Overview
Nicola Longo is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Longo is highly rated in 29 conditions, according to our data. His top areas of expertise are Primary Carnitine Deficiency, Gaucher Disease Type 1, Urea Cycle Disorders (UCD), and Phenylketonuria (PKU). Dr. Longo is currently accepting new patients.
His clinical research consists of co-authoring 137 peer reviewed articles and participating in 14 clinical trials. 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
- BridgeSpan
- Cigna
- SelectHealth
- Premera
- Regence
- UnitedHealthcare
Locations
10833 Le Conte Ave, Los Angeles, CA 90095
10833 Leconte Ave, Los Angeles, CA 90095
300 Medical Plz, Los Angeles, CA 90095
1 Breakthrough Way, Las Vegas, NV 89135
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.
14 Clinical Trials
Matthew Deardorff is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Deardorff is highly rated in 28 conditions, according to our data. His top areas of expertise are Cornelia De Lange Syndrome, Coffin-Siris Syndrome, Mosaicism, and Beckwith-Wiedemann Syndrome.
The Regents Of The University Of California
Deborah Krakow is a Medical Genetics specialist and an Obstetrics and Gynecologist in Los Angeles, California. Dr. Krakow has been practicing medicine for over 41 years is highly rated in 30 conditions, according to our data. Her top areas of expertise are Osteogenesis Imperfecta, Acromicric Dysplasia, Chondrodystrophy, and Spondylocarpotarsal Synostosis Syndrome.
Uc Regents Uci Dept Of Pediatrics
Virginia Kimonis is a Medical Genetics specialist and a Pediatrics provider in Orange, California. Dr. Kimonis is highly rated in 15 conditions, according to our data. Her top areas of expertise are Prader-Willi Syndrome, Pompe Disease, Hypotonia, Fabry Disease, and Hormone Replacement Therapy (HRT).
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.
- Distinguished
- Argininosuccinic Aciduria
- Classic Galactosemia
- Fabry Disease
- Galactose Epimerase Deficiency
- Galactosemia
- Gaucher Disease
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Arginase Deficiency
- Danon Disease
- Galactokinase Deficiency
- Inborn Amino Acid Metabolism Disorder
- Maternal Hyperphenylalaninemia
- Experienced
- Achalasia Microcephaly Syndrome
- Alpha Thalassemia
- Alternating Hemiplegia of Childhood
- Autism Spectrum Disorder
- Carnitine Palmitoyltransferase 1 Deficiency
- Citrullinemia