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ANTONIO ROMAN, MD

MD

Psychiatry Physician

NPI: 1124009543Individual

Specialties, Licenses & Credentials

Psychiatry PhysicianPrimary

Psychiatry & Neurology — Psychiatry

Code: 2084P0800X

J7286(TX)

Research & Publications (20)

Maturation of O2 sensing and signaling in the chicken ductus arteriosus.
PMID 19617310·Am J Physiol Lung Cell Mol Physiol·2009
7-preclinical
Dioxin receptor deficiency impairs angiogenesis by a mechanism involving VEGF-A depletion in the endothelium and transforming growth factor-beta overexpression in the stroma.
PMID 19617630·J Biol Chem·2009
7-preclinical
Vision 1 year after gene therapy for Leber's congenital amaurosis.
PMID 19675341·N Engl J Med·2009
5-case
Sustained epidermal growth factor receptor levels and activation by tethered ligand binding enhances osteogenic differentiation of multi-potent marrow stromal cells.
PMID 19544388·J Cell Physiol·2009
8-other
New concepts in the invasive and non invasive evaluation of remodelling of the right ventricle and pulmonary vasculature in pulmonary arterial hypertension.
PMID 19452037·Open Respir Med J·2009
8-other
Improving epidemiological surveys of sexual behaviour conducted by telephone.
PMID 19448047·Int J Epidemiol·2009
2-rct
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year.
PMID 19583479·Hum Gene Ther·2009
3-trial
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
Response to paclitaxel in a radiotherapy-induced breast angiosarcoma.
PMID 19235566·Acta Oncol·2009
5-case
The dioxin receptor regulates the constitutive expression of the vav3 proto-oncogene and modulates cell shape and adhesion.
PMID 19158396·Mol Biol Cell·2009
7-preclinical
Copy number variation in the CCL4L gene is associated with susceptibility to acute rejection in lung transplantation.
PMID 19148142·Genes Immun·2009
8-other
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations.
PMID 19117922·Invest Ophthalmol Vis Sci·2009
8-other
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.
PMID 19074810·Invest Ophthalmol Vis Sci·2009
8-other
ABCA4 disease progression and a proposed strategy for gene therapy.
PMID 19074458·Hum Mol Genet·2009
8-other
Fetal fibronectin testing in patients with short cervix in the midtrimester: can it identify optimal candidates for ultrasound-indicated cerclage?
PMID 19070833·Am J Obstet Gynecol·2009
2-rct
Loss of dioxin-receptor expression accelerates wound healing in vivo by a mechanism involving TGFbeta.
PMID 19435800·J Cell Sci·2009
7-preclinical
Adipocyte differentiation of bone marrow-derived mesenchymal stem cells: cross talk with the osteoblastogenic program.
PMID 18854943·Cell Mol Life Sci·2009
6-review
A multicenter study of valganciclovir prophylaxis up to day 120 in CMV-seropositive lung transplant recipients.
PMID 19344437·Am J Transplant·2009
4-observational
Prolonged weakening of the geomagnetic field (GMF) affects the immune system of rats.
PMID 18563735·Bioelectromagnetics·2009
7-preclinical
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets.
PMID 18704120·Eye (Lond)·2009
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
6116 N CENTRAL EXPY, SUITE 915
DALLAS, TX 75206

Quick Facts

NPI
1124009543
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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