Works matching DE "NIGHT blindness"

Results: 93

Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?

Published in:

Documenta Ophthalmologica, 2018, v. 137, n. 2, p. 87, doi. 10.1007/s10633-018-9653-y

By:

Oh, Annie;
Loew, Ellis R.;
Foster, Melanie L.;
Davidson, Michael G.;
English, Robert V.;
Gervais, Kristen J.;
Herring, Ian P.;
Mowat, Freya M.

Publication type:

Article

Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.

Published in:

Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 57, doi. 10.1007/s10633-018-9651-0

By:

Marmor, Michael F.;
Zeitz, Christina

Publication type:

Article

ISCEV extended protocol for the photopic On-Off ERG.

Published in:

Documenta Ophthalmologica, 2018, v. 136, n. 3, p. 199, doi. 10.1007/s10633-018-9645-y

By:

Sustar, Maja;
Holder, Graham E.;
Kremers, Jan;
Barnes, Claire S.;
Lei, Bo;
Khan, Naheed W.;
Robson, Anthony G.

Publication type:

Article

Phenotypic expansion and progression of <italic>SPATA7</italic>-associated retinitis pigmentosa.

Published in:

2018

By:

Sengillo, Jesse D.;
Lee, Winston;
Bilancia, Colleen G.;
Jobanputra, Vaidehi;
Tsang, Stephen H.

Publication type:

Case Study

Recurrent episodes of night blindness in a patient with short bowel syndrome.

Published in:

Documenta Ophthalmologica, 2015, v. 131, n. 3, p. 221, doi. 10.1007/s10633-015-9516-8

By:

Renner, Agnes;
Dietrich-Ntoukas, Tina;
Jägle, Herbert

Publication type:

Article

Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations.

Published in:

Documenta Ophthalmologica, 2015, v. 131, n. 1, p. 71, doi. 10.1007/s10633-015-9497-7

By:

Kuniyoshi, Kazuki;
Sakuramoto, Hiroyuki;
Yoshitake, Kazutoshi;
Ikeo, Kazuho;
Furuno, Masaaki;
Tsunoda, Kazushige;
Kusaka, Shunji;
Shimomura, Yoshikazu;
Iwata, Takeshi

Publication type:

Article

Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy.

Published in:

Documenta Ophthalmologica, 2015, v. 130, n. 3, p. 231, doi. 10.1007/s10633-015-9484-z

By:

Saker, Saker;
Morales, Marco;
Jhittay, Harsimar;
Wen, Yaqin;
Amoaku, Winfried

Publication type:

Article

Estimating ON and OFF contributions to the photopic hill: normative data and clinical applications.

Published in:

Documenta Ophthalmologica, 2014, v. 129, n. 1, p. 9, doi. 10.1007/s10633-014-9446-x

By:

Garon, M.-L.;
Dorfman, A.;
Racine, J.;
Koenekoop, R.;
Little, J.;
Lachapelle, P.

Publication type:

Article

Editor's comment.

Published in:

2013

By:

Brodie, Scott

Publication type:

Editorial

Xerophthalmia and acquired night blindness in a patient with a history of gastrointestinal neoplasia and normal serum vitamin A levels.

Published in:

Documenta Ophthalmologica, 2013, v. 126, n. 2, p. 159, doi. 10.1007/s10633-012-9370-x

By:

Anastasakis, Anastasios;
Plainis, Sotiris;
Giannakopoulou, Trisevgeni;
Papadimitraki, Elisavet;
Fanouriakis, Charalambos;
Tsilimbaris, Miltiadis

Publication type:

Article

Negative electroretinograms in the pediatric and adult population.

Published in:

Documenta Ophthalmologica, 2012, v. 124, n. 1, p. 41, doi. 10.1007/s10633-011-9301-2

By:

Kim, Johnstone;
Payne, John;
Yan, Jiong;
Barnes, Claire

Publication type:

Article

Macular Neovascularization in a Patient with Pigmented Paravenous Chorioretinal Atrophy.

Published in:

Türkiye Klinikleri Journal of Case Reports, 2023, v. 31, n. 2, p. 63, doi. 10.5336/caserep.2022-94394

By:

BODUR, Muhiddin Fatih;
KOÇAK, Nurullah

Publication type:

Article

Smart Night-Vision Glasses with AI and Sensor Technology for Night Blindness and Retinitis Pigmentosa.

