Back to Search
ELIZABETH IVES, M.D.
M.D.
Diagnostic Radiology Physician
NPI: 1265635056IndividualAccepts Medicare
Specialties, Licenses & Credentials
Diagnostic Radiology PhysicianPrimary
Radiology — Diagnostic Radiology
Code: 2085R0202X
C1-0009763(DE)MD424401(PA)25MA08917100(NJ)
CMS Specialties
PrimaryDIAGNOSTIC RADIOLOGY
Education
UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE
Class of 2001
Research & Publications (19)
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.
PMID 19107147·Eur J Hum Genet·2009
8-other
The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in Newfoundland.
PMID 18684116·Clin Genet·2008
8-other
Independent predictors of acute appendicitis on CT with pathologic correlation.
PMID 18620120·Acad Radiol·2008
8-other
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations.
PMID 17470132·Clin Genet·2007
8-other
Quantitative computed tomography perfusion of prostate cancer: correlation with whole-mount pathology.
PMID 16197611·Clin Prostate Cancer·2005
8-other
Effect of dutasteride therapy on Doppler US evaluation of prostate: preliminary results.
PMID 16183933·Radiology·2005
8-other
A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy.
PMID 15523628·Am J Med Genet A·2004
8-other
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
PMID 15447792·BMC Med Genet·2004
8-other
Modulation of IP(3)-sensitive Ca(2+) release by 2,3-butanedione monoxime.
PMID 12634934·Pflugers Arch·2003
7-preclinical
Familial articular hypermobility and scapho-trapezial/trapezoid osteoarthritis in two siblings.
PMID 12364650·Rheumatology (Oxford)·2002
5-case
Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome.
PMID 12019213·Hum Mol Genet·2002
8-other
A locus for autosomal dominant hereditary spastic ataxia, SAX1, maps to chromosome 12p13.
PMID 11774073·Am J Hum Genet·2002
8-other
Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.
PMID 11709538·Hum Mol Genet·2001
7-preclinical
Kyphomelic dysplasia: a rare form of semilethal skeletal dysplasia.
PMID 11140840·Clin Genet·2000
5-case
Biochemical and functional characterization of inositol 1,3,4,5, 6-pentakisphosphate 2-kinases.
PMID 10960485·J Biol Chem·2000
8-other
Older, hypertensive, and hypercholesterolemic fairgoers visit more booths and differ in their health concerns at a community health fair.
PMID 10941695·J Community Health·2000
8-other
A transcriptional insulator at the imprinted H19/Igf2 locus.
PMID 10921905·Genes Dev·2000
7-preclinical
Folate and vitamin B12 status of women in Newfoundland at their first prenatal visit.
PMID 10862228·CMAJ·2000
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
- 1 COOPER PLZ
CAMDEN, NJ 08103 - Phone
- (856) 342-2000
Quick Facts
- NPI
- 1265635056
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 25
- Publications
- 19
Are you this provider?
Claim Your Profile