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

Yazar: Ronan, Shawn, Nusinowitz, Steve, Swaroop, Anand, Heckenlively, John R.
Baskı/Yayın Bilgisi 2006

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

Yazar: Spielberg, Leigh H, Heckenlively, John R, Leys, Anita M
Baskı/Yayın Bilgisi 2013

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

Yazar: Daiger, Stephen P., McGuire, Rachel E., Heckenlively, John R.
Baskı/Yayın Bilgisi 1996

Two mouse models for recoverin-associated autoimmune retinopathy

Yazar: Lu, Ying, He, Shirley, Jia, Lin, Khan, Naheed W., Heckenlively, John R.
Baskı/Yayın Bilgisi 2010

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

Yazar: Nikoopour, Enayat, Lin, Cheng-mao, Sheskey, Sarah, Heckenlively, John R., Lundy, Steven K.
Yayımlandı J Immunol (2019)

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

Yazar: Zahid, Sarwar, Peeler, Crandall, Khan, Naheed, Davis, Joy, Mahmood, Mahdi, Heckenlively, John, Jayasundera, Thiran
Yayımlandı 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

Yazar: Qian, Cynthia X., Branham, Kari, Khan, Naheed, Lundy, Steven K., Heckenlively, John R., Jayasundera, Thiran
Yayımlandı Ophthalmic Genet (2017)

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

Yazar: Daiger, Stephen P., Sullivan, Lori S., Gire, Anisa I., Birch, David G., Heckenlively, John R., Bowne, Sara J.
Baskı/Yayın Bilgisi 2008

Retinal Flavoprotein Autofluorescence as a Measure of Retinal Health

Yazar: Elner, Susan G., Elner, Victor M., Field, Matthew G., Park, Seung, Heckenlively, John R., Petty, Howard R.
Baskı/Yayın Bilgisi 2008

Melanoma-Associated Retinopathy: A Paraneoplastic Autoimmune Complication

Yazar: Lu, Ying, Jia, Lin, He, Shirley, Hurley, Mary C., Leys, Monique J., Jayasundera, Thiran, Heckenlively, John R.
Yayımlandı Arch Ophthalmol (2009)

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

Yazar: Abalem, Maria Fernanda, Musch, David C., Birch, David G., Pennesi, Mark E., Heckenlively, John R., Jayasundera, Thiran
Yayımlandı Ophthalmic Genet (2018)

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

Yazar: Otani, Atsushi, Dorrell, Michael Ian, Kinder, Karen, Moreno, Stacey K., Nusinowitz, Steven, Banin, Eyal, Heckenlively, John, Friedlander, Martin
Baskı/Yayın Bilgisi 2004

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

Yazar: Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Kennan, Avril, Humphries, Peter, Birch, David G., Heckenlively, John R.
Baskı/Yayın Bilgisi 2003

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

Yazar: Tzekov, Radouil T., Liu, Yuhui, Sohocki, Melanie M., Zack, Donald J., Daiger, Stephen P., Heckenlively, John R., Birch, David G.
Baskı/Yayın Bilgisi 2001

Detection of Retinal Metabolic Stress due to Central Serous Retinopathy

Yazar: Field, Matthew G., Elner, Victor M., Park, Seung, Hackel, Richard, Heckenlively, John R., Elner, Susan G., Petty, Howard R.
Baskı/Yayın Bilgisi 2009

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

Yazar: ZAHID, SARWAR, JAYASUNDERA, THIRAN, RHOADES, WILLIAM, BRANHAM, KARI, KHAN, NAHEED, NIZIOL, LESLIE M., MUSCH, DAVID C., HECKENLIVELY, JOHN R.
Yayımlandı Am J Ophthalmol (2012)

Double hyperautofluorescent ring on fundus autofluorescence in ABCA4

Yazar: Abalem, Maria Fernanda, Qian, Cynthia X., Branham, Kari, Schlegel, Dana, Fahim, Abigail T., Khan, Naheed W., Heckenlively, John, Jayasundera, Thiran
Yayımlandı Ophthalmic Genet (2017)

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

Yazar: Bowne, Sara J., Sullivan, Lori. S., Gire, Anisa I., Birch, David G., Hughbanks-Wheaton, Dianna, Heckenlively, John R., Daiger, Stephen P.
Baskı/Yayın Bilgisi 2008

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

Yazar: Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Birch, David G., Heckenlively, John R., Pierce, Eric A., Weinstock, George M.
Baskı/Yayın Bilgisi 2010

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

Yazar: Jayasundera, Thiran, Branham, Kari EH, Othman, Mohammad, Rhoades, William R, Karoukis, Athanasios J, Khanna, Hemant, Swaroop, Anand, Heckenlively, John R.
Baskı/Yayın Bilgisi 2010