Results 221 to 230 of about 4,362,153 (359)

Visual impairment and blindness in Hungary

Acta ophthalmologica, 2018
Dorottya Szabó, Gábor L Sándor, Gábor Tóth, Anita Pék, Regina Lukács, I. Szalai, G. Tóth, A. Papp, Z. Nagy, H. Limburg, J. Németh   +10 more
semanticscholar   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

Instruments for Assessing Health-Related Quality of Life in People With Visual Impairment: Protocol for a Scoping Review. [PDF]

JMIR Res Protoc
Alves Ribeiro AF, Ferreira Júnior MA, Moraes da Silva A, Lima Meza L, Alvaro Menezes BK.   +4 more
europepmc   +1 more source

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

Guillain-Barré Syndrome and Visual Impairment Associated with Emerging Oropouche Virus Lineage, Brazil, 2024. [PDF]

Emerg Infect Dis
Filho CG, Carvalho FMM, Neto ASL, Maia AMC, Rossi MA, Pitombeira MS, Matos PCAAP, Coelho TMS, Neto LVP, de Almeida LM, Naveca FG, de Oliveira CS, de Bruycker-Nogueira F, de Filippis AMB, Luz KG, Ribas Freitas AR, de Góes Cavalcanti LP.   +16 more
europepmc   +1 more source

Unraveling 4‐Phenylbutyrate's Therapeutic Role in SLC6A1 Disorders: Pharmacochaperoning Over HDAC Inhibition

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw, Karishma Randhave, Ekta Anand, Ziang (Debbie) Song, Wangzhen Shen, Jing‐Qiong Kang   +5 more
wiley   +1 more source

Carers' recognition of concurrent visual impairment in dementia. [PDF]

J Alzheimers Dis
Tyler SL, Paterson KB, Hutchinson CV.
europepmc   +1 more source

Subclinical Optic Nerve Involvement in Radiologically Isolated Syndrome: Multimodal Detection and Diagnostic Impact

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We aimed to determine the frequency of subclinical optic nerve (ON) lesions using MRI, optical coherence tomography (OCT), and visual evoked potentials (VEP) in radiologically isolated syndrome (RIS), and to assess their diagnostic and prognostic significance.
Christine Lebrun‐Frenay, Cassandre Landes‐Château, Lydiane Mondot, Mikael Cohen, Margherita Popolo, Jérôme de Seze, Bertrand Bourre, Françoise Durand‐Dubief, Olivier Casez, Orhun H. Kantarci, Aksel Siva, Stephanie Baillif, Darin T. Okuda, Letizia Leocani   +13 more
wiley   +1 more source

DIAPH1 regulates the Wnt/β-catenin pathway resulting in microcephaly and visual impairment. [PDF]

BMC Med Genomics
Wang D, Lai P, Wang K, Wu Z, Li X.
europepmc   +1 more source

Association of Axial Length With Risk of Uncorrectable Visual Impairment for Europeans With Myopia.

JAMA ophthalmology, 2016
J. Tideman, Margaretha C. C. Snabel, M. Tedja, Gwyneth A. van Rijn, King T. Wong, R. Kuijpers, J. Vingerling, A. Hofman, Gabriëlle H S Buitendijk, J. Keunen, C. Boon, A. Geerards, G. Luyten, V. Verhoeven, C. Klaver   +14 more
semanticscholar   +1 more source