Results 21 to 30 of about 114,193 (236)

Low‐Dose naltrexone restored TRPM3 ion channel function in natural killer cells from long COVID patients

Frontiers in Molecular Biosciences
IntroductionLong COVID is a multisystemic condition that includes neurocognitive, immunological, gastrointestinal, and cardiovascular manifestations, independent of the severity or duration of the acute SARS-CoV-2 infection.
Etianne Martini Sasso, Etianne Martini Sasso, Etianne Martini Sasso, Natalie Eaton-Fitch, Natalie Eaton-Fitch, Peter Smith, Peter Smith, Katsuhiko Muraki, Katsuhiko Muraki, Sonya Marshall-Gradisnik, Sonya Marshall-Gradisnik   +10 more
doaj   +1 more source

Acute combined central and peripheral nervous system demyelination: a case report [PDF]

Kosin Medical Journal, 2018
Guillain-Barré syndrome (GBS) and acute disseminated encephalomyelitis (ADEM) are demyelinating neurologic disorders with different target organs. Although they share similar pathogenetic mechanism, reports of simultaneous occurrence of the 2 disorders ...
Young Eun Roh, Young Mi Kim
doaj   +1 more source

Auto-Reactive Th17-Cells Trigger Obsessive-Compulsive-Disorder Like Behavior in Mice With Experimental Autoimmune Encephalomyelitis

Frontiers in Immunology, 2018
Th17-lymphocytes are well known for their deleterious role in autoimmunity. But does the notoriety of this repertoire extend beyond autoimmunity? In the present study we employed experimental autoimmune encephalomyelitis as model system to study the role
Ravi Kant, Ravi Kant, Shweta Pasi, Shweta Pasi, Avadhesha Surolia, Avadhesha Surolia   +5 more
doaj   +1 more source

Encephalomyelitis Caused by Balamuthia mandrillaris in a Woman With Breast Cancer: A Case Report and Review of the Literature

Frontiers in Immunology, 2022
Balamuthia mandrillaris is one cause of a rare and severe brain infection called granulomatous amoebic encephalitis (GAE), which has a mortality rate of >90%. Diagnosis of Balamuthia GAE is difficult because symptoms are non-specific.
Juan Hu, Yiqi Zhang, Yongwei Yu, Huili Yu, Siruo Guo, Ding Shi, Jianqin He, Chi Hu, Jiqi Yang, Xueling Fang, Yonghong Xiao   +10 more
doaj   +1 more source

Fatal Infection with Murray Valley Encephalitis Virus Imported from Australia to Canada, 2011

Emerging Infectious Diseases, 2017
Murray Valley encephalitis virus (MVEV), a flavivirus belonging to the Japanese encephalitis serogroup, can cause severe clinical manifestations in humans.
Daniel J. Niven, Kevin Afra, Mircea Iftinca, Raymond Tellier, Kevin Fonseca, Andreas Kramer, David Safronetz, Kimberly Holloway, Michael Drebot, Andrew S. Johnson   +9 more
doaj   +1 more source

Excellent Response to Plasma Exchange in Three Patients With Enterovirus-71 Neurological Disease

Frontiers in Neurology, 2019
The clinical spectrum of Enterovirus-71-associated neurological disease includes acute flaccid paralysis, encephalomyelitis, or brainstem encephalitis with autonomic dysfunction.
Elba Pascual-Goñi, Maria Josa, Cristian Launes, Luis Querol, Marga del Cuerpo, M. Alba Bosch, Iolanda Jordan, Iolanda Jordan, Eulàlia Turón-Viñas   +8 more
doaj   +1 more source

Guidelines for diagnosis and treatment in neurology – Lyme neuroborreliosis

GMS German Medical Science, 2020
Lyme borreliosis is the most common tick-borne infectious disease in Europe. A neurological manifestation occurs in 3–15% of infections and can manifest as polyradiculitis, meningitis and (rarely) encephalomyelitis.This S3 guideline is directed at ...
Rauer, Sebastian, Kastenbauer, Stephan, Hofmann, Heidelore, Fingerle, Volker, Huppertz, Hans-Iko, Hunfeld, Klaus-Peter, Krause, Andreas, Ruf, Bernhard, Dersch, Rick, Consensus group   +9 more
doaj   +1 more source

Four Human Cases of Eastern Equine Encephalitis in Connecticut, USA, during a Larger Regional Outbreak, 2019

Emerging Infectious Diseases, 2021
During 3 weeks in 2019, 4 human cases of Eastern equine encephalitis (EEE) were diagnosed at a single hospital in Connecticut, USA. The cases coincided with notable shifts in vector–host infection patterns in the northeastern United States and signified ...
Stacy C. Brown, Justine Cormier, Jessica Tuan, Audun J. Lier, Declan McGuone, Philip M. Armstrong, Firas Kaddouh, Sunil Parikh, Marie Louise Landry, Kevin T. Gobeske   +9 more
doaj   +1 more source

Understanding Further the Phenotypic Spectrum of Central Nervous System Inflammatory Demyelinating Disorders Using Unsupervised Clustering

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Central nervous system (CNS) inflammatory demyelinating syndromes, including multiple sclerosis (MS), aquaporin‐4 antibody–positive neuromyelitis optica spectrum disorder (AQP4 + NMOSD), and myelin oligodendrocyte glycoprotein (MOG) antibody–associated disease (MOGAD), occasionally overlap.
Bade Gulec, Elif Everest, Melih Tutuncu, Ugur Bilge, Sabahattin Saip, Ugur Uygunoglu, Aksel Siva   +6 more
wiley   +1 more source

Ofatumumab in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease: A Comparison With Rituximab

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate the efficacy and safety of ofatumumab in patients with myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), and compare it with rituximab. Methods We conducted a single–center, observational study including 22 MOGAD patients treated with ofatumumab and 21 treated with rituximab.
Yuxin Fan, Lei Zhou, Jingzi ZhangBao, Hongmei Tan, Zhouzhou Wang, Chao Quan   +5 more
wiley   +1 more source