Overview
Thuong Ha practices practicing medicine in Adelaide, Australia.
Ha is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Seckel Syndrome, Aicardi Syndrome, RUNX1 Familial Platelet Disorder, and Knobloch Syndrome.
They are actively involved in clinical research, co-authoring 22 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 Thuong T. Ha
Is Thuong T. Ha a top-rated expert for Seckel Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Thuong T. Ha is classified as an Advanced expert for Seckel Syndrome, 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 Thuong T. Ha participate in research or clinical trials?
Yes. Thuong T. Ha has published 22 articles and abstracts on conditions like Seckel Syndrome. You can view a list of Thuong T. Ha'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
- Aicardi SyndromeHa isAdvanced. Learn about Aicardi Syndrome.
- Seckel SyndromeHa isAdvanced. Learn about Seckel Syndrome.
- Experienced
- Acromicric DysplasiaHa isExperienced. Learn about Acromicric Dysplasia.
- Autosomal Recessive Primary Microcephaly
- Brachydactyly Mononen Type
- Caffey DiseaseHa isExperienced. Learn about Caffey Disease.
- ChondrodystrophyHa isExperienced. Learn about Chondrodystrophy.
- Cortical DysplasiaHa isExperienced. Learn about Cortical Dysplasia.
- EncephaloceleHa isExperienced. Learn about Encephalocele.
- Knobloch SyndromeHa isExperienced. Learn about Knobloch Syndrome.
- Lennox-Gastaut Syndrome (LGS)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- Periventricular Heterotopia
- PolymicrogyriaHa isExperienced. Learn about Polymicrogyria.
- RhabdomyolysisHa isExperienced. Learn about Rhabdomyolysis.
- RUNX1 Familial Platelet Disorder
- Schwartz-Jampel Syndrome
- X-Linked Spondyloepiphyseal Dysplasia Tarda