Overview
Moin Vera is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Vera is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Mucopolysaccharidoses (MPS), Triple X Syndrome, and Chromosome 10q Deletion.
His clinical research consists of co-authoring 14 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- OTHER MEDICAID
- STATE MEDICAID
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.
Kaiser Permanente Los Angeles Medical Center - Genetics Department
Divya Vats is a Medical Genetics provider in Los Angeles, California. Dr. Vats is rated as an Advanced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Adrenoleukodystrophy (ALD), Classic Galactosemia, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Vats is currently accepting new patients.
Changrui Xiao is a Medical Genetics provider in Orange, California. Dr. Xiao is rated as an Advanced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Glutaric Acidemia Type 2, Retinopathy Pigmentary Mental Retardation, Adrenoleukodystrophy (ALD), and X-Linked Creatine Deficiency. Dr. Xiao is currently accepting new patients.
Robert Wallerstein is a Pediatrics specialist and a Medical Genetics provider in Monrovia, California. Dr. Wallerstein is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius, Pelizaeus-Merzbacher Disease, Leukodystrophy, and Farber Lipogranulomatosis.
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
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Distinguished
- Mucopolysaccharidoses (MPS)Dr. Vera isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Advanced
- Adrenoleukodystrophy (ALD)Dr. Vera isAdvanced. Learn about Adrenoleukodystrophy (ALD).
- Biotinidase DeficiencyDr. Vera isAdvanced. Learn about Biotinidase Deficiency.
- Chromosome 10q DeletionDr. Vera isAdvanced. Learn about Chromosome 10q Deletion.
- Classic GalactosemiaDr. Vera isAdvanced. Learn about Classic Galactosemia.
- Dihydropteridine Reductase Deficiency
- Kearns-Sayre SyndromeDr. Vera isAdvanced. Learn about Kearns-Sayre Syndrome.
- Experienced
- 2q37 Deletion SyndromeDr. Vera isExperienced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Vera isExperienced. Learn about 3MC Syndrome.
- 47 XYY SyndromeDr. Vera isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Vera isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Vera isExperienced. Learn about Abruzzo-Erickson Syndrome.
- AchondroplasiaDr. Vera isExperienced. Learn about Achondroplasia.