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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
Intrinsic toxicity of hemoglobin: how to counteract it.
PMID 19178453·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

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

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Contact & Hours

Address
555 MARIN ST STE 270
THOUSAND OAKS, CA 91360

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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