Overview
Masaru Shimura practices practicing medicine in Chiba, Japan.
Mr. Shimura is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Leigh Syndrome, Mitochondrial Complex 1 Deficiency, Citrullinemia, Urea Cycle Disorders (UCD), and Liver Transplant.
He is actively involved in clinical research, co-authoring 63 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 Masaru Shimura
Is Masaru Shimura a top-rated expert for Leigh Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Masaru Shimura is classified as an Distinguished expert for Leigh Syndrome, 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 Masaru Shimura participate in research or clinical trials?
Yes. Masaru Shimura has published 63 articles and abstracts on conditions like Leigh Syndrome. You can view a list of Masaru Shimura'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
- Leigh SyndromeMr. Shimura isDistinguished. Learn about Leigh Syndrome.
- Advanced
- CitrullinemiaMr. Shimura isAdvanced. Learn about Citrullinemia.
- Mitochondrial Complex 1 DeficiencyMr. Shimura isAdvanced. Learn about Mitochondrial Complex 1 Deficiency.
- Experienced
- Achalasia Microcephaly SyndromeMr. Shimura isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Adrenoleukodystrophy (ALD)Mr. Shimura isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Alpha ThalassemiaMr. Shimura isExperienced. Learn about Alpha Thalassemia.
- Andersen DiseaseMr. Shimura isExperienced. Learn about Andersen Disease.
- Bloom SyndromeMr. Shimura isExperienced. Learn about Bloom Syndrome.
- CACH SyndromeMr. Shimura isExperienced. Learn about CACH Syndrome.
- Cortical DysplasiaMr. Shimura isExperienced. Learn about Cortical Dysplasia.
- Cytochrome C Oxidase DeficiencyMr. Shimura isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Drug Induced DyskinesiaMr. Shimura isExperienced. Learn about Drug Induced Dyskinesia.
- Fabry DiseaseMr. Shimura isExperienced. Learn about Fabry Disease.
- Farber LipogranulomatosisMr. Shimura isExperienced. Learn about Farber Lipogranulomatosis.
- Fetal EdemaMr. Shimura isExperienced. Learn about Fetal Edema.
- Gaucher DiseaseMr. Shimura isExperienced. Learn about Gaucher Disease.
- HemochromatosisMr. Shimura isExperienced. Learn about Hemochromatosis.
- Hemolytic Disease of the NewbornMr. Shimura isExperienced. Learn about Hemolytic Disease of the Newborn.
- Hydrops FetalisMr. Shimura isExperienced. Learn about Hydrops Fetalis.
- Hypophosphatasia (HPP)Mr. Shimura isExperienced. Learn about Hypophosphatasia (HPP).
- Lactic AcidosisMr. Shimura isExperienced. Learn about Lactic Acidosis.
- Liver FailureMr. Shimura isExperienced. Learn about Liver Failure.
- Liver TransplantMr. Shimura isExperienced. Learn about Liver Transplant.
- MalnutritionMr. Shimura isExperienced. Learn about Malnutrition.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- MELAS SyndromeMr. Shimura isExperienced. Learn about MELAS Syndrome.
- Metabolic AcidosisMr. Shimura isExperienced. Learn about Metabolic Acidosis.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyMr. Shimura isExperienced. Learn about Microcephaly.
- Mitochondrial Trifunctional Protein Deficiency
- Optic Nerve AtrophyMr. Shimura isExperienced. Learn about Optic Nerve Atrophy.
- Pontocerebellar HypoplasiaMr. Shimura isExperienced. Learn about Pontocerebellar Hypoplasia.
- Protein DeficiencyMr. Shimura isExperienced. Learn about Protein Deficiency.
- Pyruvate Decarboxylase DeficiencyMr. Shimura isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Shimura isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- RhabdomyolysisMr. Shimura isExperienced. Learn about Rhabdomyolysis.
- Spinocerebellar AtaxiaMr. Shimura isExperienced. Learn about Spinocerebellar Ataxia.
- Striatonigral Degeneration InfantileMr. Shimura isExperienced. Learn about Striatonigral Degeneration Infantile.
- Tension HeadacheMr. Shimura isExperienced. Learn about Tension Headache.
- Urea Cycle Disorders (UCD)Mr. Shimura isExperienced. Learn about Urea Cycle Disorders (UCD).
- Wolff-Parkinson-White SyndromeMr. Shimura isExperienced. Learn about Wolff-Parkinson-White Syndrome.