Results 61 to 70 of about 3,766 (196)

The Mediating Effect of Inflammatory Biomarkers in the Associations Between Sarcoidosis and Incident Ischemic Stroke: A Prospective Cohort Study

open access: yesBrain and Behavior, Volume 16, Issue 4, April 2026.
Can invasive suckermouth catfish, Hypostomus plecostomus, be used as fishmeal? A potential solution to eradicate it from the Buriganga River, Bangladesh ABSTRACT Background and objective Sarcoidosis, characterized by granulomatous inflammation across multiple systems, has an unclear connection with ischemic stroke and shared molecular pathways.
Zihong Bai   +7 more
wiley   +1 more source

Diagnostic value of soluble Interleukin-2 receptor in patients suffering neurosarcoidosis: A systematic review

open access: yesJournal of Central Nervous System Disease
Background Neurosarcoidosis is an inflammatory granulomatous disease. Up to 25% of occult sarcoidosis affecting the nervous system are only detected by autopsy. In addition, in recent years the suspicion arose that the soluble Interleukin-2 Receptor (sIL-
Aditya Chanpura   +3 more
doaj   +1 more source

Rare Case of Spinal Neurosarcoidosis with Concomitant Epidural Lipomatosis

open access: yesCase Reports in Neurological Medicine, 2021
Introduction. Spinal neurosarcoidosis is a rare disease that can manifest as myelopathy, radiculopathy, or cauda equine syndrome. Spinal epidural lipomatosis is also a rare condition resulting from overgrowth of epidural fat tissue causing compressive ...
Nesreen Jaafar   +3 more
doaj   +1 more source

Head and Neck Manifestations in Sarcoidosis: An All of Us Research Program Matched Case‐Control Study

open access: yesOTO Open, Volume 10, Issue 2, April-June 2026.
Abstract Objective This study aims to assess the prevalence of head and neck (ENT) symptoms in patients with sarcoidosis. Study Design 1:4 matched‐case control study. Setting Patients with and without sarcoidosis who enrolled in the All of Us Research Program and consented to electronic medical record use.
Peter J. Attia   +6 more
wiley   +1 more source

Neurosarcoidosis [PDF]

open access: yes, 2022
Neurosarcoidosis (NS) affects 5-10% of sarcoidosis patients and can involve any part of the nervous system. The prognosis can be serious and relapse is common.
Yavarian, Yousef; id_orcid   +4 more
core   +2 more sources

The Kappa Free Light Chains Index in Multiple Sclerosis: From Emerging Evidence to Clinical Application

open access: yesJournal of Neurochemistry, Volume 170, Issue 4, April 2026.
This prospective study addresses the need for efficient multiple sclerosis (MS) biomarkers by validating a biological diagnostic algorithm. Based on paired cerebrospinal fluid (CSF) and serum samples from derivation and validation cohorts, the algorithm integrates the kappa free light chain (KFLC) index and oligoclonal bands (OCBs).
Noé Verchere   +9 more
wiley   +1 more source

Neurosarcoidosis

open access: yes, 2020
This is an illustrated guide to the clinical diagnosis of neurosarcoidosis. Sarcoidosis is a chronic systemic inflammatory disorder characterized by non-caseating granulomas.
Bryce Buchowicz, MD; Valérie Biousse, MD
core  

Neurosarcoidosis and MOG-associated Disease

open access: yes, 2022
Myelin oligodendrocyte glycoprotein (MOG) is a protein found on the surface of myelin, and anti-MOG antibodies can be elevated in demyelinating conditions such as multiple sclerosis, neuromyelitis optica spectrum disorder, or other MOG- associated ...
Sahar Noorani; Alden Gregston; Justin Bishop; Lauren Tardo; Melanie Truong-Le
core  

Application of the modified Zajicek criteria to diagnose probable spinal cord neurosarcoidosis

open access: yesClinical Case Reports, 2018
Key Clinical Message Neurosarcoidosis represents a significant diagnostic challenge, as clinical features overlap with other neuroinflammatory conditions, and biopsy of affected neuronal tissue is often high risk or not feasible.
Ceris Ifan Owen   +2 more
doaj   +1 more source

Clinical, biological and cytometric characteristics of two patients with a homozygous A91V PRF1 mutation

open access: yesClinical &Translational Immunology, Volume 15, Issue 3, 2026.
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare, inherited granzyme–perforin system defect that predisposes individuals to haemophagocytic lymphohistiocytosis. This article presents two original case reports of FHL type 2, along with a comprehensive literature review. Together, these elements aim to enhance the current understanding of FHL
Nicolas Perrard   +12 more
wiley   +1 more source

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