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MARY GENTILE, DO
DO
Family Medicine Physician
NPI: 1861480998IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
39870(CO)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 1992
Research & Publications (20)
Beta-amyloid deposition in brain is enhanced in mouse models of arterial hypertension.
PMID 17673335·Neurobiol Aging·2009
7-preclinical
Prompt and sustained response of a steroid-refractory autoimmune hemolytic anemia to a rituximab-based therapy in a chronic lymphocytic leukemia patient.
PMID 18064461·Cancer Chemother Pharmacol·2008
5-case
Small dense LDL particles and metabolic syndrome in a sample of middle-aged women. Findings from Progetto Atena.
PMID 18035055·Clin Chim Acta·2008
8-other
Efficacy of inpatient treatment in severely malnourished anorexia nervosa patients.
PMID 19169075·Eat Weight Disord·2008
8-other
Invoice choice. Children's Memorial Hospital finds the right antidote to speed up account payables.
PMID 17370887·Healthc Inform·2007
8-other
Correlation of patterns of denitrification instability in replicated bioreactor communities with shifts in the relative abundance and the denitrification patterns of specific populations.
PMID 18059495·ISME J·2007
8-other
Correlation of functional instability and community dynamics in denitrifying dispersed-growth reactors.
PMID 17142382·Appl Environ Microbiol·2007
8-other
The role of inhaled nitric oxide and heliox in the management of acute respiratory failure.
PMID 16952807·Respir Care Clin N Am·2006
6-review
Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.
PMID 15940687·Am J Med Genet A·2005
5-case
Medicolegal aspects of respiratory care and leadership responsibilities.
PMID 15177251·Respir Care Clin N Am·2004
6-review
Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication.
PMID 15108208·Am J Med Genet A·2004
5-case
Mechanisms of soluble beta-amyloid impairment of endothelial function.
PMID 15319431·J Biol Chem·2004
7-preclinical
FISH and cytogenetic characterization of a terminal chromosome 1q deletion: clinical case report and phenotypic implications.
PMID 12599188·Am J Med Genet A·2003
5-case
Targeting colon cancer cells with genistein-17.1A immunoconjugate.
PMID 12684659·Int J Oncol·2003
7-preclinical
Physiology and xanthophyll cycle activity of Nannochloropsis gaditana.
PMID 11536121·Biotechnol Bioeng·2001
8-other
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).
PMID 19574260·J Med Genet·2010
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 27699 JEFFERSON AVE, # 312
TEMECULA, CA 92590 - Phone
- (951) 676-4221
Quick Facts
- NPI
- 1861480998
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 34
- Publications
- 20
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