Cideciyan, Artur V.: search on Z-Library

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1

Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy

Artur V. Cideciyan

Journal:

Progress in Retinal and Eye Research

Year:

2010

Language:

english

File:

PDF, 2.86 MB

english, 2010

2

A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews

Lina Zelinger, Eyal Banin, Alexey Obolensky, Liliana Mizrahi-Meissonnier, Avigail Beryozkin, Dikla Bandah-Rozenfeld, Shahar Frenkel, Tamar Ben-Yosef, Saul Merin, Sharon B. Schwartz, Artur V. Cideciyan

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 1.30 MB

english, 2011

3

Foveal Therapy in Blue Cone Monochromacy: Predictions of Visual Potential From Artificial Intelligence

Sumaroka, Alexander, Cideciyan, Artur V., Sheplock, Rebecca, Wu, Vivian, Kohl, Susanne, Wissinger, Bernd, Jacobson, Samuel G.

Journal:

Frontiers in Neuroscience

Year:

2020

File:

PDF, 8.18 MB

2020

4

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

Haider, Neena B., Jacobson, Samuel G., Cideciyan, Artur V., Swiderski, Ruth, Streb, Luan M., Searby, Charles, Beck, Gretel, Hockey, Robin, Hanna, David B., Gorman, Susan

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 974 KB

english, 2000

5

Safety in Nonhuman Primates of Ocular AAV2-RPE65, a Candidate Treatment for Blindness in Leber Congenital Amaurosis

Jacobson, Samuel G., Boye, Sanford L., Aleman, Tomas S., Conlon, Thomas J., Zeiss, Caroline J., Roman, Alejandro J., Cideciyan, Artur V., Schwartz, Sharon B., Komaromy, Andras M., Doobrajh, Michelle

Journal:

Human Gene Therapy

Year:

2006

Language:

english

File:

PDF, 546 KB

english, 2006

6

Sites of disease action in a retinal dystrophy with supernormal and delayed rod electroretinogramb-waves

Donald C. Hood, Artur V. Cideciyan, Daniel A. Halevy, Samuel G. Jacobson

Journal:

Vision Research

Year:

1996

Language:

english

File:

PDF, 1.32 MB

english, 1996

7

Drusen and Photoreceptor Abnormalities in African-Americans with Intermediate Non-neovascular Age-related Macular Degeneration

Sadigh, Sam, Luo, Xunda, Cideciyan, Artur V., Sumaroka, Alexander, Boxley, Stacy L., Hall, Laura M., Sheplock, Rebecca, Feuer, William J., Stambolian, Dwight S., Jacobson, Samuel G.

Journal:

Current Eye Research

Year:

2015

Language:

english

File:

PDF, 532 KB

english, 2015

8

Autofluorescence Imaging With Near-Infrared Excitation: Normalization by Reflectance to Reduce Signal From Choroidal Fluorophores

Cideciyan, Artur V., Swider, Malgorzata, Jacobson, Samuel G.

Journal:

Investigative Opthalmology & Visual Science

Year:

2015

Language:

english

File:

PDF, 2.02 MB

english, 2015

9

881. Safety, Efficacy and Biodistribution of Recombinant AAV2-RPE65 Vector Delivered by Ocular Subretinal Injection

Jacobson, Samuel G., Acland, Gregory M., Aguirre, Gustavo D., Aleman, Tomas S., Boye, Sanford L., Schwartz, Sharon B., Cideciyan, Artur V., Zeiss, Caroline J., Komaromy, Andras M., Roman, Alejandro J.

Journal:

Molecular Therapy

Year:

2006

Language:

english

File:

PDF, 82 KB

english, 2006

10

Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease

Schönbach, Etienne M., Ibrahim, Mohamed A., Strauss, Rupert W., Birch, David G., Cideciyan, Artur V., Hahn, Gesa Astrid, Ho, Alexander, Kong, Xiangrong, Nasser, Fadi, Sunness, Janet S., Zrenner, Eberh

Journal:

Ophthalmology Retina

Year:

2017

Language:

english

File:

PDF, 1.23 MB

english, 2017

11

Improvement and Decline in Vision with Gene Therapy in Childhood Blindness

Jacobson, Samuel G., Cideciyan, Artur V., Roman, Alejandro J., Sumaroka, Alexander, Schwartz, Sharon B., Heon, Elise, Hauswirth, William W.

