Overview
Kottayam Radhakrishnan practices practicing medicine in Melbourne, Australia.
Their clinical expertise encompasses MYH9 Related Thrombocytopenia, Anemia, Dehydrated Hereditary Stomatocytosis, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
They are actively involved in clinical research, co-authoring 11 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 Kottayam Radhakrishnan
Is Kottayam Radhakrishnan a top-rated expert for MYH9 Related Thrombocytopenia?
MediFind is an objective health platform that identifies experts based on real-world data. Kottayam Radhakrishnan is classified as an Experienced expert for MYH9 Related Thrombocytopenia, 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 Kottayam Radhakrishnan participate in research or clinical trials?
Yes. Kottayam Radhakrishnan has published 11 articles and abstracts on conditions like MYH9 Related Thrombocytopenia. You can view a list of Kottayam Radhakrishnan'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
- Alpha ThalassemiaRadhakrishnan isExperienced. Learn about Alpha Thalassemia.
- AnemiaRadhakrishnan isExperienced. Learn about Anemia.
- Congenital Hemolytic AnemiaRadhakrishnan isExperienced. Learn about Congenital Hemolytic Anemia.
- Dehydrated Hereditary StomatocytosisRadhakrishnan isExperienced. Learn about Dehydrated Hereditary Stomatocytosis.
- DehydrationRadhakrishnan isExperienced. Learn about Dehydration.
- Dyserythropoietic Anemia and ThrombocytopeniaRadhakrishnan isExperienced. Learn about Dyserythropoietic Anemia and Thrombocytopenia.
- Fetal EdemaRadhakrishnan isExperienced. Learn about Fetal Edema.
- Hemolytic AnemiaRadhakrishnan isExperienced. Learn about Hemolytic Anemia.
- Hemolytic Disease of the NewbornRadhakrishnan isExperienced. Learn about Hemolytic Disease of the Newborn.
- Hemophagocytic LymphohistiocytosisRadhakrishnan isExperienced. Learn about Hemophagocytic Lymphohistiocytosis.
- HistiocytosisRadhakrishnan isExperienced. Learn about Histiocytosis.
- Hydrops FetalisRadhakrishnan isExperienced. Learn about Hydrops Fetalis.
- MYH9 Related ThrombocytopeniaRadhakrishnan isExperienced. Learn about MYH9 Related Thrombocytopenia.
- Non-Langerhans-Cell HistiocytosisRadhakrishnan isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Paroxysmal Cold HemoglobinuriaRadhakrishnan isExperienced. Learn about Paroxysmal Cold Hemoglobinuria.
- Paroxysmal Nocturnal Hemoglobinuria (PNH)Radhakrishnan isExperienced. Learn about Paroxysmal Nocturnal Hemoglobinuria (PNH).
- ReticulohistiocytomaRadhakrishnan isExperienced. Learn about Reticulohistiocytoma.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency