Overview
Linda Randolph is a Medical Genetics provider in Los Angeles, California. Dr. Randolph is rated as an Experienced provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. Her top areas of expertise are Neurofibromatosis, Chromosome 11 Uniparental Disomy, Chromosome 13q Duplication, and Trisomy 13.
Her clinical research consists of co-authoring 29 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- 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.
1 Clinical Trials
Jose Abdenur is a Medical Genetics provider in Orange, California. Dr. Abdenur is rated as an Advanced provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are Adrenoleukodystrophy (ALD), Von Gierke Disease, Glycogen Storage Disease Type 3, and Hyperlysinemia. Dr. Abdenur is currently accepting new patients.
Richard Chang is a Medical Genetics provider in Orange, California. Dr. Chang is rated as a Distinguished provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Adrenoleukodystrophy (ALD), and Citrullinemia. Dr. Chang is currently accepting new patients.
Raymond Wang is a Medical Genetics provider in Orange, California. Dr. Wang is rated as an Elite provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.
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
- 15q11.2 MicrodeletionDr. Randolph isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Randolph isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3p Deletion SyndromeDr. Randolph isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Randolph isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Randolph isAdvanced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Randolph isAdvanced. Learn about Abruzzo-Erickson Syndrome.
- Experienced
- Autism Spectrum DisorderDr. Randolph isExperienced. Learn about Autism Spectrum Disorder.
- Autosomal Cleft PalateDr. Randolph isExperienced. Learn about Autosomal Cleft Palate.
- Cantu SyndromeDr. Randolph isExperienced. Learn about Cantu Syndrome.
- ChondrodystrophyDr. Randolph isExperienced. Learn about Chondrodystrophy.
- Chromosome 13q DeletionDr. Randolph isExperienced. Learn about Chromosome 13q Deletion.
- Chromosome 2 Uniparental DisomyDr. Randolph isExperienced. Learn about Chromosome 2 Uniparental Disomy.