Overview
Shobha Ramachandra practices practicing medicine in Mysore, India.
Their clinical expertise encompasses Biotinidase Deficiency, Inborn Amino Acid Metabolism Disorder, Multiple Carboxylase Deficiency, and Galactosemia.
They are actively involved in clinical research, co-authoring 13 peer reviewed articles.
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 Shobha C. Ramachandra
Is Shobha C. Ramachandra a top-rated expert for Biotinidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Shobha C. Ramachandra is classified as an Experienced expert for Biotinidase Deficiency, 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 Shobha C. Ramachandra participate in research or clinical trials?
Yes. Shobha C. Ramachandra has published 13 articles and abstracts on conditions like Biotinidase Deficiency. You can view a list of Shobha C. Ramachandra'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
- Biotinidase DeficiencyRamachandra isExperienced. Learn about Biotinidase Deficiency.
- Classic GalactosemiaRamachandra isExperienced. Learn about Classic Galactosemia.
- Congenital HypothyroidismRamachandra isExperienced. Learn about Congenital Hypothyroidism.
- Galactokinase DeficiencyRamachandra isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyRamachandra isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaRamachandra isExperienced. Learn about Galactosemia.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- HypothyroidismRamachandra isExperienced. Learn about Hypothyroidism.
- Inborn Amino Acid Metabolism DisorderRamachandra isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Multiple Carboxylase DeficiencyRamachandra isExperienced. Learn about Multiple Carboxylase Deficiency.
- Neonatal HypothyroidismRamachandra isExperienced. Learn about Neonatal Hypothyroidism.