Overview
Mahoko Furujo practices practicing medicine in Okayama, Japan.
Furujo is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Dihydropteridine Reductase Deficiency, Hypermethioninemia, Gaucher Disease Type 2, and Geleophysic Dysplasia.
They are actively involved in clinical research, co-authoring 20 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 Mahoko Furujo
Is Mahoko Furujo a top-rated expert for Dihydropteridine Reductase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Mahoko Furujo is classified as an Distinguished expert for Dihydropteridine Reductase 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 Mahoko Furujo participate in research or clinical trials?
Yes. Mahoko Furujo has published 20 articles and abstracts on conditions like Dihydropteridine Reductase Deficiency. You can view a list of Mahoko Furujo'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
- Distinguished
- Dihydropteridine Reductase Deficiency
- Advanced
- Gaucher Disease Type 2Furujo isAdvanced. Learn about Gaucher Disease Type 2.
- HypermethioninemiaFurujo isAdvanced. Learn about Hypermethioninemia.
- Experienced
- Acromicric DysplasiaFurujo isExperienced. Learn about Acromicric Dysplasia.
- Enlarged LiverFurujo isExperienced. Learn about Enlarged Liver.
- Geleophysic DysplasiaFurujo isExperienced. Learn about Geleophysic Dysplasia.
- Growth Hormone Deficiency (GHD)Furujo isExperienced. Learn about Growth Hormone Deficiency (GHD).
- HypopituitarismFurujo isExperienced. Learn about Hypopituitarism.
- Mucopolysaccharidoses (MPS)Furujo isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Neonatal HypothyroidismFurujo isExperienced. Learn about Neonatal Hypothyroidism.
- Pediatric Growth Hormone Deficiency
- Phenylketonuria (PKU)Furujo isExperienced. Learn about Phenylketonuria (PKU).
- Small for Gestational AgeFurujo isExperienced. Learn about Small for Gestational Age.
- SpasticityFurujo isExperienced. Learn about Spasticity.
- Turner SyndromeFurujo isExperienced. Learn about Turner Syndrome.