Published in:

International Journal of Advanced Computer Science & Applications, 2025, v. 16, n. 2, p. 962, doi. 10.14569/ijacsa.2025.0160295

By:

Qazi, Shaheer Hussain;
Batumalay, M.

Publication type:

Article

A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness.

Published in:

Genes, 2021, v. 12, n. 2, p. 171, doi. 10.3390/genes12020171

By:

Mahmood, Usman;
Méjécase, Cécile;
Ali, Syed M. A.;
Moosajee, Mariya;
Kozak, Igor;
Sieving, Paul A.

Publication type:

Article

Metabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes.

Published in:

Pigment Cell & Melanoma Research, 2013, v. 26, n. 3, p. 348, doi. 10.1111/pcmr.12083

By:

Devi, Sulochana;
Markandeya, Yogananda;
Maddodi, Nityanand;
Dhingra, Anuradha;
Vardi, Noga;
Balijepalli, Ravi C.;
Setaluri, Vijayasaradhi

Publication type:

Article

Ocular Fundus Imaging for the Diagnosis of Progressive Retinal Atrophy - A Study in 31 Dogs.

Published in:

Intas Polivet, 2016, v. 17, n. 2, p. 426

By:

Kelawala, D. N.;
Patil, D. B.;
Sini, K. R.;
Parikh, P. V.;
Parulekar, E. A.

Publication type:

Article

Utilizing Zebrafish Visual Behaviors in Drug Screening for Retinal Degeneration.

Published in:

International Journal of Molecular Sciences, 2017, v. 18, n. 6, p. 1185, doi. 10.3390/ijms18061185

By:

Logan Ganzen;
Venkatraman, Prahatha;
Chi Pui Pang;
Yuk Fai Leung;
Mingzhi Zhang

Publication type:

Article

Network and Atomistic Simulations Unveil the Structural Determinants of Mutations Linked to Retinal Diseases.

Published in:

PLoS Computational Biology, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pcbi.1003207

By:

Mariani, Simona;
Dell'Orco, Daniele;
Felline, Angelo;
Raimondi, Francesco;
Fanelli, Francesca

Publication type:

Article

Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50573-7

By:

Das, Rueben G.;
Becker, Doreen;
Jagannathan, Vidhya;
Goldstein, Orly;
Santana, Evelyn;
Carlin, Kendall;
Sudharsan, Raghavi;
Leeb, Tosso;
Nishizawa, Yuji;
Kondo, Mineo;
Aguirre, Gustavo D.;
Miyadera, Keiko

Publication type:

Article

Extensive Macular Atrophy with Pseudodrusen Imaged with OCT Angiography.

Published in:

2018

By:

Kovach, Jaclyn L.

Publication type:

Case Study

Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness.

Published in:

Clinical Ophthalmology, 2016, v. 10, p. 1593, doi. 10.2147/OPTH.S99593

By:

Cammack, Jocelyn;
Whight, John;
Cross, Vinette;
Rider, Andrew T.;
Webster, Andrew R.;
Stockman, Andrew

Publication type:

Article

Infrared imaging enhances retinal crystals in Bietti's crystalline dystrophy.

Published in:

2015

By:

Brar, Vikram S.;
Benson, William H.

Publication type:

Case Study

Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness.

Published in:

2013

By:

Xue Tan;
Aya Aoki;
Yasuo Yanagi

Publication type:

Case Study

Electrophysiological findings in Oguchi disease.

Published in:

2013

By:

de Mendonça, Regina Halfeld Furtado;
Abbruzzese, Stefania;
Plateroti, Rocco;
Plateroti, Pasquale;
Lucia Ferreira, Eliana

Publication type:

Case Study

RIM1/2-Mediated Facilitation of Cav1.4 Channel Opening Is Required for Ca<sup>2+</sup>-Stimulated Release in Mouse Rod Photoreceptors.

Published in:

Journal of Neuroscience, 2015, v. 35, n. 38, p. 13133, doi. 10.1523/JNEUROSCI.0658-15.2015

By:

Grabner, Chad P.;
Gandini, Maria A.;
Rehak, Renata;
Yun Le;
Zamponi, Gerald W.;
Schmitz, Frank

Publication type:

Article

GPR179 Is Required for High Sensitivity of the mGluR6 Signaling Cascade in Depolarizing Bipolar Cells.