Journal:

New England Journal of Medicine

Year:

2015

Language:

english

File:

PDF, 556 KB

english, 2015

12

Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene

Jacobson, Samuel G., Cideciyan, Artur V., Sumaroka, Alexander, Roman, Alejandro J., Charng, Jason, Lu, Monica, Choi, Windy, Sheplock, Rebecca, Swider, Malgorzata, Kosyk, Mychajlo S., Schwartz, Sharon

Journal:

Investigative Opthalmology & Visual Science

Year:

2017

Language:

english

File:

PDF, 1.84 MB

english, 2017

13

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

Cideciyan, Artur V., Jacobson, Samuel G., Drack, Arlene V., Ho, Allen C., Charng, Jason, Garafalo, Alexandra V., Roman, Alejandro J., Sumaroka, Alexander, Han, Ian C., Hochstedler, Maria D., Pfeifer,

Journal:

Nature Medicine

Year:

2018

Language:

english

File:

PDF, 7.18 MB

english, 2018

14

Inner Retinal Abnormalities in X-linked Retinitis Pigmentosa with RPGR Mutations

Aleman, Tomas S., Cideciyan, Artur V., Sumaroka, Alexander, Schwartz, Sharon B., Roman, Alejandro J., Windsor, Elizabeth A. M., Steinberg, Janet D., Branham, Kari, Othman, Mohammad, Swaroop, Anand, Ja

Journal:

Investigative Ophthalmology & Visual Science

Year:

2007

Language:

english

File:

PDF, 599 KB

english, 2007

15

Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerations

Cideciyan, Artur V., Swider, Malgorzata, Aleman, Tomas S., Roman, Marisa I., Sumaroka, Alexander, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.

Journal:

Journal of the Optical Society of America A

Year:

2007

Language:

english

File:

PDF, 926 KB

english, 2007

16

Treatment Possibilities for Retinitis Pigmentosa

Jacobson, Samuel G., Cideciyan, Artur V.

Journal:

Boston Medical and Surgical Journal

Year:

2010

Language:

english

File:

PDF, 577 KB

english, 2010

17

Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of disease

Beltran, William A., Cideciyan, Artur V., Iwabe, Simone, Swider, Malgorzata, Kosyk, Mychajlo S., McDaid, Kendra, Martynyuk, Inna, Ying, Gui-Shuang, Shaffer, James, Deng, Wen-Tao, Boye, Sanford L., Lew

Journal:

Proceedings of the National Academy of Sciences

Year:

2015

Language:

english

File:

PDF, 2.27 MB

english, 2015

18

Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene

Aguirre, Geoffrey K., Butt, Omar H., Datta, Ritobrato, Roman, Alejandro J., Sumaroka, Alexander, Schwartz, Sharon B., Cideciyan, Artur V., Jacobson, Samuel G.

Journal:

Investigative Opthalmology & Visual Science

Year:

2017

Language:

english

File:

PDF, 3.87 MB

english, 2017

19

Retinal Disease Expression in Bardet-Biedl Syndrome-1 ( BBS1 ) Is a Spectrum from Maculopathy to Retina-Wide Degeneration

Azari, Amir A., Aleman, Tomas S., Cideciyan, Artur V., Schwartz, Sharon B., Windsor, Elizabeth A. M., Sumaroka, Alexander, Cheung, Andy Y., Steinberg, Janet D., Roman, Alejandro J., Stone, Edwin M., S

Journal:

Investigative Ophthalmology & Visual Science

Year:

2006

Language:

english

File:

PDF, 553 KB

english, 2006

20

ABCA4 -Associated Retinal Degenerations Spare Structure and Function of the Human Parapapillary Retina

Cideciyan, Artur V., Swider, Malgorzata, Aleman, Tomas S., Sumaroka, Alexander, Schwartz, Sharon B., Roman, Marisa I., Milam, Ann H., Bennett, Jean, Stone, Edwin M., Jacobson, Samuel G.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2005

Language:

english

File:

PDF, 581 KB

english, 2005

21

Improvement in vision: a new goal for treatment of hereditary retinal degenerations

Jacobson, Samuel G, Cideciyan, Artur V, Aguirre, Gustavo D, Roman, Alejandro J, Sumaroka, Alexander, Hauswirth, William W, Palczewski, Krzysztof

Journal:

Expert Opinion on Orphan Drugs

Year:

2015

Language:

english

File:

PDF, 785 KB

english, 2015

22

[Methods in Enzymology] Vertebrate Phototransduction and the Visual Cycle, Part B Volume 316 || [41] In vivo assessment of photoreceptor function in human diseases caused by photoreceptor-specific gene mutations

Cideciyan, Artur V.

Year:

2000

Language:

english

File:

PDF, 846 KB

english, 2000

23

BEST1 gene therapy corrects a diffuse retina-wide microdetachment modulated by light exposure

Guziewicz, Karina E., Cideciyan, Artur V., Beltran, William A., Komáromy, András M., Dufour, Valerie L., Swider, Malgorzata, Iwabe, Simone, Sumaroka, Alexander, Kendrick, Brian T., Ruthel, Gordon, Chi

Journal:

Proceedings of the National Academy of Sciences

Year:

2018

Language:

english

File:

PDF, 2.12 MB

english, 2018

24

Treatment of Leber Congenital Amaurosis Due to RPE65 Mutations by Ocular Subretinal Injection of Adeno-Associated Virus Gene Vector: Short-Term Results of a Phase I Trial

Hauswirth, William W., Aleman, Tomas S., Kaushal, Shalesh, Cideciyan, Artur V., Schwartz, Sharon B., Wang, Lili, Conlon, Thomas J., Boye, Sanford L., Flotte, Terence R., Byrne, Barry J., Jacobson, Sam

Journal:

Human Gene Therapy

Year:

2008

Language:

english

File:

PDF, 518 KB

english, 2008

25

Pupillary Light Reflexes in Severe Photoreceptor Blindness Isolate the Melanopic Component of Intrinsically Photosensitive Retinal Ganglion Cells

Charng, Jason, Jacobson, Samuel G., Heon, Elise, Roman, Alejandro J., McGuigan, David B., Sheplock, Rebecca, Kosyk, Mychajlo S., Swider, Malgorzata, Cideciyan, Artur V.

Journal:

Investigative Opthalmology & Visual Science

Year:

2017

Language:

english

File:

PDF, 1.04 MB

english, 2017

26

EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression

McGuigan, David, Heon, Elise, Cideciyan, Artur, Ratnapriya, Rinki, Lu, Monica, Sumaroka, Alexander, Roman, Alejandro, Batmanabane, Vaishnavi, Garafalo, Alexandra, Stone, Edwin, Swaroop, Anand, Jacobso

Journal:

Year:

2017

Language:

english

File:

PDF, 6.98 MB

english, 2017

27

Photoreceptor Layer Topography in Children with Leber Congenital Amaurosis Caused by RPE65 Mutations

Jacobson, Samuel G., Cideciyan, Artur V., Aleman, Tomas S., Sumaroka, Alexander, Windsor, Elizabeth A. M., Schwartz, Sharon B., Heon, Elise, Stone, Edwin M.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2008

Language:

english

File:

PDF, 415 KB

english, 2008

28

Translational Retinal Research and Therapies

Hardcastle, Alison J., Sieving, Paul A., Sahel, José-Alain, Jacobson, Samuel G., Cideciyan, Artur V., Flannery, John G., Beltran, William A., Aguirre, Gustavo D.

Journal:

Translational Vision Science & Technology

Year:

2018

Language:

english

File:

PDF, 974 KB

english, 2018

29

RPGR- Associated Retinal Degeneration in Human X-Linked RP and a Murine Model

Huang, Wei Chieh, Wright, Alan F., Roman, Alejandro J., Cideciyan, Artur V., Manson, Forbes D., Gewaily, Dina Y., Schwartz, Sharon B., Sadigh, Sam, Limberis, Maria P., Bell, Peter, Wilson, James M., S

Journal:

Investigative Ophthalmology & Visual Science

Year:

2012

Language:

english

File:

PDF, 5.07 MB

english, 2012

30

Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations

Jacobson, Samuel G., McGuigan, David B., Sumaroka, Alexander, Roman, Alejandro J., Gruzensky, Michaela L., Sheplock, Rebecca, Palma, Judy, Schwartz, Sharon B., Aleman, Tomas S., Cideciyan, Artur V.

