Results 201 to 210 of about 796,114 (289)

Hepato-ocular crosstalk: Bile acids bridging pathogenesis and therapy. [PDF]

iScience
Wang P, Xie J, Xiang F, Xiong S, Li Y, Xia B, Lin L, Peng Q.   +7 more
europepmc   +1 more source

Biomarkers of ocular surface disease using impression cytology [PDF]

, 2017
Aronni S, Baudouin C, Brignole F, Danjo Y, Eberwein P, Hagan S, Kurpińska M, Mocanu CL, Roy P, Shiraki Y, Suzanne Hagan   +10 more
core   +2 more sources

Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Long‐read sequencing and optical genome mapping technologies have the ability to detect large and complex structural variants. This has led to the discovery of novel pathogenic variants in neurodegenerative movement disorders. Thus, we aimed to systematically compare the SV detection capabilities of OGM and ONT in Parkinson's disease.
André Fienemann, Theresa Lüth, Susen Schaake, Carolin Gabbert, Marius Möller, Hauke Busch, Katja Lohmann, Jonas A. Gustafson, Danny E. Miller, Kensuke Daida, Manabu Funayama, Nobutaka Hattori, Samia Ben Sassi, Faycel Hentati, Matthew J. Farrer, Kristian K. Ullrich, Christine Klein, Joanne Trinh   +17 more
wiley   +1 more source

Discrete eyelid swelling caused by live subconjunctival Dirofilaria repens

Open Medicine, 2011
Jaksic Vesna, Mitic Nebojsa, Pavlovic Ivan, Vitosevic Zdravko, Mirkovic Milos, Zoric Lepsa, Stamenkovic Divna, Vuksa Dubravka, Đokić Olivera   +8 more
doaj   +1 more source

Microplastics exposures in cataract surgery and potential clinical concerns. [PDF]

Sci Rep
Choi YH, Song MS, Park N, Park SA, Jung J, Choi YH, Kim DH.   +6 more
europepmc   +1 more source

Vestibular Patient Journey: Insights From Vestibular Disorders Association (VeDA) Registry

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Vestibular symptoms impose a high burden of disability. Understanding real‐world diagnostic and treatment pathways can identify care gaps and guide interventions. We aimed to characterize symptom profiles, diagnostic trends, provider involvement, and treatment patterns in vestibular disorders.
Ali Rafati, Sami I. Nassar, Shaun A. Nguyen, Patricia L. Gerend, Michael C. Schubert, Michael T. Teixido, Frederick A. Godley, Joel A. Goebel, Cynthia A. Ryan, Habib G. Rizk, Amir Kheradmand   +10 more
wiley   +1 more source

Ocular manifestations of Clade Ib mpox in four South-Kivu health zones, Democratic Republic of the Congo. [PDF]

PLOS Glob Public Health
Ngoma DB, Ntererwa IN, Irenge AB, Mweze MC, Katoto PMC, Lupande DM, Fodjo JNS, Noë P, Otiti JS, Kabesha TB, Colebunders R, Van Dijck C, Liesenborghs L, Mbala-Kingebeni P, Yeh S, Mwanza JC.   +15 more
europepmc   +1 more source

Baseline Regional Cholinergic Denervation Predicts Cognitive Trajectories in Moderate Parkinson Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cognitive decline is a disabling and variable feature of Parkinson disease (PD). While cholinergic system degeneration is linked to cognitive impairments in PD, most prior research reported cross‐sectional associations. We aimed to fill this gap by investigating whether baseline regional cerebral vesicular acetylcholine transporter ...
Taylor Brown, Giulia Carli, Prabesh Kanel, Stiven Roytman, Jaimie Barr, Nicolaas I. Bohnen, Roger L. Albin   +6 more
wiley   +1 more source

Ion-activated mucoadhesive in situ gel incorporating terbinafine-loaded NLCs promotes ocular penetration and retention for enhanced fungal keratitis therapy. [PDF]

Mater Today Bio
Dong F, Liang Z, Yao X, Zhang Z, Tao Y, Chen H, Lu P, Xia H, Zhang J, Pu G, Zhou T.   +10 more
europepmc   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina, Anna Marcé‐Grau, Barbara Masotto, Marta Codina, Lamia BenJemaa, Yasmina Elaribi, Mónica Martinez‐Gallo, Roger Colobran, Angel Sanchez‐Montañez, Irene Valenzuela, Yoshiko Murakami, Alfons Macaya   +11 more
wiley   +1 more source