Overview
Ralph Deberardinis is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Deberardinis is rated as an Experienced provider by MediFind in the treatment of Chondrodystrophy. His top areas of expertise are Pyruvate Carboxylase Deficiency, Cerebral Hypoxia, Gliomatosis Cerebri, and N-Acetylglutamate Synthase Deficiency.
His clinical research consists of co-authoring 298 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 Chondrodystrophy.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INDEMNITY
- 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.
Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Scheuerle is rated as a Distinguished provider by MediFind in the treatment of Chondrodystrophy. Her top areas of expertise are Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.
Garrett Gotway is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Gotway is rated as an Advanced provider by MediFind in the treatment of Chondrodystrophy. His top areas of expertise are Polysyndactyly Cardiac Malformation, Nicolaides-Baraitser Syndrome, Snyder-Robinson Syndrome, and Fetal Akinesia Sequence.
University Of Texas Southwestern Medical Center At Dallas
Laura Mackay is a Pediatrics provider in Dallas, Texas. Dr. Mackay is rated as an Advanced provider by MediFind in the treatment of Chondrodystrophy. Her top areas of expertise are Isovaleric Acidemia, Beta-Ketothiolase Deficiency, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Wildervanck Syndrome.
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
- Pyruvate Carboxylase DeficiencyDr. Deberardinis isDistinguished. Learn about Pyruvate Carboxylase Deficiency.
- Advanced
- Cerebral HypoxiaDr. Deberardinis isAdvanced. Learn about Cerebral Hypoxia.
- Gliomatosis CerebriDr. Deberardinis isAdvanced. Learn about Gliomatosis Cerebri.
- Experienced
- Brachydactyly Mononen TypeDr. Deberardinis isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyDr. Deberardinis isExperienced. Learn about Chondrodystrophy.
- Familial Multiple LipomatosisDr. Deberardinis isExperienced. Learn about Familial Multiple Lipomatosis.
- Head and Neck Squamous Cell Carcinoma (HNSCC)Dr. Deberardinis isExperienced. Learn about Head and Neck Squamous Cell Carcinoma (HNSCC).
- HomocystinuriaDr. Deberardinis isExperienced. Learn about Homocystinuria.
- Increased Head CircumferenceDr. Deberardinis isExperienced. Learn about Increased Head Circumference.