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GILBERT SIMONI, M.D., FACG
M.D., FACG
Gastroenterology Physician
NPI: 1316922958Individual
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
A77140(CA)
Gastroenterology PhysicianPrimary
Internal Medicine — Gastroenterology
Code: 207RG0100X
MA74330(NJ)A77140(CA)
Hepatology Physician
Internal Medicine — Hepatology
Code: 207RI0008X
A77140(CA)
CMS Specialties
PrimaryGASTROENTEROLOGY
Education
OTHER
Class of 1999
Research & Publications (20)
Control of oxidative reactions of hemoglobin in the design of blood substitutes: role of the ascorbate-glutathione antioxidant system.
PMID 19178455·Artif Organs·2009
7-preclinical
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1).
PMID 19353688·Am J Med Genet A·2009
5-case
Eosinophilic cholecystitis, with a review of the literature.
PMID 17522376·Ann Clin Lab Sci·2007
5-case
Evaluation of angiotensin converting enzyme (ACE)-like activity of acellular hemoglobin.
PMID 17453704·Artif Cells Blood Substit Immobil Biotechnol·2007
8-other
Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndrome.
PMID 17259293·J Med Genet·2007
5-case
Detection of human immunodeficiency virus-1 RNA and DNA by extractive and in situ PCR in unprocessed semen and seminal fractions isolated by semen-washing procedure.
PMID 16476677·Hum Reprod·2006
8-other
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi.
PMID 16418738·Eur J Hum Genet·2006
8-other
X chromosome monosomy: a common mechanism for autoimmune diseases.
PMID 15972694·J Immunol·2005
8-other
Three cases with de novo 6q imbalance and variable prenatal phenotype.
PMID 15957159·Am J Med Genet A·2005
5-case
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells.
PMID 15781624·Cancer Res·2005
8-other
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies.
PMID 15664406·Placenta·2005
4-observational
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.
PMID 14673477·Eur J Hum Genet·2004
8-other
Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.
PMID 15614836·Prenat Diagn·2004
8-other
Endovascular abdominal aortic aneurysm repair in patients with challenging anatomy: utility of the hybrid endograft.
PMID 15248640·Vascular·2004
4-observational
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes.
PMID 15005689·J Cutan Pathol·2004
8-other
Frequency of monosomy X in women with primary biliary cirrhosis.
PMID 14975617·Lancet·2004
4-observational
Genetic characterization of the three medicinal Echinacea species using RAPD analysis.
PMID 12898432·Planta Med·2003
8-other
Regarding "Carotid artery closure for endarterectomy does not influence results of angioplasty-stenting for restenosis".
PMID 12514615·J Vasc Surg·2003
8-other
Presence of fetal DNA in maternal plasma decades after pregnancy.
PMID 12107445·Hum Genet·2002
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
- 555 MARIN ST STE 270
THOUSAND OAKS, CA 91360 - Phone
- (805) 719-0244
Quick Facts
- NPI
- 1316922958
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 1
- Years in Practice
- 27
- Publications
- 20
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