Results 11 to 20 of about 2,133 (164)

Transient Dyschromatopsia, Static Form Agnosia, and Prosopagnosia Observed in a Patient with Anti-NMDA Receptor Encephalitis

Case Reports in Neurological Medicine, 2019
We presented a case of a 19-year-old woman who suffered from anti-N-methyl-D-aspartate (NMDA) receptor encephalitis associated with ovarian teratoma.
Ritsuo Hashimoto, Asako Tagawa, Noriyo Komori, Tomoko Ogawa, Hiroyuki Kato   +4 more
doaj   +2 more sources

Color faded glasses and quality of life improvement in color blindness

The Pan-American Journal of Ophthalmology
Background and Objectives: To assess the results of a pre- and post-lens quality of life (QoL) questionnaire. Determine the effect of glasses with a faded red filter on the degree of severity of the Hardy, Rand and Rittler (HRR) Richmond test in color ...
Luis A. Rodríguez-Gutiérrez, Irving A. Domínguez-Varela, Miguel A. Hernández-Delgado, Héctor J. Morales-Garza, Yolanda Macías-Rodríguez   +4 more
doaj   +2 more sources

Application of the international criteria for optic neuritis in the Acute Optic Neuritis Network

Annals of Clinical and Translational Neurology
Objective The first international consensus criteria for optic neuritis (ICON) were published in 2022. We applied these criteria to a prospective, global observational study of acute optic neuritis (ON). Methods We included 160 patients with a first‐ever
Philipp Klyscz, Susanna Asseyer, Ricardo Alonso, Charlotte Bereuter, Omer Bialer, Atira Bick, Sara Carta, John J. Chen, Leila Cohen, Yamit Cohen‐Tayar, Edgar Carnero Contentti, Russell C. Dale, Eoin P. Flanagan, Jonathan A. Gernert, Julian Haas, Joachim Havla, Christoph Heesen, Mark Hellmann, Netta Levin, Pablo Lopez, Itay Lotan, Maria Belen Luis, Sara Mariotto, Christina Mayer, Alvaro Jose Mejia Vergara, Cassandra Ocampo, Susana Ochoa, Frederike C. Oertel, Maja Olszewska, José Luis Peralta Uribe, Jaume Sastre‐Garriga, Dario Scocco, Sudarshini Ramanathan, Natthapon Rattanathamsakul, Fu‐Dong Shi, Jemal Shifa, Ilya Simantov, Sasitorn Siritho, Alon Tiosano, Nanthaya Tisavipat, Isabel Torres, Adi Vaknin Dembinsky, Angela Vidal‐Jordana, Adi Wilf‐Yarkoni, Ti Wu, Sol Zamir, Luis Alfonso Zarco, Hanna G. Zimmermann, Axel Petzold, Friedemann Paul, Hadas Stiebel‐Kalish   +50 more
doaj   +2 more sources

Neuroretinitis Secondary to Toxoplasma Infection in an Adult. [PDF]

Case Rep Ophthalmol Med
Purpose The purpose of this study is to report a case of neuroretinitis in a healthy adult with active primary Toxoplasma infection. Methods This study is a case report. Results A 27‐year‐old previously healthy woman presented with sudden‐onset blurred vision and a central scotoma in her left eye.
Ladak S, Siddiqui MAR.
europepmc   +2 more sources

Postoperative bilateral visual loss after a single dose of tranexamic acid. [PDF]

Anaesth Rep
Summary A 32‐year‐old woman presented with transient visual loss following the intra‐operative administration of a single intravenous dose of tranexamic acid during urgent cholecystectomy. Apart from obesity, the patient had no notable medical history or pre‐existing ocular conditions.
Chevalley B, Betello M, Blavakis E, Malclès A, Maillard J.   +4 more
europepmc   +2 more sources

A 51-year-old female presenting with headache and vision loss. [PDF]

Headache
Headache: The Journal of Head and Face Pain, Volume 66, Issue 8, Page 1928-1932, September 2026.
Ovrom L, Pardieck Z, Bowen RC, Cherayil NR.   +3 more
europepmc   +2 more sources

Idiopathic Paracentral Acute Middle Maculopathy in a Healthy Pregnant Woman: A Case Report. [PDF]

Case Rep Ophthalmol Med
Purpose The purpose of this study is to report a case of idiopathic paracentral acute middle maculopathy (PAMM) in a healthy woman during the first trimester of an uncomplicated pregnancy. Observations A 28‐year‐old woman at 14 weeks gestation presented with sudden onset of a paracentral scotoma in her right eye.
Broniarek K, Michalska-Małecka K.
europepmc   +2 more sources

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature Review. [PDF]

Mov Disord Clin Pract
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Yoganathan S, Tochen L, Ganguly J, Chowdhury SR, AlFaris HS, Pai V, LeBlanc-Millar A, Breitbart S, Kumar H, Shroff M, Reginald A, Yoon G, Fasano A, Ibrahim GM, Gorodetsky C.   +14 more
europepmc   +2 more sources

A review on today’s burden affecting the quality of life for colour blind patients [PDF]

Romanian Journal of Neurology, 2020
1.3 billion people worldwide suffer from a kind of visual impairment. Color blindness (dyschromatopsia) is a visual impairment affecting the quality of life for these patients and is estimated to be the highest in the male population of the European ...
Corina-Iuliana Suciu, Vlad-Ioan Suciu, Lacramioara Perju-Dumbrava, Simona Delia Nicoara   +3 more
doaj   +1 more source

Cerebral trauma-induced dyschromatopsia in the left hemifield: case presentation

BMC Ophthalmology, 2021
Background Acquired color anomalies caused by cerebral trauma are classified as either achromatopsias or dyschromatopsias (Zeki, Brain 113:1721–1777, 1990).
Yoko Mase, Yoshitsugu Matsui, Eriko Uchiyama, Hisashi Matsubara, Masahiko Sugimoto, Akiko Kubo, Mineo Kondo   +6 more
doaj   +1 more source