Distinguished in Prader-Willi Syndrome
Distinguished in Prader-Willi Syndrome
Lpch Medical Group Div Of Lucile
725 Welch Rd, 
Palo Alto, CA 

Overview

David Stevenson is a Medical Genetics specialist and a Pediatrics provider in Palo Alto, California. Dr. Stevenson is rated as a Distinguished provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Neurofibromatosis Type 1 (NF1), Neurofibromatosis, RASopathies, Costello Syndrome, and Deep Brain Stimulation.

His clinical research consists of co-authoring 157 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 8 articles and participated in 2 clinical trials in the study of Prader-Willi Syndrome.

Specialties
Medical Genetics
Pediatrics
Licenses
Pediatrics in CA
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Health Net

Accepted plan types not found. Please verify directly with the provider.

Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO

Locations

LPCH MEDICAL GROUP DIV OF LUCILE
725 Welch Rd, Palo Alto, CA 94304

Additional Areas of Focus

Dr. Stevenson has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.

Neurofibromatosis Type 1 (NF1)

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.


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Experienced in Prader-Willi Syndrome
Medical Genetics | Neonatology
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Medical Genetics | Neonatology
1 Daniel Burnham Ct, Suite 230c, 
San Francisco, CA 
 (27.8 miles away)
Languages Spoken:
English

James Goldberg is a Medical Genetics specialist and a Neonatologist in San Francisco, California. Dr. Goldberg is rated as an Experienced provider by MediFind in the treatment of Prader-Willi Syndrome. His top areas of expertise are Smith-Lemli-Opitz Syndrome, Fragile X Syndrome, Trisomy 13, and Chromosome 13q Duplication.

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.

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