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DAVID STEVENSON, MD
MD
Neonatal-Perinatal Medicine Physician
NPI: 1558403790Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
G32668(CA)
Neonatal-Perinatal Medicine PhysicianPrimary
Pediatrics — Neonatal-Perinatal Medicine
Code: 2080N0001X
G32668(CA)
Research & Publications (20)
Beware of the weaker sex: don't get too close to your twin brother.
PMID 17766536·Pediatrics·2007
8-other
Ethical considerations in neuroimaging and its impact on decision-making for neonates.
PMID 12480489·Brain Cogn·2002
8-other
Sex differences in outcomes of very low birthweight infants: the newborn male disadvantage.
PMID 11040165·Arch Dis Child Fetal Neonatal Ed·2000
4-observational
Health-related quality of life measures in genetic disorders: an outcome variable for consideration in clinical trials.
PMID 19621444·Am J Med Genet C Semin Med Genet·2009
4-observational
Targeting nursing homes under the Quality Improvement Organization program's 9th statement of work.
PMID 19682119·J Am Geriatr Soc·2009
8-other
Aspirin sensitivity and desensitization for asthma and sinusitis.
PMID 19210906·Curr Allergy Asthma Rep·2009
6-review
Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1.
PMID 19461382·J Pediatr Orthop·2009
5-case
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography.
PMID 19118659·Bone·2009
8-other
Planning for the future--long-term care and the 2008 election.
PMID 18463373·N Engl J Med·2008
8-other
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement.
PMID 18559907·J Clin Endocrinol Metab·2008
5-case
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.
PMID 17666887·Genet Med·2007
6-review
Gastric rupture and necrosis in Prader-Willi syndrome.
PMID 17667731·J Pediatr Gastroenterol Nutr·2007
8-other
A novel multiple congenital anomaly-mental retardation syndrome with Pierre Robin sequence and cerebellar hypoplasia in two sisters.
PMID 17764080·Am J Med Genet A·2007
5-case
Differences in hospice care between home and institutional settings.
PMID 17985958·J Palliat Med·2007
4-observational
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster.
PMID 17431905·Am J Med Genet A·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 725 WELCH RD
PALO ALTO, CA 94304 - Phone
- (650) 497-8000
Quick Facts
- NPI
- 1558403790
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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