Back to Search

AUGUSTO OCHOA, MD

MD

Pediatric Allergy/Immunology Physician

NPI: 1386665305Individual

Specialties, Licenses & Credentials

Pediatric Allergy/Immunology PhysicianPrimary

Pediatrics — Pediatric Allergy/Immunology

Code: 2080P0201X

025411(LA)

Research & Publications (20)

Arginase, prostaglandins, and myeloid-derived suppressor cells in renal cell carcinoma.
PMID 17255300·Clin Cancer Res·2007
6-review
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
PMID 18823326·Epilepsia·2009
8-other
Tumor-infiltrating regulatory dendritic cells inhibit CD8+ T cell function via L-arginine metabolism.
PMID 19293186·Cancer Res·2009
7-preclinical
T cell CD3 receptor zeta (TCRzeta)-chain expression in children with idiopathic nephrotic syndrome.
PMID 19082633·Pediatr Nephrol·2009
8-other
Arginase I-producing myeloid-derived suppressor cells in renal cell carcinoma are a subpopulation of activated granulocytes.
PMID 19201693·Cancer Res·2009
7-preclinical
Clinical and genetic characteristics of Mexican Huntington's disease patients.
PMID 19672992·Mov Disord·2009
8-other
Health indicators in the European regions: expanding regional comparisons to the new countries of the European Union - ISARE III.
PMID 19615705·Public Health·2009
8-other
Cytokine genetic polymorphisms and prostate cancer aggressiveness.
PMID 19474090·Carcinogenesis·2009
8-other
Arginine regulation by myeloid derived suppressor cells and tolerance in cancer: mechanisms and therapeutic perspectives.
PMID 18364002·Immunol Rev·2008
6-review
Interactions of cytokine gene polymorphisms in prostate cancer risk.
PMID 18174250·Carcinogenesis·2008
8-other
Effects of raloxifene therapy on circulating osteoprotegerin and RANK ligand levels in post-menopausal osteoporosis.
PMID 18560259·J Endocrinol Invest·2008
3-trial
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy.
PMID 18505993·Neurology·2008
8-other
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.
PMID 18514161·Am J Hum Genet·2008
8-other
Health indicators in the European regions--ISARE II.
PMID 17766265·Eur J Public Health·2008
8-other
Ethnic differences in cytokine gene polymorphisms: potential implications for cancer development.
PMID 17618436·Cancer Immunol Immunother·2008
8-other
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
PMID 17427938·Mov Disord·2007
8-other
Amodiaquine failure associated with erythrocytic glutathione in Plasmodium falciparum malaria.
PMID 17451604·Malar J·2007
7-preclinical
Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
PMID 17474109·Ann Neurol·2007
8-other
Computing van der Waals energies in the context of the rotamer approximation.
PMID 17554777·Proteins·2007
8-other
A randomized trial comparing the efficacy and tolerability of two HAART strategies at two years in antiretroviral naive patients.
PMID 17915162·Rev Clin Esp·2007
4-observational

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

Contact & Hours

Address
200 HENRY CLAY AVE
NEW ORLEANS, LA 70118

Location

Practice Location

200 HENRY CLAY AVE, NEW ORLEANS, LA
(504) 412-1835

Quick Facts

NPI
1386665305
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

Are you this provider?

Claim Your Profile