Overview
George Diaz is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Diaz and is rated as a Distinguished provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Argininosuccinic Aciduria, Inborn Amino Acid Metabolism Disorder, and Ornithine Translocase Deficiency.
His clinical research consists of co-authoring 1 peer reviewed article. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Humana
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.
Kimihiko Oishi is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Oishi and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. His top areas of expertise are Micrognathia, Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and N-Acetylglutamate Synthase Deficiency.
Icahn School Of Medicine At Mount Sinai
Jaya Ganesh is a Medical Genetics specialist and a Pediatrics provider in New York, New York. Dr. Ganesh and is rated as an Advanced provider by MediFind in the treatment of 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. Her top areas of expertise are Fabry Disease, Pompe Disease, De Barsy Syndrome, and Multiple Sulfatase Deficiency.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Advanced
- Inborn Amino Acid Metabolism Disorder
- Ornithine Transcarbamylase Deficiency
- Ornithine Translocase Deficiency
- Urea Cycle Disorders (UCD)
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Arginase Deficiency
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Maple Syrup Urine Disease
- N-Acetylglutamate Synthase Deficiency
- Phenylketonuria (PKU)