Results 191 to 200 of about 94,021 (297)
Journal of the Peripheral Nervous System, Volume 31, Issue 4, December 2026.ABSTRACT Background and Aims Maple syrup urine disease (MSUD) is an inherited disorder of branched‐chain amino acid metabolism caused by deficiency of the branched‐chain α‐keto acid dehydrogenase complex. Neurological manifestations predominantly involve the central nervous system, whereas peripheral nervous system involvement has been rarely reported.
Gustavo Rodrigues Ferreira Gomes +7 more
wiley +1 more source
The FASEB Journal, Volume 40, Issue 21, 15 November 2026.Concomitant burn injury and blast‐induced mild TBI lead to a magnified neuroimmune response shaped by endocrine stress‐related pathways and IL‐1R1‐dependent inflammatory signals, which also produce cytokine‐mediated impairment of erythropoiesis. These integrated systemic and CNS responses illustrate how inflammation, hematopoietic adaptation, and early
Hana C. Schwierling +7 more
wiley +1 more source
Annals of Neurology, Volume 100, Issue 5, Page 1039-1054, November 2026.Repeat expansion disorders frequently involve peripheral neuropathy, yet mechanisms remain unclear. Using a spinocerebellar ataxia type 3 (SCA3) Knock‐In Atxn3Q300/Q6, we identify progressive sensorimotor deficits, peripheral nerve pathology, and dorsal root ganglia RNA splicing dysregulation.
Juan P. Mato +7 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 11, November 2026.ABSTRACT The diagnosis of Guillain–Barré syndrome (GBS) relies on evolving clinical features, supported by cerebrospinal fluid (CSF), laboratory investigations, and electrodiagnostic studies. Early investigations may be nondiagnostic and should not delay treatment when progressive neurological deterioration raises clinical suspicion of GBS.
Rhiana Pereira‐Lindley +2 more
wiley +1 more source
The Neurovascular Niche: A Gathering Venue for Neuroinflammation and Remyelination in Multiple Sclerosis. [PDF]
Acta Physiol (Oxf)Kazanis I +4 more
europepmc +1 more source