Results 61 to 70 of about 184,937 (258)

Transverse myelitis in myelin oligodendrocyte glycoprotein antibody-associated disease

open access: yesFrontiers in Neurology, 2023
Transverse myelitis (TM) is the second most common presentation of myelin oligodendrocyte antibody-associated disease (MOGAD), occurring in approximately 26% of affected patients.
Gina Perez-Giraldo   +2 more
doaj   +1 more source

Myelin Oligodendrocyte Glycoprotein Antibody Associated Cerebral Cortical Encephalitis: Case Reports and Review of Literature

open access: yesFrontiers in Human Neuroscience, 2022
Myelin oligodendrocyte glycoprotein antibody-associated disease is an immune-mediated demyelinating disease of the central nervous system that is present in both adults and children.
Hang Shu   +5 more
semanticscholar   +1 more source

Clinical spectrum of myelin oligodendrocyte glycoprotein antibody-associated disease in Brazil: a single-center experience

open access: yesArquivos de Neuro-Psiquiatria, 2023
Background Anti-myelin oligodendrocyte glycoprotein (anti-MOG) antibody-associated disease (MOGAD) is an immune-mediated neurological disorder with a broad spectrum of clinical presentation that is often difficult to distinguish from other ...
Katharina Messias   +6 more
doaj   +1 more source

Devic mouse: a spontaneous double-transgenic mouse model of human opticospinal multiple sclerosis and autoimmune T- B cell cooperation [PDF]

open access: yes, 2007
Multiple sclerosis (MS) is an autoimmune inflammatory disease of the central nervous system (CNS). Myelin antigen(s) specific T cells, B cells, and antibodies are thought to play a role in the pathogenesis of MS.
Krishnamoorthy, Gurumoorthy
core   +1 more source

Myelin oligodendrocyte glycoprotein antibody-associated disease as a novel presentation of central nervous system autoimmunity in a pediatric patient with Wiskott-Aldrich syndrome

open access: yesAllergy, Asthma & Clinical Immunology, 2023
Background Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency caused by mutations in the WAS gene that leads to increased susceptibility to infections, thrombocytopenia, eczema, malignancies, and autoimmunity.
Vivien X. Xie   +6 more
doaj   +1 more source

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease: Current Insights into the Disease Pathophysiology, Diagnosis and Management

open access: yesInternational Journal of Molecular Sciences, 2020
Myelin oligodendrocyte glycoprotein (MOG)-associated disease (MOGAD) is a rare, antibody-mediated inflammatory demyelinating disorder of the central nervous system (CNS) with various phenotypes starting from optic neuritis, via transverse myelitis to ...
W. Ambrosius   +3 more
semanticscholar   +1 more source

Clinico‐radiological characteristics of anti‐myelin oligodendrocyte glycoprotein antibody‐associated autoimmune encephalitis in children

open access: yesDevelopmental Medicine & Child Neurology, 2022
To investigate the clinical characteristics and prevalence of paediatric anti‐myelin oligodendrocyte glycoprotein (MOG) antibody‐associated autoimmune encephalitis.
Ji-Ye-On Han   +8 more
semanticscholar   +1 more source

Radiological characteristics of myelin oligodendrocyte glycoprotein antibody disease [PDF]

open access: yesMultiple Sclerosis and Related Disorders, 2019
MOG antibody disease is an autoimmune disease of the central nervous system (CNS) characterized by the presence of a serological antibody against myelin oligodendrocyte glycoprotein (MOG). MRI is instrumental in distinguishing neuromyelitis optica spectrum disorder (NMOSD) from multiple sclerosis (MS), but MRI features of MOG disease appear to overlap ...
Sara Salama   +3 more
openaire   +2 more sources

Phenotypic characteristics of myelin oligodendrocyte glycoprotein antibody-associated disease in children: a single-center, retrospective study

open access: yesFrontiers in Neurology, 2023
ObjectiveTo analyze the clinical characteristics and follow-up data of children with different clinical phenotypes of myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD).MethodsThe basic demographic and clinical features, laboratory ...
Yi Hua   +7 more
doaj   +1 more source

Clinicopathological Features of Pakistani Patients with Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease (MOGAD)

open access: yesPakistan Armed Forces Medical Journal
Objective: To characterize clinicopathological features of patients with Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease in local population for early diagnosis and treatment. Study Design: Cross-sectional study.
Muhammad Zain Arshad   +5 more
doaj   +1 more source

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