Overview
Benjamin Cocanougher is a Medical Genetics provider in Cincinnati, Ohio. Dr. Cocanougher is highly rated in 4 conditions, according to our data. His top areas of expertise are Galactose Epimerase Deficiency, Galactokinase Deficiency, Classic Galactosemia, and Galactosemia.
His clinical research consists of co-authoring 13 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
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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. Providers 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.
Children's Hospital Medical Center
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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
- Classic GalactosemiaDr. Cocanougher isAdvanced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyDr. Cocanougher isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Cocanougher isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Cocanougher isAdvanced. Learn about Galactosemia.
- Experienced
- Congenital Fiber-Type DisproportionDr. Cocanougher isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Tubular Aggregate MyopathyDr. Cocanougher isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular MyopathyDr. Cocanougher isExperienced. Learn about X-Linked Myotubular Myopathy.