Back to Search
MICHAEL D'URSO, MD
MD
Cardiovascular Disease Physician
NPI: 1699720631IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
4104(SD)
CMS Specialties
PrimaryCARDIOVASCULAR DISEASE (CARDIOLOGY)
Education
CREIGHTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1989
Research & Publications (20)
DDX11L: a novel transcript family emerging from human subtelomeric regions.
PMID 19476624·BMC Genomics·2009
7-preclinical
Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with Incontinentia Pigmenti.
PMID 19603533·Hum Mutat·2009
8-other
Exposure to pesticides residues from consumption of Italian blood oranges.
PMID 19680977·Food Addit Contam Part A Chem Anal Control Expo Risk Assess·2009
8-other
Phaseless imaging with experimental data: facts and challenges.
PMID 18157235·J Opt Soc Am A Opt Image Sci Vis·2008
8-other
Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations.
PMID 18350553·Hum Mutat·2008
7-preclinical
MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions.
PMID 17480217·BMC Med Genet·2007
8-other
Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.
PMID 17428316·BMC Med Genet·2007
5-case
Faithful non-linear imaging from only-amplitude measurements of incident and total fields.
PMID 19532625·Opt Express·2007
8-other
Functional characterization of the TMLH gene: promoter analysis, in situ hybridization, identification and mapping of alternative splicing variants.
PMID 17408883·Gene·2007
7-preclinical
Inverse scattering from phaseless measurements of the total field on open lines.
PMID 16985541·J Opt Soc Am A Opt Image Sci Vis·2006
8-other
Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction.
PMID 16239311·Hum Reprod·2006
5-case
Functional analysis of TMLH variants and definition of domains required for catalytic activity and mitochondrial targeting.
PMID 15754339·J Cell Physiol·2005
7-preclinical
Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activation.
PMID 15229184·Hum Mol Genet·2004
4-observational
Human synaptobrevin-like 1 gene basal transcription is regulated through the interaction of selenocysteine tRNA gene transcription activating factor-zinc finger 143 factors with evolutionary conserved cis-elements.
PMID 14672948·J Biol Chem·2004
7-preclinical
Characterization of the human STAT5A and STAT5B promoters: evidence of a positive and negative mechanism of transcriptional regulation.
PMID 15043997·FEBS Lett·2004
7-preclinical
Inverse scattering from phaseless measurements of the total field on a closed curve.
PMID 15078033·J Opt Soc Am A Opt Image Sci Vis·2004
8-other
Incontinentia pigmenti with NEMO mutation in a Turkish family.
PMID 15230896·Int J Dermatol·2004
5-case
Transcriptome analysis of mouse stem cells and early embryos.
PMID 14691545·PLoS Biol·2003
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4150 FIFTH STREET
RAPID CITY, SD 57701 - Phone
- (605) 399-4300
Quick Facts
- NPI
- 1699720631
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 37
- Publications
- 20
Are you this provider?
Claim Your Profile