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ELMIRA ELAHI, D.M.D
D.M.D
General Practice Dentistry
NPI: 1417135609Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
56753(CA)
Research & Publications (20)
Five quantitative trait loci control radiation-induced adenoma multiplicity in Mom1R Apc Min/+ mice.
PMID 19194513·PLoS One·2009
7-preclinical
Protein binding and metabolism influence the relative skin sensitization potential of cinnamic compounds.
PMID 15025500·Chem Res Toxicol·2004
7-preclinical
Determination of hepatitis C virus genotype by Pyrosequencing.
PMID 12711060·J Virol Methods·2003
8-other
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.
PMID 19353692·Mov Disord·2009
8-other
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma.
PMID 19656777·Hum Mol Genet·2009
8-other
R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family.
PMID 19087156·Eur J Neurol·2009
5-case
Bioemulsifier production by a halothermophilic Bacillus strain with potential applications in microbially enhanced oil recovery.
PMID 17876532·Biotechnol Lett·2008
8-other
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.
PMID 18513678·Am J Hum Genet·2008
8-other
Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol.
PMID 19096718·Mol Vis·2008
8-other
Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients.
PMID 17898270·Invest Ophthalmol Vis Sci·2007
8-other
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
PMID 17591938·J Mol Diagn·2007
4-observational
Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation.
PMID 17447113·J Bone Miner Metab·2007
8-other
Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.
PMID 16691202·J Invest Dermatol·2006
5-case
The role of lacrimal intubation in the management of facial trauma and tumor resection.
PMID 15923831·Plast Reconstr Surg·2005
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
- 24432 MUIRLANDS BLVD STE 123
LAKE FOREST, CA 92630 - Phone
- (949) 900-1740
Quick Facts
- NPI
- 1417135609
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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