Overview
Chupong Ittiwut practices practicing medicine in Bangkok, Thailand.
Ittiwut is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Hereditary Ovalocytosis, Hereditary Elliptocytosis, Hereditary Pyropoikilocytosis, and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
They are actively involved in clinical research, co-authoring 53 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 Chupong Ittiwut
Is Chupong Ittiwut a top-rated expert for Hereditary Ovalocytosis?
MediFind is an objective health platform that identifies experts based on real-world data. Chupong Ittiwut is classified as an Advanced expert for Hereditary Ovalocytosis, 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 Chupong Ittiwut participate in research or clinical trials?
Yes. Chupong Ittiwut has published 53 articles and abstracts on conditions like Hereditary Ovalocytosis. You can view a list of Chupong 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
- Advanced
- Hereditary ElliptocytosisIttiwut isAdvanced. Learn about Hereditary Elliptocytosis.
- Hereditary OvalocytosisIttiwut isAdvanced. Learn about Hereditary Ovalocytosis.
- Hereditary Pyropoikilocytosis
- Experienced
- Absence SeizureIttiwut isExperienced. Learn about Absence Seizure.
- Acrokeratoelastoidosis of CostaIttiwut isExperienced. Learn about Acrokeratoelastoidosis of Costa.
- Acromicric DysplasiaIttiwut isExperienced. Learn about Acromicric Dysplasia.
- Acute Cerebellar AtaxiaIttiwut isExperienced. Learn about Acute Cerebellar Ataxia.
- Alternating Hemiplegia of Childhood
- AnemiaIttiwut isExperienced. Learn about Anemia.
- Blood ClotsIttiwut isExperienced. Learn about Blood Clots.
- Cerebrotendinous XanthomatosisIttiwut isExperienced. Learn about Cerebrotendinous Xanthomatosis.
- Coarctation of the AortaIttiwut isExperienced. Learn about Coarctation of the Aorta.
- Coffin-Siris SyndromeIttiwut isExperienced. Learn about Coffin-Siris Syndrome.
- Congenital Myasthenic SyndromeIttiwut isExperienced. Learn about Congenital Myasthenic Syndrome.
- Congenital Radioulnar SynostosisIttiwut isExperienced. Learn about Congenital Radioulnar Synostosis.
- Drug Induced DyskinesiaIttiwut isExperienced. Learn about Drug Induced Dyskinesia.
- Enlarged LiverIttiwut isExperienced. Learn about Enlarged Liver.
- EpilepsyIttiwut isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenIttiwut isExperienced. Learn about Epilepsy in Children.
- Fibrous DysplasiaIttiwut isExperienced. Learn about Fibrous Dysplasia.
- Focal DystoniaIttiwut isExperienced. Learn about Focal Dystonia.
- Focal Segmental Glomerulosclerosis
- Generalized Tonic-Clonic SeizureIttiwut isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Glanzmann ThrombastheniaIttiwut isExperienced. Learn about Glanzmann Thrombasthenia.
- Hallervorden-Spatz DiseaseIttiwut isExperienced. Learn about Hallervorden-Spatz Disease.
- HemiplegiaIttiwut isExperienced. Learn about Hemiplegia.
- Hemolytic AnemiaIttiwut isExperienced. Learn about Hemolytic Anemia.
- HypermethioninemiaIttiwut isExperienced. Learn about Hypermethioninemia.
- Immunodeficiency with Hyper IgM Type 1
- IntersexIttiwut isExperienced. Learn about Intersex.
- Lactic AcidosisIttiwut isExperienced. Learn about Lactic Acidosis.
- Limb-Girdle Muscular DystrophyIttiwut isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Mccune-Albright SyndromeIttiwut isExperienced. Learn about Mccune-Albright Syndrome.
- Metabolic AcidosisIttiwut isExperienced. Learn about Metabolic Acidosis.
- MicrognathiaIttiwut isExperienced. Learn about Micrognathia.
- Miller SyndromeIttiwut isExperienced. Learn about Miller Syndrome.
- Mucopolysaccharidoses (MPS)Ittiwut isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Ornithine Transcarbamylase Deficiency
- Osteitis FibrosaIttiwut isExperienced. Learn about Osteitis Fibrosa.
- Palmoplantar KeratodermaIttiwut isExperienced. Learn about Palmoplantar Keratoderma.
- Precocious PubertyIttiwut isExperienced. Learn about Precocious Puberty.
- Primary Immunodeficiency (PID)Ittiwut isExperienced. Learn about Primary Immunodeficiency (PID).
- RhabdomyolysisIttiwut isExperienced. Learn about Rhabdomyolysis.
- SeizuresIttiwut isExperienced. Learn about Seizures.
- Severe Congenital NeutropeniaIttiwut isExperienced. Learn about Severe Congenital Neutropenia.
- Spinocerebellar Degeneration and Corneal Dystrophy
- Urea Cycle Disorders (UCD)Ittiwut isExperienced. Learn about Urea Cycle Disorders (UCD).
- XanthomaIttiwut isExperienced. Learn about Xanthoma.