Overview
Yoichi Wada practices practicing medicine in Sendai, Japan.
Mr. Wada is highly rated in 9 conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Galactosemia, Galactokinase Deficiency, and Galactose Epimerase Deficiency.
He is actively involved in clinical research, co-authoring 26 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 Yoichi Wada
Is Yoichi Wada a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Yoichi Wada is classified as an Elite expert for Classic Galactosemia, 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 Yoichi Wada participate in research or clinical trials?
Yes. Yoichi Wada has published 26 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Yoichi Wada'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
- Elite
- Classic GalactosemiaMr. Wada isElite. Learn about Classic Galactosemia.
- Distinguished
- CitrullinemiaMr. Wada isDistinguished. Learn about Citrullinemia.
- Galactokinase DeficiencyMr. Wada isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Wada isDistinguished. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Wada isDistinguished. Learn about Galactosemia.
- Urea Cycle Disorders (UCD)Mr. Wada isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Argininosuccinic AciduriaMr. Wada isAdvanced. Learn about Argininosuccinic Aciduria.
- Glutaric Acidemia Type 2Mr. Wada isAdvanced. Learn about Glutaric Acidemia Type 2.
- Holocarboxylase Synthetase Deficiency
- Experienced
- Adrenoleukodystrophy (ALD)Mr. Wada isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Alternating Hemiplegia of ChildhoodMr. Wada isExperienced. Learn about Alternating Hemiplegia of Childhood.
- CataractMr. Wada isExperienced. Learn about Cataract.
- CholestasisMr. Wada isExperienced. Learn about Cholestasis.
- Congenital CataractMr. Wada isExperienced. Learn about Congenital Cataract.
- Diabetic KetoacidosisMr. Wada isExperienced. Learn about Diabetic Ketoacidosis.
- Folate DeficiencyMr. Wada isExperienced. Learn about Folate Deficiency.
- HemiplegiaMr. Wada isExperienced. Learn about Hemiplegia.
- JaundiceMr. Wada isExperienced. Learn about Jaundice.
- Low Blood SugarMr. Wada isExperienced. Learn about Low Blood Sugar.
- Maternal HyperphenylalaninemiaMr. Wada isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Metabolic AcidosisMr. Wada isExperienced. Learn about Metabolic Acidosis.
- Multiple Carboxylase DeficiencyMr. Wada isExperienced. Learn about Multiple Carboxylase Deficiency.
- Phenylketonuria (PKU)Mr. Wada isExperienced. Learn about Phenylketonuria (PKU).
- Propionic AcidemiaMr. Wada isExperienced. Learn about Propionic Acidemia.
- Pyruvate Decarboxylase DeficiencyMr. Wada isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Wada isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.