Finding and interpreting genetic variations that are important to ophthalmologists.

Por Stone, Edwin M
Publicado em 2003

Progress Toward Effective Treatments for Human Photoreceptor Degenerations

Por Stone, Edwin M.
Publicado no Curr Opin Genet Dev (2009)

Patients with an Acute Zonal Occult Outer Retinopathy-like Illness Rapidly Improve with Valacyclovir Treatment

Por Mahajan, Vinit B., Stone, Edwin M.
Publicado no Am J Ophthalmol (2010)

Which Leber congenital amaurosis patients are eligible for gene therapy trials?

Por Drack, Arlene V., Johnston, Rebecca, Stone, Edwin M.
Publicado em 2009

From the Laboratory to the Clinic: Molecular Genetic Testing in Pediatric Ophthalmology

Por Drack, Arlene V., Lambert, Scott R., Stone, Edwin M.
Publicado em 2010

Stem cells for investigation and treatment of inherited retinal disease

Por Tucker, Budd A., Mullins, Robert F., Stone, Edwin M.
Publicado em 2014

Autologous cell replacement: a noninvasive AI approach to clinical release testing

Por Tucker, Budd A., Mullins, Robert F., Stone, Edwin M.
Publicado no J Clin Invest (2020)

Peripapillary Retinal Nerve Fiber Layer Thinning in Patients With Autosomal Recessive Cone-Rod Dystrophy

Por PASADHIKA, SIRICHAI, FISHMAN, GERALD A., ALLIKMETS, RANDO, STONE, EDWIN M.
Publicado em 2009

Treatment of Adult-Onset Acute Macular Retinoschisis in Enhanced-S Cone Syndrome with Oral Acetazolamide

Por Iannaccone, Alessandro, Fung, Kenneth H., Eyestone, Mari E., Stone, Edwin M.
Publicado em 2008

Fibulin-5 Distribution in Human Eyes: Relevance to Age-Related Macular Degeneration

Por Mullins, Robert F., Olvera, Marissa A., Clark, Abbot F., Stone, Edwin M.
Publicado em 2006

BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes

Por Zhang, Qihong, Seo, Seongjin, Bugge, Kevin, Stone, Edwin M., Sheffield, Val C.
Publicado em 2012

Intrinsic Protein-Protein Interaction-mediated and Chaperonin-assisted Sequential Assembly of Stable Bardet-Biedl Syndrome Protein Complex, the BBSome

Por Zhang, Qihong, Yu, Dahai, Seo, Seongjin, Stone, Edwin M., Sheffield, Val C.
Publicado em 2012

Selective Accumulation of the Complement Membrane Attack Complex in Aging Choriocapillaris

Por Chirco, Kathleen R., Tucker, Budd A., Stone, Edwin M., Mullins, Robert F.
Publicado no Exp Eye Res (2015)

Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by light

Por Thompson, Stewart, Foster, Russell G., Stone, Edwin M., Sheffield, Val C., Mrosovsky, N.
Publicado em 2008

Computational Quantification of Complex Fundus Phenotypes in Age-Related Macular Degeneration and Stargardt Disease

Por Quellec, Gwenole, Russell, Stephen R., Scheetz, Todd E., Stone, Edwin M., Abràmoff, Michael D.
Publicado em 2011

Fluocinolone Acetonide Implant Inhibits Neovascularization but not Fibrosis in Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy

Por Tlucek, Paul S., Folk, James C., Orien, Jason A., Stone, Edwin M., Mahajan, Vinit B.
Publicado em 2012

THE VALUE OF RETINAL IMAGING WITH INFRARED SCANNING LASER OPHTHALMOSCOPY IN PATIENTS WITH STARGARDT DISEASE

Por Chun, Robert, Fishman, Gerald A., Collison, Frederick T., Stone, Edwin M., Zernant, Jana, Allikmets, Rando
Publicado em 2014

Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis

Por Drivas, Theodore G., Wojno, Adam P., Tucker, Budd A., Stone, Edwin M., Bennett, Jean
Publicado no Sci Transl Med (2015)

Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front

Por Cideciyan, Artur V., Swider, Malgorzata, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.
Publicado no Invest Ophthalmol Vis Sci (2015)

Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India

Por Sundaresan, Periasamy, Vijayalakshmi, P., Thompson, Stewart, Ko, Audrey C., Fingert, John H., Stone, Edwin M.
Publicado em 2009