Results 91 to 100 of about 103,129 (245)

Mycotic Sphenopalatine Sinusitis With Concurrent Compression of the Optic Nerves and Chiasm and Severe Visual Impairment in A Horse

Veterinary Ophthalmology, Volume 29, Issue 1, January 2026.
ABSTRACT A 15‐year‐old Swiss Warmblood gelding was presented to the ophthalmology service of Zurich University due to severe visual impairment. Ophthalmic and neurologic examinations were performed, raising suspicion of post‐retinal blindness. Standing contrast computed tomography (CT) of the head revealed a partially calcified, soft tissue attenuating
Niklas Holz, José Suárez, Udo Hetzel, Antonella Rampazzo, Riccardo Stoppini   +4 more
wiley   +1 more source

An Interesting Case of Blau Syndrome – A Rare Autoinflammatory Disease

Indian Journal of Medical Specialities
Blau syndrome is an autosomal dominant, autoinflammatory disease. It typically presents in early childhood with a triad of granulomatous uveitis, symmetrical arthritis, and dermatitis.
Swapan Nagpal, Veer Singh
doaj   +1 more source

Patterns of uveitis at a tertiary referral center in Northeastern Iran

Journal of Ophthalmic & Vision Research, 2018
Purpose: To describe the demographic and clinical patterns of patients with uveitis referred to a tertiary center in northeastern Iran. Methods: This cross-sectional retrospective study included 235 patients with uveitis who had been referred to the ...
Seyedeh Maryam Hosseini, Nasser Shoeibi, Raheleh Ebrahimi, Mehdi Ghasemi   +3 more
doaj   +1 more source

A Misleading Diagnosis of Sarcoidosis in an Older Woman [PDF]

Common variable immunodeficiency (CVID) is the most frequent primary immunodeficiency and has a reported prevalence of approximately 1:25,000 to 1:50,000.
Allaoui, Abire, Bouissar, Wassila, Echchilali, Khadija, Elkabli, Hassan, Moudatir, Mina, Zahra Alaoui, Fatim   +5 more
core   +1 more source

A 66‐year‐old man with acute retinal necrosis

Brain Pathology, Volume 36, Issue 2, March 2026.
Shino Magaki, Fausto J. Rodriguez, Matthew Koo, Colin A. McCannel   +3 more
wiley   +1 more source

Early Optic Nerve Symptoms in Neurosarcoidosis: A Clinical Case Review

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Neurosarcoidosis is a rare and often misdiagnosed condition. It should be considered in patients with unexplained neurological symptoms, especially when associated with systemic inflammatory findings. Early diagnosis and immunosuppressive therapy are crucial to prevent irreversible neurological damage.
Isabella Passarelli Giabardo Marques, Caio Henrique Peres Oliani, Nicoli Lopes de Oliveira, Jade Pinto de Queiroz Guerra, Guilherme Lopes Coelho, Guilherme de Oliveira Aurich, Marcello Novoa Colombo Barboza, Priscilla Fernandes Nogueira   +7 more
wiley   +1 more source

NOD2 and inflammation: current insights [PDF]

, 2018
The nucleotide-binding oligomerization domain (NOD) protein, NOD2, belonging to the intracellular NOD-like receptor family, detects conserved motifs in bacterial peptidoglycan and promotes their clearance through activation of a proinflammatory ...
Cucchiara, Salvatore, Negroni, Anna, Pierdomenico, Maria, Stronati, Laura   +3 more
core   +2 more sources

Relationship between Helicobacter pylori and idiopathic non-granulomatous anterior uveitis [PDF]

, 2022
Héctor Javier Pérez-Cano, Jimena Ceja-Martínez, Vanessa Tellezgiron-Lara, S. Voorduin-Ramos, Óscar Morales-López, Selma Alin Somilleda-Ventura   +5 more
openalex   +1 more source

Vasculitis associated with Ehrlichia canis and Babesia canis in a dog in the Netherlands

Veterinary Record Case Reports, Volume 13, Issue 4, December 2025.
Abstract This report describes a case of severe, sudden‐onset, widespread vasculitis affecting a dog concurrently infected by Ehrlichia canis and Babesia canis. Following diagnostic investigations, the dog was suspected of an immune‐mediated vasculitis, possibly triggered by E. canis, B. canis or their combination. The lesions completely resolved after
Thomas Dijkxhoorn, Silvia T. Auxilia, Marie Welters, Nathalie De Vries, Margreet Ploeg   +4 more
wiley   +1 more source

A New Mutation in Blau Syndrome

Case Reports in Rheumatology, 2015
Blau syndrome is a rare, autosomal dominant, granulomatous autoinflammatory disease. The classic triad of the disease includes recurrent uveitis, granulomatous dermatitis, and symmetrical arthritis.
Cengiz Zeybek, Gokalp Basbozkurt, Davut Gul, Erkan Demirkaya, Faysal Gok   +4 more
doaj   +1 more source