Professor of Ophthalmology, University Iowa College of Medicine
Ophthalmology
Dr. Wallace L. Alward, MD
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Wallace L. Alward practices Ophthalmology. He went to medical school at The Ohio State University College of Medicine. He received 3 awards: "America's Top Doctors", "CMS Meaningful Use Stage 1 Certification" and "Fellow (FAAO)". Dr. Wallace L. Alward is also published. He has 100 publications published. The lastest publication: "Medical management of glaucoma.' He accepts Medicare payments and is listed with Medicare.gov.
Publications
- Boston type 1 keratoprosthesis for primary congenital Glaucoma.
- IridoCorneal Endothelial Syndrome in a 14-Year-Old Male.
- Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly.
- A Vector Force Model of Upper Eyelid Position in the Setting of a Trabeculectomy Bleb.
- Movement of Retinal Vessels to Optic Nerve Head with IntraOcular Pressure Elevation in a Child.
- The Centennial of Modern Gonioscopy.
- Graft Survival Versus Glaucoma Treatment After Penetrating or Descemet Stripping Automated Endothelial Keratoplasty.
- Successful Long-term Management of Iris Flocculi and Miosis in a Patient With a Strong Family History of Thoracic Aortic Aneurysms and Dissections Associated With an M...
- Thin Central Corneal Thickness and Early-Onset Glaucoma in Lacrimo-auriculo-dento-digital Syndrome.
- Identification of Proteins that Interact with TANK Binding Kinase 1 and Testing for Mutations Associated with Glaucoma.
- Analysis of ASB10 variants in open angle Glaucoma.
- Circumferential Iris Transillumination Defects in Exfoliation Syndrome.
- Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle Glaucoma and steroid responders.
- Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil.
- Glaucoma therapy escalation in eyes with pseudophakic corneal Edema after penetrating keratoplasty and Descemet's stripping automated endothelial keratoplasty.
- Robust multiscale stereo matching from fundus images with radiometric differences.
- Copy number variations on chromosome 12q14 in patients with normal tension Glaucoma.
- Chromosome 7q31 POAG locus: Ocular expression of caveolins and lack of association with POAG in a US cohort.
- Copy number variations and primary open-angle Glaucoma.
- Genome-wide analysis of copy number variants in age-related Macular degeneration.
- A history of gonioscopy.
- Escalation of Glaucoma therapy after deep lamellar endothelial keratoplasty.
- A case-control comparison of the clinical characteristics of Glaucoma and ocular hypertensive patients with and without the myocilin Gln368Stop mutation.
- Rate and pattern of visual field decline in primary open-angle Glaucoma.
- Variations in the myocilin gene in patients with open-angle Glaucoma.
- Progressive axial myopia in a juvenile patient with traumatic Glaucoma.
- Automated segmentation of the cup and rim from spectral domain OCT of the optic nerve head.
- Variance owing to observer, repeat imaging, and fundus camera type on cup-to-disc ratio estimates by stereo planimetry.
- Primary open-angle Glaucoma.
- How I choose a prostaglandin analogue.
- Lyst mutation in mice recapitulates iris defects of human exfoliation Syndrome.
- LOXL1 mutations are associated with exfoliation Syndrome in patients from the midwestern United States.
- Heritable features of the optic disc: a novel twin method for determining genetic significance.
- Concordance of diurnal intraocular pressure between fellow Eyes in primary open-angle glaucoma.
- Diurnal fluctuation and concordance of intraocular pressure in Glaucoma suspects and normal tension Glaucoma patients.
- Automated segmentation of the optic disc from stereo color photographs using physiologically plausible features.
- Familial cavitary optic disk anomalies: identification of a novel genetic locus.
- Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cupping.
- No association between variations in the WDR36 gene and primary open-angle Glaucoma.
- Progressive iris changes in a case of Axenfeld-Rieger Syndrome.
- Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger Syndrome.
- The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation Glaucoma and primary open-angle glauco...
- Retinal synthesis and deposition of complement components induced by Ocular hypertension.
- Gonioscopy in primary angle closure Glaucoma.
- Macular degeneration and glaucoma-like optic nerve head cupping.
- Atypical Pigment dispersion syndrome in a child.
- Evaluation of optineurin sequence variations in 1,048 patients with open-angle Glaucoma.
- Rate of optic disc cup progression in treated primary open-angle Glaucoma.
- Biomedicine. A new angle on Ocular development.
- A family with Axenfeld-Rieger Syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.
- Myocilin Glaucoma.
- Screening for mutations of Axenfeld-Rieger Syndrome caused by FOXC1 gene in Japanese patients.
- Rate of visual field loss and long-term visual outcome in primary open-angle Glaucoma.
- Expression of the Glaucoma gene myocilin (MYOC) in the human optic nerve head.
