Overview
Yuji Inaba practices in Azumino, Japan. Mr. Inaba is rated as an Advanced expert by MediFind in the treatment of Recessive Chondrodysplasia Punctata 1. His top areas of expertise are Recessive Chondrodysplasia Punctata 1, West Syndrome, Genetic Epilepsy with Febrile Seizures Plus (GEFS+), and Beta-Propeller Protein-Associated Neurodegeneration.
His clinical research consists of co-authoring 88 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Recessive Chondrodysplasia Punctata 1.
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.
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
- Beta-Propeller Protein-Associated Neurodegeneration
- Cytomegalic Inclusion DiseaseMr. Inaba isAdvanced. Learn about Cytomegalic Inclusion Disease.
- EncephalitisMr. Inaba isAdvanced. Learn about Encephalitis.
- Epilepsy in ChildrenMr. Inaba isAdvanced. Learn about Epilepsy in Children.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Recessive Chondrodysplasia Punctata 1
- Experienced
- Absence SeizureMr. Inaba isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeMr. Inaba isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AchondrogenesisMr. Inaba isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Inaba isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type