Published in:

Journal of Neuroscience, 2014, v. 34, n. 18, p. 6334, doi. 10.1523/JNEUROSCI.4044-13.2014

By:

Ray, Thomas A.;
Heath, Kathryn M.;
Hasan, Nazarul;
Noel, Jennifer M.;
Samuels, Ivy S.;
Martemyanov, Kirill A.;
Peachey, Neal S.;
McCall, Maureen A.;
Gregg, Ronald G.

Publication type:

Article

An association between subclinical familial exudative vitreoretinopathy and rod-cone dystrophy.

Published in:

2014

By:

ILHAN, ABDULLAH;
YOLCU, UMIT;
GUNDOGAN, FATIH CAKIR;
AKAY, FAHRETTIN

Publication type:

Case Study

Retinoids as chemopreventive agents.

Published in:

2016

By:

Kaur, Sandeep

Publication type:

journal article

Onchocerciasis as a Risk Factor for Night Blindness.

Published in:

Ophthalmic Epidemiology, 2012, v. 19, n. 4, p. 204, doi. 10.3109/09286586.2012.680529

By:

Babalola, O. E.

Publication type:

Article

HLA-A29-positive Birdshot Chorioretinopathy in a Hispanic Patient.

Published in:

2016

By:

Baddar, Dina;
Goldstein, Debra A.

Publication type:

Case Study

A Case Report of Vogt's Limbal Girdle and Retinitis Pigmentosa in a Thirteen-Year-Old Boy: A Rare and Unusual Association.

Published in:

Case Reports in Ophthalmology, 2015, v. 6, n. 3, p. 311, doi. 10.1159/000439265

By:

Vignesh, A.P.;
Srinivasan, Renuka;
Karanth, Swathi;
Vijitha, Sai

Publication type:

Article

Multiple congenital ocular anomalies and the silver dapple gene.

Published in:

Equine Veterinary Education, 2013, v. 25, n. 11, p. 556, doi. 10.1111/eve.12099

By:

Matthews, A. G.

Publication type:

Article

A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient.

Published in:

Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0324-6

By:

Siying Liang;
Nan Jiang;
Shuo Li;
Xiaohu Jiang;
Dongyi Yu

Publication type:

Article

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.

Published in:

Eye, 2012, v. 26, n. 9, p. 1278, doi. 10.1038/eye.2012.125

By:

Vincent, A;
Héon, E

Publication type:

Article

I Cannot Read as Well...My Speech Is Slower and Writing Now Poor.

Published in:

Journal of Pediatric Ophthalmology & Strabismus, 2017, v. 54, n. 3, p. 138, doi. 10.3928/01913913-20170412-01

By:

Tang, Alice R.;
Walton, David S.

Publication type:

Article

Mizuo Nakamura Phenomenon.

Published in:

2015

By:

Kumar, Vinod;
Walton, David S.

Publication type:

Case Study

Black Dots and the Evil Eye!

Published in:

2015

By:

Nair, Akshay Gopinathan;
Trivedi, Mihir G.;
Shirwadkar, Shruti P.;
Potdar, Nayana A.;
Shinde, Chhaya A.;
Walton, David S.

Publication type:

Case Study

Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy.

Published in:

2016

By:

Méjécase, Cécile;
Laurent-Coriat, Caroline;
Mayer, Claudine;
Poch, Olivier;
Mohand-Saïd, Saddek;
Prévot, Camille;
Antonio, Aline;
Boyard, Fiona;
Condroyer, Christel;
Michiels, Christelle;
Blanchard, Steven;
Letexier, Mélanie;
Saraiva, Jean-Paul;
Sahel, José-Alain;
Audo, Isabelle;
Zeitz, Christina

Publication type:

Case Study

Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.

Published in:

Graefe's Archive of Clinical & Experimental Ophthalmology, 2016, v. 254, n. 10, p. 1951, doi. 10.1007/s00417-016-3346-6

By:

Oreany, Abdulaziz;
Hadlaq, Abdulaziz;
Schatz, Patrik

Publication type:

Article

Determinants of gestational night blindness in pregnant women from Rio de Janeiro, Brazil.