Journal:

Investigative Opthalmology & Visual Science

Year:

2016

Language:

english

File:

PDF, 3.54 MB

english, 2016

31

Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal rats

Tomas S. Aleman, Matthew M. LaVail, Rodrigo Montemayor, Gui-shuang Ying, Maureen M. Maguire, Alan M. Laties, Samuel G. Jacobson, Artur V. Cideciyan

Journal:

Vision Research

Year:

2001

Language:

english

File:

PDF, 349 KB

english, 2001

32

Efficacy Outcome Measures for Clinical Trials of USH2A caused by the Common c.2299delG Mutation

Calzetti, Giacomo, Levy, Richard A., Cideciyan, artur v., Garafalo, Alexandra V., Roman, Alejandro J., Sumaroka, Alexander, Charng, Jason, Heon, Elise, Jacobson, Samuel G.

Journal:

American Journal of Ophthalmology

Year:

2018

Language:

english

File:

PDF, 7.60 MB

english, 2018

33

Imaging Lenticular Autofluorescence in Older Subjects

Charng, Jason, Tan, Rose, Luu, Chi D., Sadigh, Sam, Stambolian, Dwight, Guymer, Robyn H., Jacobson, Samuel G., Cideciyan, Artur V.

Journal:

Investigative Opthalmology & Visual Science

Year:

2017

Language:

english

File:

PDF, 795 KB

english, 2017

34

Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations

Sumaroka, Alexander, Matsui, Rodrigo, Cideciyan, Artur V., McGuigan, David B., Sheplock, Rebecca, Schwartz, Sharon B., Jacobson, Samuel G.

Journal:

Investigative Opthalmology & Visual Science

Year:

2016

Language:

english

File:

PDF, 1.96 MB

english, 2016

35

TULP1 Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

Jacobson, Samuel G., Cideciyan, Artur V., Huang, Wei Chieh, Sumaroka, Alexander, Roman, Alejandro J., Schwartz, Sharon B., Luo, Xunda, Sheplock, Rebecca, Dauber, Joanna M., Swider, Malgorzata, Stone,

Journal:

Investigative Opthalmology & Visual Science

Year:

2014

Language:

english

File:

PDF, 1.60 MB

english, 2014

36

Human Retinal Disease from AIPL1 Gene Mutations: Foveal Cone Loss with Minimal Macular Photoreceptors and Rod Function Remaining

Jacobson, Samuel G., Cideciyan, Artur V., Aleman, Tomas S., Sumaroka, Alexander, Roman, Alejandro J., Swider, Malgorzata, Schwartz, Sharon B., Banin, Eyal, Stone, Edwin M.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2011

Language:

english

File:

PDF, 2.44 MB

english, 2011

37

Patterns of Individual Variation in Visual Pathway Structure and Function in the Sighted and Blind

Aguirre, Geoffrey K., Datta, Ritobrato, Benson, Noah C., Prasad, Sashank, Jacobson, Samuel G., Cideciyan, Artur V., Bridge, Holly, Watkins, Kate E., Butt, Omar H., Dain, Aleksandra S., Brandes, Lauren

Journal:

Year:

2016

Language:

english

File:

PDF, 2.42 MB

english, 2016

38

Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8

Fujinami, Kaoru, Strauss, Rupert W, Chiang, John (Pei-Wen), Audo, Isabelle S, Bernstein, Paul S, Birch, David G, Bomotti, Samantha M, Cideciyan, Artur V, Ervin, Ann-Margret, Marino, Meghan J, Sahel, J

Journal:

British Journal of Ophthalmology

Year:

2018

Language:

english

File:

PDF, 3.16 MB

english, 2018

39

Autosomal Dominant Retinitis Pigmentosa Due to Class B Rhodopsin Mutations: An Objective Outcome for Future Treatment Trials

Sumaroka, Alexander, Cideciyan, Artur V., Charng, Jason, Wu, Vivian, Powers, Christian A., Iyer, Bhavya S., Lisi, Brianna, Swider, Malgorzata, Jacobson, Samuel G.

Journal:

International Journal of Molecular Sciences

Year:

2019

Language:

english

File:

PDF, 2.72 MB

english, 2019

40

Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives

Garafalo, Alexandra V., Cideciyan, Artur V., Héon, Elise, Sheplock, Rebecca, Pearson, Alexander, WeiYang Yu, Caberry, Sumaroka, Alexander, Aguirre, Gustavo D., Jacobson, Samuel G.

Journal:

Progress in Retinal and Eye Research

Year:

2019

File:

PDF, 3.48 MB

2019

41

Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone function

Krishnan, Arun K., Jacobson, Samuel G., Roman, Alejandro J., Iyer, Bhavya S., Garafalo, Alexandra V., HÃ©on, Elise, Cideciyan, Artur V.

Journal:

Vision Research

Year:

2020

Language:

english

File:

PDF, 2.08 MB

english, 2020

42

The Enhanced S Cone Syndrome: An Analysis of Receptoral and Post-receptoral Changes

VIVIENNE C GREENSTEIN, QASIM ZAIDI, DONALD C HOOD, BRANKA SPEHAR, ARTUR V CIDECIYAN, SAMUEL G JACOBSON

Journal:

Vision Research

Year:

1996

Language:

english

File:

PDF, 2.38 MB

english, 1996

43

Pitfalls in Homozygosity Mapping

Maria G. Miano, Samuel G. Jacobson, Andrew Carothers, Isabel Hanson, Peter Teague, Jill Lovell, Artur V. Cideciyan, Neena Haider, Edwin M. Stone, Val C. Sheffield, Alan F. Wright

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 236 KB

english, 2000

44

Molecular Anthropology Meets Genetic Medicine to Treat Blindness in the North African Jewish Population: Human Gene Therapy Initiated in Israel

Banin, Eyal, Bandah-Rozenfeld, Dikla, Obolensky, Alexey, Cideciyan, Artur V., Aleman, Tomas S., Marks-Ohana, Devora, Sela, Malka, Boye, Sanford, Sumaroka, Alexander, Roman, Alejandro J., Schwartz, Sha

Journal:

Human Gene Therapy

Year:

2010

Language:

english

File:

PDF, 880 KB

english, 2010

45

Inner and Outer Retinal Changes in Retinal Degenerations Associated With ABCA4 Mutations

Huang, Wei Chieh, Cideciyan, Artur V., Roman, Alejandro J., Sumaroka, Alexander, Sheplock, Rebecca, Schwartz, Sharon B., Stone, Edwin M., Jacobson, Samuel G.

Journal:

Investigative Opthalmology & Visual Science

Year:

2014

Language:

english

File:

PDF, 1.21 MB

english, 2014

46

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies

Strauss, Rupert W., Ho, Alex, Muñoz, Beatriz, Cideciyan, Artur V., Sahel, José-Alain, Sunness, Janet S., Birch, David G., Bernstein, Paul S., Michaelides, Michel, Traboulsi, Elias I., Zrenner, Eberhar

Journal:

Year:

2016

Language:

english

File:

PDF, 2.08 MB

english, 2016

47

Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector

Cideciyan, Artur V., Sudharsan, Raghavi, Dufour, Valérie L., Massengill, Michael T., Iwabe, Simone, Swider, Malgorzata, Lisi, Brianna, Sumaroka, Alexander, Marinho, Luis Felipe, Appelbaum, Tatyana, Ro

Journal:

Proceedings of the National Academy of Sciences

Year:

2018

Language:

english

File:

PDF, 2.08 MB

english, 2018

48

Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion Mutations

Sumaroka, Alexander, Garafalo, Alexandra V., Cideciyan, Artur V., Charng, Jason, Roman, Alejandro J., Choi, Windy, Saxena, Supna, Aksianiuk, Valeryia, Kohl, Susanne, Wissinger, Bernd, Jacobson, Samuel

Journal:

Investigative Opthalmology & Visual Science

Year:

2018

Language:

english

File:

PDF, 2.22 MB

english, 2018

49

Dose Range Finding Studies with Two RPGR Transgenes in a Canine Model of X-linked Retinitis Pigmentosa Treated with Subretinal Gene Therapy

Song, Chunjuan, Dufour, Valerie L. L, Cideciyan, Artur V., Ye, Guo-jie, Swider, Malgorzata, Newmark, Judith, Timmers, Adrian, Robinson, Paulette, Knop, David R., Chulay, Jeffrey David, Jacobson, Samue

Journal:

Human Gene Therapy

Year:

2020

File:

PDF, 2.27 MB

2020

50

Genetics and Disease Expression in the CNGA3 Form of Achromatopsia

Zelinger, Lina, Cideciyan, Artur V., Kohl, Susanne, Schwartz, Sharon B., Rosenmann, Ada, Eli, Dalia, Sumaroka, Alexander, Roman, Alejandro J., Luo, Xunda, Brown, Cassondra, Rosin, Boris, Blumenfeld, A

Journal:

Year:

2015

Language:

english

File:

PDF, 1.69 MB

english, 2015

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