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CRISTINA SOLIS, MD
MD
Family Medicine Physician
NPI: 1497827216IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
G77916(CA)37108(OK)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UN OF CALIFORNIA, IRVINE, COLLEGE OF MEDICINE
Class of 1992
Research & Publications (12)
Preschoolers, parents, and teachers (PPT): a preventive intervention with an at risk population.
PMID 19441968·Int J Group Psychother·2009
2-rct
Retroperitoneal mesenteric duplication cysts with malignant transformation in adulthood.
PMID 19350866·Am Surg·2009
5-case
Choline intake, plasma riboflavin, and the phosphatidylethanolamine N-methyltransferase G5465A genotype predict plasma homocysteine in folate-deplete Mexican-American men with the methylenetetrahydrofolate reductase 677TT genotype.
PMID 19211833·J Nutr·2009
8-other
Adequate Intake levels of choline are sufficient for preventing elevations in serum markers of liver dysfunction in Mexican American men but are not optimal for minimizing plasma total homocysteine increases after a methionine load.
PMID 18779284·Am J Clin Nutr·2008
8-other
Silencing genes by RNA interference in the protozoan parasite Entamoeba histolytica.
PMID 18369782·Methods Mol Biol·2008
7-preclinical
Folate intake at RDA levels is inadequate for Mexican American men with the methylenetetrahydrofolate reductase 677TT genotype.
PMID 18156406·J Nutr·2008
2-rct
Acute intermittent porphyria: studies of the severe homozygous dominant disease provides insights into the neurologic attacks in acute porphyrias.
PMID 15534187·Arch Neurol·2004
5-case
Purification and molecular cloning of and immunization with Ancylostoma ceylanicum excretory-secretory protein 2, an immunoreactive protein produced by adult hookworms.
PMID 15039344·Infect Immun·2004
7-preclinical
Analysis of colored teeth from Precolumbian Tlatelolco: postmortem transformation or intravitam processes?
PMID 12489138·Am J Phys Anthropol·2003
8-other
Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria.
PMID 11254675·J Clin Invest·2001
8-other
Human uroporphyrinogen-III synthase: genomic organization, alternative promoters, and erythroid-specific expression.
PMID 11112350·Genomics·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
- 18503 N PORTLAND AVE
EDMOND, OK 73012 - Phone
- (405) 531-4271
Quick Facts
- NPI
- 1497827216
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 34
- Publications
- 12
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