Results 101 to 110 of about 685,293 (263)
Optic Nerve Hypoplasia: Controversies in Embryogenesis
Optic nerve hypoplasia is the most common congenital optic disc anomaly encountered in clinical practice.IC-C6bv-hypoplastic-and-dysplastic-optic-nerve; IC-E1f-common-malformations-of-the-eye-and ...
Michael C. Brodsky
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Frequency and Phenotype of Coexisting Aquaporin‐4 and Autoimmune Encephalitis Autoantibodies
ABSTRACT Among 9457 aquaporin‐4 (AQP4) immunoglobulin G‐positive patients, 2071 underwent autoimmune encephalitis antibody testing and 85 (4%) had coexisting antibodies, most commonly cerebrospinal fluid glial fibrillary acidic protein‐IgG and N‐methyl‐D‐aspartate receptor‐IgG, or serum high‐titer GAD65‐IgG.
Laura Cacciaguerra +25 more
wiley +1 more source
The glymphatic system facilitates cerebrospinal fluid (CSF) circulation and metabolic waste clearance in the central nervous system. Its alterations and neuroprotective potentials in cerebral disorders also have been confirmed.
Yuning Zhang +11 more
doaj +1 more source
Glucagon‐Like Peptide‐1 Receptor Agonists in Multiple Sclerosis: A Topical Narrative Review
ABSTRACT The glucagon‐like peptide‐1 (GLP‐1) receptor agonists (RAs) are a relatively new class of drugs that were initially approved by the US Food and Drug Administration to improve glycemic control in patients with type 2 diabetes mellitus and, subsequently, weight reduction in patients with obesity.
Audrey Y. Chang, Farrah J. Mateen
wiley +1 more source
Involvement of High Mobility Group Box 1 Protein in Optic Nerve Damage in Diabetes
Ghulam Mohammad,1 Renu A Kowluru1,2 1Department of Ophthalmology, Visual and Anatomical Sciences, Wayne State University, Detroit, MI, 48201, USA; 2Kresge Eye Institute, Wayne State University, Detroit, MI, 48201, USACorrespondence: Ghulam Mohammad, Tel +
Mohammad G, Kowluru RA
doaj
Investigation of Complement Activation and Cytokine Signatures in AQP4+ NMOSD, MOGAD, and MS
ABSTRACT Objective Aquaporin‐4‐IgG seropositive neuromyelitis optica spectrum disorder (AQP4+ NMOSD), myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD), and multiple sclerosis (MS) are pathophysiologically distinct neuroinflammatory disorders. Complement activation is a major mechanism of injury in AQP4+ NMOSD, whereas its role in
Angeliki G. Filippatou +23 more
wiley +1 more source
Efficacy of Fampridine on Refractory Optic Neuritis in Neuromyelitis Optica Spectrum Disorders
ABSTRACT Background Neuromyelitis optica spectrum disorders (NMOSD) usually occur with acute refractory optic neuritis (ON). However, there is a lack of efficacious treatments to improve recovery. Since fampridine has been found to improve the prognosis of multiple sclerosis (MS) and MS‐related ON, it is necessary to explore the efficacy of fampridine ...
Hongxuan Wang +9 more
wiley +1 more source
ABSTRACT Background Biallelic FIG4 variants classically cause distinct conditions characterized by peripheral neuropathy (Charcot‐Marie‐Tooth disease type 4J) or skeletal dysplasia (Yunis‐Varón syndrome). However, central nervous system involvement is increasingly recognized. The prevalence and specific characteristics of movement disorders within FIG4‐
Andrea Gangfuß +22 more
wiley +1 more source
Optic Nerve and Optic Nerve Sheath Biopsy Indications and Outcomes
Optic nerve and nerve sheath biopsy (ONB/ONSB) are diagnostic tests considered for optic nerve disease when other investigations have failed to provide a diagnosis.
Reilly Coombs; John Chen; Diva Salomao; Deena Tajfirouz; Eric Eggenberger; Marie DiNome; Jacqueline Leavitt; Misha Pless; James Garrity; Sasha Mansukhani
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Optic Nerve Developmental Abnormalities
Developmental abnormalities of the optic disc frequently herald the presence of additional malformations within the brain. A classification system for developmental optic disc abnormalities is valuable because many optic disc malformations correlate with
Michael C. Brodsky
core