- A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye.
- Long-term results of Eyes with penetrating keratoplasty and glaucoma drainage tube implant.
- Non-secretion of mutant proteins of the Glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humor.
- Evaluation of the myocilin (MYOC) Glaucoma gene in monkey and human steroid-induced ocular hypertension.
- Rieger Syndrome: a clinical, molecular, and biochemical analysis.
- The genetics of open-angle Glaucoma: the story of GLC1A and myocilin.
- Localization of MYOC transcripts in human eye and optic nerve by in situ hybridization.
- Axenfeld-Rieger Syndrome in the age of molecular genetics.
- Correlation of automated visual field parameters and peripapillary nerve fiber layer thickness as measured by scanning laser polarimetry.
- Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant Ocular development.
- Frequency doubling technology perimetry for the detection of Glaucomatous visual field loss.
- Combination of autologous blood injection and bleb compression sutures to treat Hypotony maculopathy.
- Myositis associated with a Baerveldt Glaucoma implant.
- Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects.
- Expression pattern and in situ localization of the mouse homologue of the human MYOC (GLC1A) gene in adult brain.
- Analysis of myocilin mutations in 1703 Glaucoma patients from five different populations.
- Control of intraOcular pressure after trabeculectomy.
- Medical management of Glaucoma.
- A novel homeobox gene PITX3 is mutated in families with autosomal-dominant Cataracts and ASMD.
- The forkhead transcription factor gene FKHL7 is responsible for Glaucoma phenotypes which map to 6p25.
- Characterization and comparison of the human and mouse GLC1A Glaucoma genes.
- Clinical features associated with mutations in the chromosome 1 open-angle Glaucoma gene (GLC1A)
- Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger Syndrome (RIEG/PITX2) gene.
- Unilateral pigment dispersion and Glaucoma caused by angle recession.
- Nonarteritic anterior ischemic optic neuropathy: role of nocturnal arterial hypotension.
- A randomized study of mitomycin augmentation in combined phacoemulsification and trabeculectomy.
- Identification of a gene that causes primary open angle Glaucoma.
- Incomplete elimination of exercise-induced Pigment dispersion by laser iridotomy in Pigment dispersion syndrome.
- Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger Syndrome.
- Fine mapping of the autosomal dominant juvenile open angle Glaucoma (GLC1A) region and evaluation of candidate genes.
- Molecular genetics of Glaucoma: current status.
- Genetic linkage of familial open angle Glaucoma to chromosome 1q21-q31.
- Clinical features and linkage analysis of a family with autosomal dominant juvenile Glaucoma.
- A placebo for mitomycin C.
- Experimental endoscopic goniotomy. A potential treatment for primary infantile Glaucoma.
- Asymmetric pigmentary Glaucoma caused by unilateral angle recession.
- Low-energy argon laser suture lysis after trabeculectomy.
- Nocturnal arterial hypotension and its role in optic nerve head and ocular ischemic Disorders.
- Aggressive nevus of the iris with secondary Glaucoma in a child.
- Combined phacoemulsification, posterior chamber intraocular Lens implantation, and trabeculectomy with mitomycin C.
- Linkage of posterior polymorphous Corneal dystrophy to 20q11.
- Tenon's cyst formation after trabeculectomy with mitomycin C.
- Linkage of autosomal dominant iris hypoplasia to the region of the Rieger Syndrome locus (4q25).
- Marked intraOcular pressure rise following blood injection into a filtering bleb.
- Pigment dispersion secondary to cysts of the iris Pigment epithelium.
Schools
Ohio State University College of Medicine
University Hosps
University Of Louisville
Bascom Palmer University Miami
Procedures Preformed
- Anterior Vitrectomy
- Cataract Removal Surgery
- Cornea Transplant
- Destruction of Lesion of Retina and Choroid
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Conditions Treated
- Acute Endophthalmitis
- Age-Related Macular Degeneration
- Aphakia and Other Disorders of Lens
- Astigmatism
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Doctors Specialties
- Ophthalmology
Accepted Insurances
Awards
- America's Top Doctors
- CMS Meaningful Use Stage 1 Certification
- Fellow (FAAO)
Education
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Jackson Memorial Hospital - Jackson Health System -
University of Louisville -
University of Pittsburgh Medical Center -
The Ohio State University College of Medicine
Drug Facts
| NPI NUMBER | 1063413417 | |
| NPPES Provider LastName | ALWARD | |
| NPPES Provider FirstName | WALLACE | |
| NPPES Provider ZIPCode | 522421009 | |
| NPPES Provider State | IA | |
| Specialty Description | Ophthalmology | |
| Total Claim Count | 1808.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1063413417 |
| Last Name Of The Provider | ALWARD |
| First Name Of The Provider | WALLACE |
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