Associate Professor, Ophthalmology, University of Tennessee Health Science Center College of Medicine
Ophthalmology
Dr. Alessandro Iannaccone, MD
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Dr. Alessandro Iannaccone is an expert in the field of Ophthalmology. Alessandro Iannaccone is a published doctor and has 71 publications published. The lastest was: 'Plasma endothelin-1 concentrations in patients with retinal vein occlusions.' Alessandro Iannaccone, MD accepts Medicare payments and is registered with Medicare.gov.
Publications
- Abnormal cone ERGs in a family with congenital nystagmus and photophobia harboring a p.X423Lfs mutation in the PAX6 gene.
- Advancing therapeutic strategies for inherited retinal Degeneration: recommendations from the Monaciano Symposium.
- Author response: additional considerations in the utility of dark adaptometry for the diagnosis of age-related Macular degeneration.
- Macular pigment optical density is related to cognitive function in older people.
- Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and Juvenile retinitis pigmentosa patients by targeted next generation sequencing.
- Randomized Trial of Ciliary Neurotrophic Factor Delivered by Encapsulated Cell Intraocular Implants for Retinitis Pigmentosa.
- Methods and Reproducibility of Grading Optimized Digital Color Fundus Photographs in the Age-Related Eye Disease Study 2 (AREDS2)(AREDS2 Report Number 2).
- Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene.
- Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease.
- Bilateral paraneoplastic Optic neuropathy and unilateral retinal compromise in association with prostate cancer: a differential diagnostic challenge in a patient with ...
- Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
- Contribution of Muller cells toward the regulation of photoreceptor outer segment assembly.
- Predicting the pathogenicity of RPE65 mutations.
- Clinical and immunohistochemical evidence for an X linked Retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation.
- Functionally rodless mice: transgenic models for the investigation of cone function in Retinal disease and therapy.
- Genotype-phenotype correlations and differential diagnosis in autosomal dominant Macular disease.
- Pigment epithelium-derived factor supports normal Muller cell development and glutamine synthetase expression after removal of the Retinal pigment epithelium.
- Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.
- Reliability assessment of a rod photoreceptor outer segment grading system.
- Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).
- Lactose supports Muller cell protein expression patterns in the absence of the Retinal pigment epithelium.
- Targeted disruption of Muller cell metabolism induces photoreceptor dysmorphogenesis.
- Pigment epithelium-derived factor supports normal development of photoreceptor neurons and opsin expression after Retinal pigment epithelium removal.
- Disease expression of RP1 mutations causing autosomal dominant Retinitis pigmentosa.
- Effect of isosorbide mononitrate on the human optic nerve and Choroidal circulations.
- Clinical and functional features of patients with dominant Optic atrophy.
- Plasma endothelin-1 concentrations in patients with Retinal vein occlusions.
- Circulating endothelin-1 in non-insulin-dependent diabetic patients with retinopathy.
- The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic Retinitis pigmentosa.
- Autosomal-dominant Retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observations.
- Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotype.
- Correlation between Goldmann perimetry and maximal electroretinogram response in Retinitis pigmentosa.
- Low-noise electroretinogram recording techniques in Retinitis pigmentosa.
- Clinical heterogeneity of dominant Optic atrophy: the contribution of visual function investigations to diagnosis.
- Autosomal dominant simple microphthalmos.
- Electrophysiologic monitoring of diabetic retinopathy in pregnancy.
- Human Retinal hemodynamics following administration of 5-isosorbide mononitrate.
- Localization and distribution of wolframin in human tissues.
- Autoimmune biomarkers in age-related Macular degeneration: a possible role player in disease development and progression.
- Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations: Safety and Efficacy in 15 Children and Adults Followed Up to 3 Years.
- Diversity in autoimmunity against Retinal, neuronal, and axonal antigens in acquired neuro-retinopathy.
- Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related Macular degeneration.
- The association of Cataract with leukocyte telomere length in older adults: defining a new marker of aging.
- Autosomal recessive best vitelliform Macular dystrophy: report of a family and management of early-onset neovascular complications.
- Treatment of adult-onset acute Macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide.
- Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome.
- Contribution of Müller cells toward the regulation of photoreceptor outer segment assembly.
- Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.
- Identification of two novel mutations in families with X-linked ocular albinism.
- Clinical and functional findings in Choroideremia due to complete deletion of the CHM gene.
- Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.
- Macular pigment optical density in the elderly: findings in a large biracial Midsouth population sample.
- Estimation of Macular pigment optical density in the elderly: test-retest variability and effect of optical blur in pseudophakic subjects.
- Age-related decline in VIP-positive parasympathetic nerve fibers in the human submacular Choroid.
- Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects.
- Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor Degeneration.
- An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation.
- Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 gene.
- Correlates of serum lutein + zeaxanthin: findings from the Third National Health and Nutrition Examination Survey.
- Usher syndrome: correlation between Visual field size and maximal ERG response b-wave amplitude.
- Increasing evidence for syndromic phenotypes associated with RPGR mutations.
- Kinetics of Visual field loss in Usher syndrome Type II.
- Permissive glycan support of photoreceptor outer segment assembly occurs via a non-metabolic mechanism.
- Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
- Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
- Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations.
- Familial unilateral Brown syndrome.
- Visual evoked potentials in children with neurofibromatosis type 1.
- A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked Retinitis pigmentosa.
- Downregulation of a unique photoreceptor protein correlates with improper outer segment assembly.
Schools
University Of Tennessee Health Science Center College Of Medicine
Conditions Treated
- Aphakia and Other Disorders of Lens
- Benign Neoplasm of Choroid
- Benign Neoplasm of Eye
- Blindness
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Doctors Specialties
- Ophthalmology
Accepted Insurances
Education
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Sapienza University of Rome
Hospital
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University of Tennessee Medical Center
Drug Facts
| NPI NUMBER | 1306802434 | |
| NPPES Provider LastName | IANNACCONE | |
| NPPES Provider FirstName | ALESSANDRO | |
| NPPES Provider ZIPCode | 381322113 | |
| NPPES Provider State | TN | |
| Specialty Description | Ophthalmology | |
| Total Claim Count | 81.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1306802434 |
| Last Name Of The Provider | IANNACCONE |
| First Name Of The Provider | ALESSANDRO |
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