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VATSALA RAMPRASAD, MD
MD
Pediatric Pulmonology Physician
NPI: 1306936604Individual
Specialties, Licenses & Credentials
Pediatric Pulmonology PhysicianPrimary
Pediatrics — Pediatric Pulmonology
Code: 2080P0214X
25MA04526300(NJ)MD038724L(PA)
Pediatric Sleep Medicine Physician
Pediatrics — Sleep Medicine
Code: 2080S0012X
25MA04526300(NJ)MD038724L(PA)
Research & Publications (12)
Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis.
PMID 18334959·Mol Vis·2008
5-case
Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.
PMID 18334947·Mol Vis·2008
8-other
Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: relevance of genetic testing and counseling.
PMID 17454743·Ophthalmic Genet·2007
8-other
Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.
PMID 17397048·Hum Mutat·2007
8-other
Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
PMID 17286451·Mol Diagn Ther·2007
8-other
Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
PMID 16288197·Mol Vis·2005
8-other
Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.
PMID 15623749·Invest Ophthalmol Vis Sci·2005
8-other
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.
PMID 18978954·Mol Vis·2008
8-other
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
PMID 18024964·Hum Mol Genet·2008
4-observational
Z-2 aldose reductase allele and diabetic retinopathy in India.
PMID 12660865·Ophthalmic Genet·2003
4-observational
Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients.
PMID 12081717·Clin Genet·2002
8-other
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
- 160 E ERIE AVE
PHILADELPHIA, PA 19134 - Phone
- (215) 427-5085
Quick Facts
- NPI
- 1306936604
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 2
- Publications
- 12
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