Overview
Guney Bademci is a Medical Genetics provider in Miami, Florida. Dr. Bademci is rated as an Experienced provider by MediFind in the treatment of Galactose Epimerase Deficiency. His top areas of expertise are Branchiootorenal Syndrome, Branchio-Oculo-Facial Syndrome (BOFS), KBG Syndrome, and RASopathies. Dr. Bademci is currently accepting new patients.
His clinical research consists of co-authoring 76 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Galactose Epimerase Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
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.
University Of Miami
Willa Thorson is a Medical Genetics specialist and a Pediatrics provider in Miami, Florida. Dr. Thorson is rated as an Advanced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are CHARGE Syndrome, Classic Galactosemia, KBG Syndrome, and Galactosemia. Dr. Thorson is currently accepting new patients.
University Of Miami
Kumarie Latchman is a Medical Genetics provider in Miami, Florida. Dr. Latchman is rated as an Experienced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Classic Galactosemia, Early Infantile Epileptic Encephalopathy, Choanal Atresia, and Galactose Epimerase Deficiency. Dr. Latchman is currently accepting new patients.
University Of Miami
Deborah Barbouth is a Medical Genetics specialist and a Pediatrics provider in Miami, Florida. Dr. Barbouth is rated as an Advanced provider by MediFind in the treatment of Galactose Epimerase Deficiency. Her top areas of expertise are Gaucher Disease Type 1, Gaucher Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Splenectomy. Dr. Barbouth is currently accepting new patients.
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
- Branchio-Oculo-Facial Syndrome (BOFS)
- Branchiootorenal SyndromeDr. Bademci isElite. Learn about Branchiootorenal Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeDr. Bademci isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acromicric DysplasiaDr. Bademci isExperienced. Learn about Acromicric Dysplasia.
- AlbinismDr. Bademci isExperienced. Learn about Albinism.
- Classic GalactosemiaDr. Bademci isExperienced. Learn about Classic Galactosemia.
- ColobomaDr. Bademci isExperienced. Learn about Coloboma.
- Cortical DysplasiaDr. Bademci isExperienced. Learn about Cortical Dysplasia.