrome.
- SiderosisKamath isExperienced. Learn about Siderosis.
- SpasticityKamath isExperienced. Learn about Spasticity.
- ThalassemiaKamath isExperienced. Learn about Thalassemia.
- TonsillitisKamath isExperienced. Learn about Tonsillitis.
- Transient Familial Hyperbilirubinemia
- VasculitisKamath isExperienced. Learn about Vasculitis.
- Waardenburg SyndromeKamath isExperienced. Learn about Waardenburg Syndrome.
- Waardenburg Syndrome Type 1Kamath isExperienced. Learn about Waardenburg Syndrome Type 1.
- X-Linked HypophosphatemiaKamath isExperienced. Learn about X-Linked Hypophosphatemia.
- X-Linked Spondyloepiphyseal Dysplasia Tarda