Overview
Joonhong Park practices practicing medicine in Jeonju, Republic of Korea.
Park is highly rated in 5 conditions, according to our data. Their clinical expertise encompasses Hereditary Elliptocytosis, Hereditary Ovalocytosis, PIK3CA-Related Overgrowth Spectrum, and 15q11.2 Microdeletion.
They are actively involved in clinical research, co-authoring 181 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 Joonhong O. Park
Is Joonhong O. Park a top-rated expert for Hereditary Elliptocytosis?
MediFind is an objective health platform that identifies experts based on real-world data. Joonhong O. Park is classified as an Distinguished expert for Hereditary Elliptocytosis, 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 Joonhong O. Park participate in research or clinical trials?
Yes. Joonhong O. Park has published 181 articles and abstracts on conditions like Hereditary Elliptocytosis. You can view a list of Joonhong O. Park'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
- Distinguished
- Hereditary ElliptocytosisPark isDistinguished. Learn about Hereditary Elliptocytosis.
- Hereditary OvalocytosisPark isDistinguished. Learn about Hereditary Ovalocytosis.
- Advanced
- 15q11.2 MicrodeletionPark isAdvanced. Learn about 15q11.2 Microdeletion.
- Limb-Girdle Muscular Dystrophy Type 2B
- PIK3CA-Related Overgrowth Spectrum
- Experienced
- Acute Lymphoblastic Leukemia (ALL)
- Alpha ThalassemiaPark isExperienced. Learn about Alpha Thalassemia.
- AnemiaPark isExperienced. Learn about Anemia.
- Arthrogryposis Multiplex Congenita
- Atopic DermatitisPark isExperienced. Learn about Atopic Dermatitis.
- Atypical Hemolytic Uremic Syndrome (aHUS)
- Becker Muscular DystrophyPark isExperienced. Learn about Becker Muscular Dystrophy.
- Benign Autosomal Dominant Myopathy
- BlepharophimosisPark isExperienced. Learn about Blepharophimosis.
- Brown SyndromePark isExperienced. Learn about Brown Syndrome.
- CardiomyopathyPark isExperienced. Learn about Cardiomyopathy.
- CHARGE SyndromePark isExperienced. Learn about CHARGE Syndrome.
- Cholangiocarcinoma (Bile Duct Cancer)
- CholedocholithiasisPark isExperienced. Learn about Choledocholithiasis.
- Collagen VI-Related Myopathy
- Cone-Rod DystrophyPark isExperienced. Learn about Cone-Rod Dystrophy.
- Congenital ContracturesPark isExperienced. Learn about Congenital Contractures.
- Congenital Coronary Artery Malformation
- Congenital Fiber-Type Disproportion
- Congenital Hemolytic AnemiaPark isExperienced. Learn about Congenital Hemolytic Anemia.
- Congenital Myasthenic Syndrome
- Craniofrontonasal DysplasiaPark isExperienced. Learn about Craniofrontonasal Dysplasia.
- D-Minus Hemolytic Uremic Syndrome
- D-Plus Hemolytic Uremic Syndrome
- Dehydrated Hereditary Stomatocytosis
- DiarrheaPark isExperienced. Learn about Diarrhea.
- Dilated Cardiomyopathy (DCM)
- Duchenne Muscular DystrophyPark isExperienced. Learn about Duchenne Muscular Dystrophy.
- Emery-Dreifuss Muscular Dystrophy
- Enlarged LiverPark isExperienced. Learn about Enlarged Liver.
- EpilepsyPark isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenPark isExperienced. Learn about Epilepsy in Children.
- Familial Periodic ParalysisPark isExperienced. Learn about Familial Periodic Paralysis.
- Fetal EdemaPark isExperienced. Learn about Fetal Edema.
- Frontonasal DysplasiaPark isExperienced. Learn about Frontonasal Dysplasia.
- GallstonesPark isExperienced. Learn about Gallstones.
- Gastrointestinal Stromal Tumor
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- GigantismPark isExperienced. Learn about Gigantism.
- HemoglobinopathyPark isExperienced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaPark isExperienced. Learn about Hemolytic Anemia.
- Hemolytic Disease of the Newborn
- Hemolytic-Uremic SyndromePark isExperienced. Learn about Hemolytic-Uremic Syndrome.
- HepatitisPark isExperienced. Learn about Hepatitis.
- Hepatitis BPark isExperienced. Learn about Hepatitis B.
- Hereditary SpherocytosisPark isExperienced. Learn about Hereditary Spherocytosis.
- Horizontal Gaze Palsy with Progressive Scoliosis
- Hydrops FetalisPark isExperienced. Learn about Hydrops Fetalis.
- HyperthermiaPark isExperienced. Learn about Hyperthermia.
- HypotoniaPark isExperienced. Learn about Hypotonia.
- JaundicePark isExperienced. Learn about Jaundice.
- Leber Hereditary Optic Neuropathy (LHON)
- LeukodystrophyPark isExperienced. Learn about Leukodystrophy.
- Limb-Girdle Muscular Dystrophy
- Lupus NephritisPark isExperienced. Learn about Lupus Nephritis.
- Macular Corneal Dystrophy Type 1
- Marfan SyndromePark isExperienced. Learn about Marfan Syndrome.
- MicrotiaPark isExperienced. Learn about Microtia.
- Miyoshi MyopathyPark isExperienced. Learn about Miyoshi Myopathy.
- MosaicismPark isExperienced. Learn about Mosaicism.
- Moyamoya DiseasePark isExperienced. Learn about Moyamoya Disease.
- Noonan SyndromePark isExperienced. Learn about Noonan Syndrome.
- Parathyroid AdenomaPark isExperienced. Learn about Parathyroid Adenoma.
- Parathyroid HyperplasiaPark isExperienced. Learn about Parathyroid Hyperplasia.
- Paroxysmal Cold Hemoglobinuria
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Prader-Willi SyndromePark isExperienced. Learn about Prader-Willi Syndrome.
- Progressive External Ophthalmoplegia
- Pulmonary Valve StenosisPark isExperienced. Learn about Pulmonary Valve Stenosis.
- PustulesPark isExperienced. Learn about Pustules.
- Pyruvate Kinase DeficiencyPark isExperienced. Learn about Pyruvate Kinase Deficiency.
- RASopathiesPark isExperienced. Learn about RASopathies.
- Restrictive Cardiomyopathy (RCM)
- RosaceaPark isExperienced. Learn about Rosacea.
- SchizencephalyPark isExperienced. Learn about Schizencephaly.
- SeizuresPark isExperienced. Learn about Seizures.
- Sinus of Valsalva AneurysmPark isExperienced. Learn about Sinus of Valsalva Aneurysm.
- Sotos SyndromePark isExperienced. Learn about Sotos Syndrome.
- SplenomegalyPark isExperienced. Learn about Splenomegaly.
- Stomach CancerPark isExperienced. Learn about Stomach Cancer.
- ThalassemiaPark isExperienced. Learn about Thalassemia.
- ThrombocytopeniaPark isExperienced. Learn about Thrombocytopenia.
- Tubular Aggregate MyopathyPark isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Dominant Scapuloperoneal Myopathy
- X-Linked IchthyosisPark isExperienced. Learn about X-Linked Ichthyosis.
- X-Linked Myotubular Myopathy