Results 71 to 80 of about 2,542 (166)
We described a multidisciplinary “sandwich” regimen combining preconception B‐cell depletion, gestational AZA‐steroid bridging and postpartum retreatment. In 7 of 8 AQP4‐IgG‐positive NMOSD women, this strategy achieved good maternal relapse control, together with favorable fetal safety and normal infant neurodevelopment within one‐year follow‐up ...
Li Xiao +17 more
wiley +1 more source
ABSTRACT Background and Aim Clinically isolated syndrome (CIS) may represent the earliest clinical manifestation of multiple sclerosis (MS). Cognitive and psychological impairments may appear during the early phase of CIS, even in the absence of significant neurological disability.
Sahar Jamshidi +4 more
wiley +1 more source
After a recent NMOSD attack, serum GFAP and age together provide a simple and powerful way to distinguish AQP4‐IgG NMOSD from MOGAD and related disorders. In 240 patients evaluated within 90 days of an attack from a 640‐patient cohort, this combination achieved high diagnostic accuracy (AUC up to 0.95).
Manon Rival +57 more
wiley +1 more source
Longitudinally extensive transverse myelitis with mycobacterium tuberculosis infection [PDF]
Le Fang +5 more
openaire +2 more sources
A case of tubercular meningoencephalitis with transverse myelitis
Central nervous system tuberculosis accounts for approximately 1% of all tuberculosis cases. Transverse myelitis is an extremely rare manifestation of central nervous system tuberculosis, involving 1 or more vertebral segments of the spinal cord. However,
Abhikanta Khatiwada, MD +3 more
doaj +1 more source
Longitudinally Extensive Transverse Myelitis With and Without Aquaporin 4 Antibodies
Aquaporin 4 antibody (AQP4-Ab)-negative patients with longitudinally extensive transverse myelitis (LETM) behave differently from those with AQP4-Ab. Aquaporin 4 antibody-negative neuromyelitis optica (NMO) is rare when good assays are used.To assess if AQP4-Ab-negative patients with LETM share similar disease characteristics with AQP4-Ab-positive ...
Kitley, J +8 more
openaire +2 more sources
Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis [PDF]
Leber Hereditary Optic Neuropathy is an inherited optic neuropathy caused by mitochondrial DNA point mutations leading to sudden, painless loss of vision. We report a case of an 8-year-old boy presenting with a radiological phenotype of longitudinally extensive transverse myelitis on a background of severe visual impairment secondary to Leber ...
Bursle, C +7 more
openaire +5 more sources
Seronegative Neuromyelitis Optica Spectrum - The challenges on disease definition and pathogenesis
Neuromyelitis optica spectrum disorders (NMOSD) are characterized by severe optic neuritis and/or longitudinally extensive transverse myelitis, and some brain lesions are also unique to NMOSD.
Douglas Kazutoshi Sato +4 more
doaj +1 more source
Objective: The aim is to compare the retinal nerve fiber layer (RNFL) thickness of longitudinally extensive transverse myelitis (LETM) eyes without previous optic neuritis with that of healthy control subjects.
Prakash Kumar Sinha +9 more
doaj +1 more source
Longitudinally extensive transverse myelitis associated with scrub typhus: A case report
Rationale: Longitudinally extensive transverse myelitis (LETM) is a rare inflammatory demyelinating disease predominantly associated with autoimmune and inflammatory disorders.
Amit Kumar +2 more
doaj +1 more source

