Overview
Ryosuke Bo practices practicing medicine in Kobe, Japan.
Mr. Bo is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Glutaric Acidemia Type 2, Mitochondrial Trifunctional Protein Deficiency, Mohr-Tranebjaerg Syndrome, and Gastrostomy.
He is actively involved in clinical research, co-authoring 43 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 Ryosuke Bo
Is Ryosuke Bo a top-rated expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Ryosuke Bo is classified as an Advanced expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, 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 Ryosuke Bo participate in research or clinical trials?
Yes. Ryosuke Bo has published 43 articles and abstracts on conditions like Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. You can view a list of Ryosuke Bo'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
- Glutaric Acidemia Type 2Mr. Bo isAdvanced. Learn about Glutaric Acidemia Type 2.
- Leigh SyndromeMr. Bo isAdvanced. Learn about Leigh Syndrome.
- Mitochondrial Trifunctional Protein Deficiency
- Mohr-Tranebjaerg SyndromeMr. Bo isAdvanced. Learn about Mohr-Tranebjaerg Syndrome.
- Primary Lateral SclerosisMr. Bo isAdvanced. Learn about Primary Lateral Sclerosis.
- Spinal Muscular Atrophy (SMA)
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Acute PancreatitisMr. Bo isExperienced. Learn about Acute Pancreatitis.
- Adrenoleukodystrophy (ALD)Mr. Bo isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Albright's Hereditary Osteodystrophy
- Becker Muscular DystrophyMr. Bo isExperienced. Learn about Becker Muscular Dystrophy.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- CitrullinemiaMr. Bo isExperienced. Learn about Citrullinemia.
- Classic GalactosemiaMr. Bo isExperienced. Learn about Classic Galactosemia.
- Cramp-Fasciculation SyndromeMr. Bo isExperienced. Learn about Cramp-Fasciculation Syndrome.
- Duchenne Muscular DystrophyMr. Bo isExperienced. Learn about Duchenne Muscular Dystrophy.
- Fructose-1,6-Bisphosphatase Deficiency
- Fukuyama Type Muscular Dystrophy
- GalactosemiaMr. Bo isExperienced. Learn about Galactosemia.
- GastrostomyMr. Bo isExperienced. Learn about Gastrostomy.
- Glutaric Acidemia Type 1Mr. Bo isExperienced. Learn about Glutaric Acidemia Type 1.
- Hereditary PancreatitisMr. Bo isExperienced. Learn about Hereditary Pancreatitis.
- Limb-Girdle Muscular DystrophyMr. Bo isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- LissencephalyMr. Bo isExperienced. Learn about Lissencephaly.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Low Blood SugarMr. Bo isExperienced. Learn about Low Blood Sugar.
- Muscle AtrophyMr. Bo isExperienced. Learn about Muscle Atrophy.
- Newborn Low Blood SugarMr. Bo isExperienced. Learn about Newborn Low Blood Sugar.
- Primary Carnitine DeficiencyMr. Bo isExperienced. Learn about Primary Carnitine Deficiency.
- PseudohypoparathyroidismMr. Bo isExperienced. Learn about Pseudohypoparathyroidism.
- RhabdomyolysisMr. Bo isExperienced. Learn about Rhabdomyolysis.
- Spinal Muscular Atrophy Type 2Mr. Bo isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Mr. Bo isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Undescended TesticleMr. Bo isExperienced. Learn about Undescended Testicle.
- Urea Cycle Disorders (UCD)Mr. Bo isExperienced. Learn about Urea Cycle Disorders (UCD).
- Von Gierke DiseaseMr. Bo isExperienced. Learn about Von Gierke Disease.
- Walker-Warburg SyndromeMr. Bo isExperienced. Learn about Walker-Warburg Syndrome.
- X-Linked Retinal DysplasiaMr. Bo isExperienced. Learn about X-Linked Retinal Dysplasia.