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IVAN LOPEZ, M.D.
M.D.
Family Medicine Physician
NPI: 1992845069IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
036109448(IL)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 1994
Research & Publications (20)
Evidence for oxidative stress in the developing cerebellum of the rat after chronic mild carbon monoxide exposure (0.0025% in air).
PMID 19580685·BMC Neurosci·2009
7-preclinical
Tight coupling of the t-SNARE and calcium channel microdomains in adrenomedullary slices and not in cultured chromaffin cells.
PMID 17112584·Cell Calcium·2007
7-preclinical
Stem/progenitor cells in the postnatal inner ear of the GFP-nestin transgenic mouse.
PMID 15245756·Int J Dev Neurosci·2004
4-observational
Immunolocalization of voltage-gated calcium channel alpha1 subunits in the chinchilla cochlea.
PMID 12845523·Cell Tissue Res·2003
7-preclinical
A novel bifunctional phospholipase c that is regulated by Galpha 12 and stimulates the Ras/mitogen-activated protein kinase pathway.
PMID 11022047·J Biol Chem·2001
8-other
The calcimimetic AMG 641 accelerates regression of extraosseous calcification in uremic rats.
PMID 19321594·Am J Physiol Renal Physiol·2009
7-preclinical
Truncated aperture extrapolation for Fourier-based near-field acoustic holography by means of border-padding.
PMID 19507967·J Acoust Soc Am·2009
8-other
Immunohistochemical distribution of basement membrane proteins in the human inner ear from older subjects.
PMID 19348877·Hear Res·2009
8-other
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.
PMID 19268277·Am J Hum Genet·2009
7-preclinical
Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy.
PMID 19290534·Acta Neuropathol·2009
5-case
Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.
PMID 19586905·J Biol Chem·2009
7-preclinical
Direct upregulation of parathyroid calcium-sensing receptor and vitamin D receptor by calcimimetics in uremic rats.
PMID 19091789·Am J Physiol Renal Physiol·2009
7-preclinical
An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and Acadians.
PMID 18665195·Eur J Hum Genet·2009
8-other
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
PMID 19430481·Nat Genet·2009
7-preclinical
Histopathological and ultrastructural analysis of vestibular endorgans in Meniere's disease reveals basement membrane pathology.
PMID 19493357·BMC Ear Nose Throat Disord·2009
8-other
Disparities in the receipt of cardiac revascularization procedures between blacks and whites: an analysis of secular trends.
PMID 18646331·Ethn Dis·2008
8-other
Cystadenocarcinoma and leiomyoma in a peregrine falcon (Falco peregrinus brookei).
PMID 18587064·Vet Rec·2008
5-case
Hearing and balance screening and referrals for Medicare patients: a national survey of primary care physicians.
PMID 18669130·J Am Acad Audiol·2008
8-other
Human temporal bone consortium for research resource enhancement.
PMID 18364572·Otol Neurotol·2008
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
- 2003 MONTGOMERY RD, SUITE 106 107
AURORA, IL 60504 - Phone
- (630) 340-4211
Quick Facts
- NPI
- 1992845069
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 32
- Publications
- 20
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