Research Associate in Ophthalmology, Schepens Eye Research Institute
Ophthalmology
Dr. Shahrokh C. Khani, MD
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Shahrokh Khani practices Ophthalmology. He researched medicine at Medical College of Wisconsin Affiliated Hospitals. He received awards:"Fellow (FAAO)". Shahrokh C. Khani is a published doctor as well. He has 21 publications published. The latest was: Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the oguchi form of congenital stationary night blindness. He is registered with Medicare and accepts Medicare payments.
Publications
- Regulation of mammalian cone phototransduction by recoverin and rhodopsin kinase.
- Variation in rhodopsin kinase expression alters the dim flash response shut off and the light adaptation in rod photoreceptors.
- Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis.
- Effect of g protein-coupled receptor kinase 1 (Grk1) overexpression on rod photoreceptor cell viability.
- Expression characteristics of dual-promoter lentiviral vectors targeting Retinal photoreceptors and Müller cells.
- AAV-mediated expression targeting of rod and cone photoreceptors with a human rhodopsin kinase promoter.
- Conserved interactions of a compact highly active enhancer/promoter upstream of the rhodopsin kinase (GRK1) gene.
- Conserved structure and spatiotemporal function of the compact rhodopsin kinase (GRK1) enhancer/promoter.
- A short, highly active photoreceptor-specific enhancer/promoter region upstream of the human rhodopsin kinase gene.
- Late-onset autosomal dominant macular dystrophy with Choroidal neovascularization and nonexudative maculopathy associated with mutation in the RDS gene.
- Isolation and partial characterization of the gene for cytochrome P-450 3a (P-450ALC) and a second closely related gene.
- Posterior segment intraocular foreign bodies.
- Gene therapy with a promoter targeting both rods and cones rescues Retinal degeneration caused by AIPL1 mutations.
- Molecular forms of human rhodopsin kinase (GRK1).
- Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man.
- 11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.
- Characterization and chromosomal localization of the gene for human rhodopsin kinase.
- Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosa.
- Biochemical evidence for pathogenicity of rhodopsin kinase mutations correlated with the oguchi form of congenital stationary night blindness.
- Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.
Schools
University of Mi Med Sch
St Joseph Mercy Hospital
Washington University School Med
Mass Eye and Ear
Med College Wis
Procedures Preformed
- Cataract Removal Surgery
- Destruction of Lesion of Retina and Choroid
- Paracentesis of Anterior Eye
- Repair of Retinal Detachment or Retinal Tear
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Conditions Treated
- Benign Neoplasm of Choroid
- Benign Neoplasm of Eye
- Blepharitis
- Cataract
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Doctors Specialties
- Ophthalmology
Accepted Insurances
Awards
- Fellow (FAAO)
Education
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Medical College of Wisconsin Affiliated Hospitals -
Washington University - Barnes-Jewish Hospital -
St Joseph Mercy Livingston Hospital -
University of Michigan Medical School
Hospital
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UMass Memorial Medical Center -
Beverly Hospital
Drug Facts
| NPI NUMBER | 1710953690 | |
| NPPES Provider LastName | KHANI | |
| NPPES Provider FirstName | SHAHROKH | |
| NPPES Provider ZIPCode | 019156181 | |
| NPPES Provider State | MA | |
| Specialty Description | Ophthalmology | |
| Total Claim Count | 192.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1710953690 |
| Last Name Of The Provider | KHANI |
| First Name Of The Provider | SHAHROKH |
| View All |
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