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SUSAN HAGSTROM, M.D.
M.D.
Internal Medicine Physician
NPI: 1235112061IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
23438(AZ)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
GEISEL SCHOOL OF MEDICINE AT DARTMOUTH
Class of 1992
Research & Publications (20)
Assessing susceptibility to age-related macular degeneration with proteomic and genomic biomarkers.
PMID 19202148·Mol Cell Proteomics·2009
8-other
Sequence alterations in RX in patients with microphthalmia, anophthalmia, and coloboma.
PMID 19158959·Mol Vis·2009
8-other
Genetic analysis of complement factor H related 5, CFHR5, in patients with age-related macular degeneration.
PMID 19365580·Mol Vis·2009
8-other
Drug-eluting stents: patient understanding of the risks of premature cessation of antiplatelet drugs.
PMID 18834797·J Cardiothorac Vasc Anesth·2008
4-observational
Patient understanding of the importance of beta-blocker use in the perioperative period.
PMID 17544881·J Cardiothorac Vasc Anesth·2007
8-other
Interaction between the photoreceptor-specific tubby-like protein 1 and the neuronal-specific GTPase dynamin-1.
PMID 17525220·Invest Ophthalmol Vis Sci·2007
7-preclinical
High precision variational calculations for the Born-Oppenheimer energies of the ground state of the hydrogen molecule.
PMID 16526839·J Chem Phys·2006
8-other
Mutation screen of the cone-specific gene, CLUL1, in 376 patients with age-related macular degeneration.
PMID 17148042·Ophthalmic Genet·2006
8-other
Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.
PMID 16740911·J Med Genet·2006
5-case
Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.
PMID 16643894·Exp Eye Res·2006
8-other
An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome.
PMID 16024868·Br J Ophthalmol·2005
5-case
Tubby-like protein 1 (TULP1) interacts with F-actin in photoreceptor cells.
PMID 16303976·Invest Ophthalmol Vis Sci·2005
7-preclinical
SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.
PMID 16145681·Am J Med Genet A·2005
5-case
Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations.
PMID 16352475·Ophthalmic Genet·2005
4-observational
Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations.
PMID 14962443·Am J Ophthalmol·2004
5-case
Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation.
PMID 14702087·Nature·2004
8-other
A role for the Tubby-like protein 1 in rhodopsin transport.
PMID 11481257·Invest Ophthalmol Vis Sci·2001
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
- 5779 E MAYO BLVD
PHOENIX, AZ 85054 - Phone
- (480) 301-8000
Quick Facts
- NPI
- 1235112061
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 34
- Publications
- 20
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