Results 151 to 160 of about 44,319 (309)
European Journal of Neurology, Volume 30, Issue 2, Page 511-526, February 2023., 2023 Abstract Background and purpose Charcot–Marie–Tooth disease (CMT) is a heterogeneous group of disorders caused by mutations in at least 100 genes. However, approximately 60% of cases with axonal neuropathies (CMT2) still remain without a genetic diagnosis. We aimed at identifying novel disease genes responsible for CMT2.
Silvia Cipriani +23 more
wiley +1 more source
Machine learning based white matter models with permeability: An experimental study in cuprizone treated in-vivo mouse model of axonal demyelination [PDF]
arXiv, 2019 The intra-axonal water exchange time {\tau}i, a parameter associated with axonal permeability, could be an important biomarker for understanding demyelinating pathologies such as Multiple Sclerosis. Diffusion-Weighted MRI is sensitive to changes in permeability, however, the parameter has remained elusive due to the intractability of the mathematical ...
arxiv
Axonal degeneration and inflammation in acute optic neuritis [PDF]
, 2004 Aims: To investigate whether plasma biomarkers for axonal injury and inflammation are related to loss and recovery of visual function in acute optic neuritis (ON).Methods: Eighteen patients with ON and 14 controls were investigated in a longitudinal ...
Petzold, A, Plant, GT, Rejdak, K
core +2 more sources
Ibrain, EarlyView.We report a girl with a diagnosis of “neuromyelitis optica spectrum disorder comorbid Sjogren's syndrome” whose condition showed significant improvement after treatment with corticosteroids and immunosuppressive drugs (prednisolone, hydroxychloroquine, and mycophenolate mofetil).
Man‐Min Zhu +3 more
wiley +1 more source
European Journal of Neurology, Volume 30, Issue 2, Page 463-473, February 2023., 2023 In this study we define long‐term characteristics of various neurological autoimmune disorders encountered after SARS‐CoV‐2 vaccinations. Long‐term outcome was favorable in most cases. Re‐vaccinations were well‐tolerated and should be considered on an individual risk/benefit analysis.
Sofia Doubrovinskaia +11 more
wiley +1 more source
“Swayback”: A Congenital Demyelinating Disease of Lambs with Affinities to Schilder's Encephalitis [PDF]
, 1936 J. R. M. Innes
openalex +1 more source
European Journal of Neurology, Volume 30, Issue 2, Page 399-412, February 2023., 2023 Abstract Background and purpose Clinical outcome information on patients with neuromuscular diseases (NMDs) who have been infected with SARS‐CoV‐2 is limited. The aim of this study was to determine factors associated with the severity of COVID‐19 outcomes in people with NMDs.
Chiara Pizzamiglio +93 more
wiley +1 more source
AX UNUSUAL CASE OF PRIMARY DEMYELINATING DISEASE [PDF]
, 1960 W Zeman, Frederick S. Sherman
openalex +1 more source
Five decades of cuprizone, an updated model to replicate demyelinating diseases [PDF]
, 2017 : Introduction: Demyelinating diseases of the central nervous system (CNS) comprise a group of neurological disorders characterized by progressive (and eventually irreversible) loss of oligodendrocytes and myelin sheaths in the white matter tracts.
GONZALEZ PEREZ, OSCAR +7 more
core
CSF oligoclonal bands in neurological diseases besides CNS inflammatory demyelinating disorders
BMJ Neurology OpenObjective To understand the distribution characteristics and clinical significance of cerebrospinal fluid (CSF) oligoclonal bands (OCBs) in different nervous system diseases besides typical central nervous system (CNS) inflammatory demyelinating ...
Feng Gao +6 more
doaj +1 more source