Overview
Takanori Hata practices practicing medicine in Chuo, Japan.
Mr. Hata is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Spastic Paraplegia Type 2, Spastic Paraplegia Type 7, Primary Lateral Sclerosis, and Myoclonic Epilepsy.
He is actively involved in clinical research, co-authoring 32 peer reviewed articles.
Gender
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 Takanori Hata
Is Takanori Hata a top-rated expert for Spastic Paraplegia Type 2?
MediFind is an objective health platform that identifies experts based on real-world data. Takanori Hata is classified as an Advanced expert for Spastic Paraplegia Type 2, 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 Takanori Hata participate in research or clinical trials?
Yes. Takanori Hata has published 32 articles and abstracts on conditions like Spastic Paraplegia Type 2. You can view a list of Takanori Hata'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
- Spastic Paraplegia Type 2Mr. Hata isAdvanced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Mr. Hata isAdvanced. Learn about Spastic Paraplegia Type 7.
- Experienced
- Amyotonia CongenitaMr. Hata isExperienced. Learn about Amyotonia Congenita.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- CamptocormismMr. Hata isExperienced. Learn about Camptocormism.
- Charcot-Marie-Tooth DiseaseMr. Hata isExperienced. Learn about Charcot-Marie-Tooth Disease.
- Congenital CataractMr. Hata isExperienced. Learn about Congenital Cataract.
- Dentatorubral-Pallidoluysian Atrophy
- Drug Induced DyskinesiaMr. Hata isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMr. Hata isExperienced. Learn about Dysarthria.
- Familial DysautonomiaMr. Hata isExperienced. Learn about Familial Dysautonomia.
- Familial Periodic ParalysisMr. Hata isExperienced. Learn about Familial Periodic Paralysis.
- Hereditary AtaxiaMr. Hata isExperienced. Learn about Hereditary Ataxia.
- Hypokalemic Periodic ParalysisMr. Hata isExperienced. Learn about Hypokalemic Periodic Paralysis.
- Lafora DiseaseMr. Hata isExperienced. Learn about Lafora Disease.
- Movement DisordersMr. Hata isExperienced. Learn about Movement Disorders.
- Multiple System AtrophyMr. Hata isExperienced. Learn about Multiple System Atrophy.
- Myasthenia GravisMr. Hata isExperienced. Learn about Myasthenia Gravis.
- Myoclonic EpilepsyMr. Hata isExperienced. Learn about Myoclonic Epilepsy.
- MyositisMr. Hata isExperienced. Learn about Myositis.
- Myotonia CongenitaMr. Hata isExperienced. Learn about Myotonia Congenita.
- Neuronal Intranuclear Inclusion Disease (NIID)
- NeurosarcoidosisMr. Hata isExperienced. Learn about Neurosarcoidosis.
- Neurotoxicity SyndromesMr. Hata isExperienced. Learn about Neurotoxicity Syndromes.
- Orthostatic HypotensionMr. Hata isExperienced. Learn about Orthostatic Hypotension.
- Primary Lateral SclerosisMr. Hata isExperienced. Learn about Primary Lateral Sclerosis.
- SpasticityMr. Hata isExperienced. Learn about Spasticity.
- Spinocerebellar AtaxiaMr. Hata isExperienced. Learn about Spinocerebellar Ataxia.
- Spinocerebellar Ataxia Type 31Mr. Hata isExperienced. Learn about Spinocerebellar Ataxia Type 31.