Overview
Rungnapa Ittiwut practices practicing medicine in Bangkok, Thailand.
Their clinical expertise encompasses Glanzmann Thrombasthenia, Severe Congenital Neutropenia, Ornithine Transcarbamylase Deficiency, and Blood Clots.
They are actively involved in clinical research, co-authoring 30 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 Rungnapa Ittiwut
Is Rungnapa Ittiwut a top-rated expert for Glanzmann Thrombasthenia?
MediFind is an objective health platform that identifies experts based on real-world data. Rungnapa Ittiwut is classified as an Experienced expert for Glanzmann Thrombasthenia, 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 Rungnapa Ittiwut participate in research or clinical trials?
Yes. Rungnapa Ittiwut has published 30 articles and abstracts on conditions like Glanzmann Thrombasthenia. You can view a list of Rungnapa Ittiwut'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
- AgranulocytosisIttiwut isExperienced. Learn about Agranulocytosis.
- Blood ClotsIttiwut isExperienced. Learn about Blood Clots.
- Congenital AfibrinogenemiaIttiwut isExperienced. Learn about Congenital Afibrinogenemia.
- Enlarged LiverIttiwut isExperienced. Learn about Enlarged Liver.
- Familial HypofibrinogenemiaIttiwut isExperienced. Learn about Familial Hypofibrinogenemia.
- Glanzmann ThrombastheniaIttiwut isExperienced. Learn about Glanzmann Thrombasthenia.
- Infantile NeutropeniaIttiwut isExperienced. Learn about Infantile Neutropenia.
- Lactic AcidosisIttiwut isExperienced. Learn about Lactic Acidosis.
- Limb-Girdle Muscular DystrophyIttiwut isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Macular Corneal Dystrophy Type 1Ittiwut isExperienced. Learn about Macular Corneal Dystrophy Type 1.
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Ornithine Transcarbamylase Deficiency
- Precocious PubertyIttiwut isExperienced. Learn about Precocious Puberty.
- Severe Congenital NeutropeniaIttiwut isExperienced. Learn about Severe Congenital Neutropenia.
- Urea Cycle Disorders (UCD)Ittiwut isExperienced. Learn about Urea Cycle Disorders (UCD).