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

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)

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)

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

Ablation of the X-Linked Retinitis Pigmentosa 2 (Rp2) Gene in Mice Results in Opsin Mislocalization and Photoreceptor Degeneration

Por Li, Linjing, Khan, Naheed, Hurd, Toby, Ghosh, Amiya Kumar, Cheng, Christiana, Molday, Robert, Heckenlively, John R., Swaroop, Anand, Khanna, Hemant
Publicado em 2013

Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies

Por Chaki, Moumita, Hoefele, Julia, Allen, Susan J., Ramaswami, Gokul, Janssen, Sabine, Bergmann, Carsten, Heckenlively, John R., Otto, Edgar A., Hildebrandt, Friedhelm
Publicado em 2011

The Need for Standardization of Antiretinal Antibody Detection and Measurement

Por Forooghian, Farzin, MacDonald, Ian M., Heckenlively, John R., Héon, Elise, Gordon, Lynn K., Hooks, John J., Detrick, Barbara, Nussenblatt, Robert B.
Publicado em 2008

XIAP Therapy Increases Survival of Transplanted Rod Precursors in a Degenerating Host Retina

Por Yao, Jingyu, Feathers, Kecia L., Khanna, Hemant, Thompson, Debra, Tsilfidis, Catherine, Hauswirth, William W., Heckenlively, John R., Swaroop, Anand, Zacks, David N.
Publicado em 2011

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice

Por Anderson, Michael G, Smith, Richard S, Savinova, Olga V, Hawes, Norman L, Chang, Bo, Zabaleta, Adriana, Wilpan, Robert, Heckenlively, John R, Davisson, Muriel, John, Simon WM
Publicado em 2001

Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa

Por Bowne, Sara J., Sullivan, Lori S., Blanton, Susan H., Cepko, Constance L., Blackshaw, Seth, Birch, David G., Hughbanks-Wheaton, Dianna, Heckenlively, John R., Daiger, Stephen P.
Publicado em 2002