SENILE PANRETINAL CONE DYSFUNCTION IN AGE-RELATED MACULAR DEGENERATION (AMD): A REPORT OF 52 AMD PATIENTS COMPARED TO AGE-MATCHED CONTROLS

Por Ronan, Shawn, Nusinowitz, Steve, Swaroop, Anand, Heckenlively, John R.
Publicado em 2006

Retinal pigment epithelial detachments and tears, and progressive retinal degeneration in light chain deposition disease

Por Spielberg, Leigh H, Heckenlively, John R, Leys, Anita M
Publicado em 2013

Reply to Inglehearn and Hardcastle: The Map Is Not the Territory

Por Daiger, Stephen P., McGuire, Rachel E., Heckenlively, John R.
Publicado em 1996

Two mouse models for recoverin-associated autoimmune retinopathy

Por Lu, Ying, He, Shirley, Jia, Lin, Khan, Naheed W., Heckenlively, John R.
Publicado em 2010

Immune Cell Infiltration into the Eye is Controlled by Interleukin 10 in Recoverin-Induced Autoimmune Retinopathy

Por Nikoopour, Enayat, Lin, Cheng-mao, Sheskey, Sarah, Heckenlively, John R., Lundy, Steven K.
Publicado no J Immunol (2019)

Digital Quantification of Goldmann Visual Fields (GVF) as a Means for Genotype-Phenotype Comparisons and Detection of Progression in Retinal Degenerations

Por Zahid, Sarwar, Peeler, Crandall, Khan, Naheed, Davis, Joy, Mahmood, Mahdi, Heckenlively, John, Jayasundera, Thiran
Publicado no Adv Exp Med Biol (2014)

Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy

Por Qian, Cynthia X., Branham, Kari, Khan, Naheed, Lundy, Steven K., Heckenlively, John R., Jayasundera, Thiran
Publicado no Ophthalmic Genet (2017)

MUTATIONS IN KNOWN GENES ACCOUNT FOR 58% OF AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA (adRP)

Por Daiger, Stephen P., Sullivan, Lori S., Gire, Anisa I., Birch, David G., Heckenlively, John R., Bowne, Sara J.
Publicado em 2008

Retinal Flavoprotein Autofluorescence as a Measure of Retinal Health

Por Elner, Susan G., Elner, Victor M., Field, Matthew G., Park, Seung, Heckenlively, John R., Petty, Howard R.
Publicado em 2008

Melanoma-Associated Retinopathy: A Paraneoplastic Autoimmune Complication

Por Lu, Ying, Jia, Lin, He, Shirley, Hurley, Mary C., Leys, Monique J., Jayasundera, Thiran, Heckenlively, John R.
Publicado no Arch Ophthalmol (2009)

Diurnal variations of foveoschisis by optical coherence tomography in patients with RS1 X-linked retinoschisis

Por Abalem, Maria Fernanda, Musch, David C., Birch, David G., Pennesi, Mark E., Heckenlively, John R., Jayasundera, Thiran
Publicado no Ophthalmic Genet (2018)

Rescue of retinal degeneration by intravitreally injected adult bone marrow–derived lineage-negative hematopoietic stem cells

Por Otani, Atsushi, Dorrell, Michael Ian, Kinder, Karen, Moreno, Stacey K., Nusinowitz, Steven, Banin, Eyal, Heckenlively, John, Friedlander, Martin
Publicado em 2004

IDENTIFICATION OF THE RP1 AND RP10 (IMPDH1) GENES CAUSING AUTOSOMAL DOMINANT RP

Por Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Kennan, Avril, Humphries, Peter, Birch, David G., Heckenlively, John R.
Publicado em 2003

Autosomal Dominant Retinal Degeneration and Bone Loss in Patients with a 12-bp Deletion in the CRX Gene

Por Tzekov, Radouil T., Liu, Yuhui, Sohocki, Melanie M., Zack, Donald J., Daiger, Stephen P., Heckenlively, John R., Birch, David G.
Publicado em 2001

Detection of Retinal Metabolic Stress due to Central Serous Retinopathy

Por Field, Matthew G., Elner, Victor M., Park, Seung, Hackel, Richard, Heckenlively, John R., Elner, Susan G., Petty, Howard R.
Publicado em 2009

Clinical Phenotypes and Prognostic Full-Field Electroretinographic Findings in Stargardt Disease

Por ZAHID, SARWAR, JAYASUNDERA, THIRAN, RHOADES, WILLIAM, BRANHAM, KARI, KHAN, NAHEED, NIZIOL, LESLIE M., MUSCH, DAVID C., HECKENLIVELY, JOHN R.
Publicado no Am J Ophthalmol (2012)

Double hyperautofluorescent ring on fundus autofluorescence in ABCA4

Por Abalem, Maria Fernanda, Qian, Cynthia X., Branham, Kari, Schlegel, Dana, Fahim, Abigail T., Khan, Naheed W., Heckenlively, John, Jayasundera, Thiran
Publicado no Ophthalmic Genet (2017)

Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa

Por Bowne, Sara J., Sullivan, Lori. S., Gire, Anisa I., Birch, David G., Hughbanks-Wheaton, Dianna, Heckenlively, John R., Daiger, Stephen P.
Publicado em 2008

Targeted High-Throughput DNA Sequencing for Gene Discovery in Retinitis Pigmentosa

Por Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Birch, David G., Heckenlively, John R., Pierce, Eric A., Weinstock, George M.
Publicado em 2010

THE RP2 PHENOTYPE AND PATHOGENETIC CORRELATIONS IN X-LINKED RETINITIS PIGMENTOSA

Por Jayasundera, Thiran, Branham, Kari EH, Othman, Mohammad, Rhoades, William R, Karoukis, Athanasios J, Khanna, Hemant, Swaroop, Anand, Heckenlively, John R.
Publicado em 2010