Published in:

2016

By:

Saunders, Cláudia;
Leal, Maria do Carmo;
Neves, Paulo Augusto Ribeiro;
Padilha, Patricia de Carvalho;
da Silva, Letícia Barbosa Gabriel;
Schilithz, Arthur Orlando Corrêa;
Saunders, Cláudia;
da Silva, Letícia Barbosa Gabriel;
Schilithz, Arthur Orlando Corrêa

Publication type:

journal article

Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families.

Published in:

Human Genome Variation, 2020, v. 7, n. 1, p. 1, doi. 10.1038/s41439-020-0100-8

By:

Nadeem, Raheela;
Kabir, Firoz;
Li, Jiali;
Gradstein, Libe;
Jiao, Xiaodong;
Rauf, Bushra;
Naeem, Muhammad Asif;
Assir, Muhammad Zaman;
Riazuddin, Sheikh;
Ayyagari, Radha;
Hejtmancik, J. Fielding;
Riazuddin, S. Amer

Publication type:

Article

Novel gene mutation in a patient with Bietti crystalline dystrophy without corneal deposits.

Published in:

2017

By:

Raoof, Naz;
Vincent, Andrea L

Publication type:

Case Study

Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.

Published in:

Clinical Genetics, 2016, v. 89, n. 6, p. 690, doi. 10.1111/cge.12746

By:

Neuillé, M.;
Malaichamy, S.;
Vadalà, M.;
Michiels, C.;
Condroyer, C.;
Sachidanandam, R.;
Srilekha, S.;
Arokiasamy, T.;
Letexier, M.;
Démontant, V.;
Sahel, J.‐A.;
Sen, P.;
Audo, I.;
Soumittra, N.;
Zeitz, C.

Publication type:

Article

Diagnóstico de la ceguera nocturna mediante entrevista normalizada y electrorretinografía.

Published in:

2020

By:

Elaine Pereira, Silvia;
José Saboya, Carlos;
Carvalho de Jesus, Patricia;
Cruz, Sabrina;
Ramalho, Andréa;
Pereira, Sílvia;
Saboya, Carlos;
Jesus, Patrícia;
Cruz, Sabrina Pereira da

Publication type:

journal article

Vitamin A deficiency is associated with body mass index and body adiposity in women with recommended intake of vitamin A.

Published in:

2018

By:

Bento, Claudia;
Matos, Andréa C.;
Cordeiro, Adryana;
Ramalho, Andréa

Publication type:

journal article

The use of handheld spectral domain optical coherence tomography in pediatric ophthalmology practice: Our experience of 975 infants and children.

Published in:

2015

By:

Mallipatna, Ashwin;
Vinekar, Anand;
Jayadev, Chaitra;
Dabir, Supriya;
Sivakumar, Munsusamy;
Krishnan, Narasimha;
Mehta, Pooja;
Berendschot, Tos;
Yadav, Naresh Kumar

Publication type:

journal article

Desferrioxamine-related ocular toxicity: A case report.

Published in:

Indian Journal of Ophthalmology, 2012, v. 60, n. 4, p. 315, doi. 10.4103/0301-4738.98714

By:

Simon, Sumu;
Athanasiov, Paul A.;
Jain, Rajeev;
Raymond, Grant;
Gilhotra, Jagjit S.

Publication type:

Article

Night blindness, diet and health in Nepalese children: An ethno‐epidemiological investigation of local beliefs.

Published in:

Ecology of Food & Nutrition, 2000, v. 39, n. 3, p. 199, doi. 10.1080/03670244.2000.9991615

By:

Shankar, Anita V.;
Gittelsohn, Joel;
Pradhan, Rajendra;
Dahal, Birendra;
West, Keith P.

Publication type:

Article

Isotretinoin and night blindness.

Published in:

Australasian Journal of Dermatology, 2014, v. 55, n. 3, p. 222, doi. 10.1111/ajd.12107

By:

Teo, Ken;
Yazdabadi, Anousha

Publication type:

Article

Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-75902-z

By:

Kim, You Na;
Song, Joon Seon;
Oh, Seak Hee;
Kim, Yoon Jeon;
Yoon, Young Hee;
Seo, Eul-Ju;
Seol, Chang Ahn;
Lee, Sae-Mi;
Choi, Jong-Moon;
Seo, Go Hun;
Keum, Changwon;
Lee, Beom Hee;
Lee, Joo Yong

Publication type:

Article