Overview
Thomas Slavin is a Medical Genetics specialist and a Pediatrics provider in La Crescenta, California. Dr. Slavin is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Li-Fraumeni Syndrome, 1p36 Deletion Syndrome, Familial Colorectal Cancer, and Congenital Aplastic Anemia.
His clinical research consists of co-authoring 73 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
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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.
Richard Chang is a Medical Genetics provider in Orange, California. Dr. Chang is rated as a Distinguished provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Adrenoleukodystrophy (ALD), and Citrullinemia. Dr. Chang is currently accepting new 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 Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Adrenoleukodystrophy (ALD), Classic Galactosemia, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Vats is currently accepting new patients.
Walla Al-Hertani is a Medical Genetics provider in Orange, California. Dr. Al-Hertani is rated as an Advanced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Von Gierke Disease, Classic Galactosemia, Phosphoglycerate Mutase Deficiency, and Andersen Disease. Dr. Al-Hertani 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
- Advanced
- 1p36 Deletion SyndromeDr. Slavin isAdvanced. Learn about 1p36 Deletion Syndrome.
- Li-Fraumeni SyndromeDr. Slavin isAdvanced. Learn about Li-Fraumeni Syndrome.
- Experienced
- Congenital Aplastic AnemiaDr. Slavin isExperienced. Learn about Congenital Aplastic Anemia.
- Familial Adenomatous PolyposisDr. Slavin isExperienced. Learn about Familial Adenomatous Polyposis.
- Familial Colorectal CancerDr. Slavin isExperienced. Learn about Familial Colorectal Cancer.
- MosaicismDr. Slavin isExperienced. Learn about Mosaicism.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency