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ALICE SINGLETON, M.D.
M.D.
Pediatrics Physician
NPI: 1538232087Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
G25494(CA)
Research & Publications (20)
Using resident focus groups to improve subspecialty consultations in a pediatric urgent care setting.
PMID 17019915·J Natl Med Assoc·2006
8-other
Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplication.
PMID 14736756·Brain·2004
5-case
A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.
PMID 15254940·Mov Disord·2004
5-case
Clinical and neuropathological correlates of apolipoprotein E genotype in dementia with Lewy bodies.
PMID 12411758·Dement Geriatr Cogn Disord·2002
4-observational
Nitric oxide synthase gene polymorphisms in Alzheimer's disease and dementia with Lewy bodies.
PMID 11297817·Neurosci Lett·2001
8-other
Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation.
PMID 11099448·Brain·2000
5-case
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP.
PMID 18667258·Neurobiol Aging·2010
8-other
Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people.
PMID 19435741·Eur Heart J·2009
4-observational
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease.
PMID 19271249·Neurogenetics·2009
8-other
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.
PMID 19448620·Nat Genet·2009
8-other
Cardiac rhythm disturbance in a depressed patient after implantation with a vagus nerve stimulator.
PMID 19384253·J ECT·2009
5-case
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
PMID 19286695·Brain·2009
4-observational
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.
PMID 19303062·Am J Hum Genet·2009
8-other
Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.
PMID 19351622·J Med Genet·2009
8-other
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics.
PMID 19282984·PLoS Genet·2009
8-other
SNCA variants are associated with increased risk for multiple system atrophy.
PMID 19475667·Ann Neurol·2009
8-other
Parkinson's disease and low frequency alleles found together throughout LRRK2.
PMID 19489756·Ann Hum Genet·2009
8-other
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
PMID 19375058·Am J Hum Genet·2009
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 12021 WILMINGTON AVE
LOS ANGELES, CA 90059 - Phone
- (562) 427-5363
Quick Facts
- NPI
- 1538232087
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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