Sexual problems associated with neurological diseases (Neurosexology) European Federation of Neurological Societies Task Force on Neurosexology*. ? Lundberg PO Swash M, Vodusek D B ? Correspondence to P O Lundberg Department of Neuroscience: Neurology University Hospital Uppsala SE-751 85 Sweden Tel + 46 18 611 50 26 Fax + 46 18 611 50 27 E-mail: PO.Lundberg@neurologi.uu.se ? ? *The following text is based on Guidelines for Neurologists about Sexual problems associated with neurological diseases (Neurosexology) compiled by the members of the European Federation of Neurological Societies Task Force on Neurosexology published in 2001.
Aquaporin-4 (AQP4) exists as two major isoforms that differ in the length of the N terminus, the shorter AQP4-M23 and the longer AQP4-M1. Both isoforms form tetramers, which can further aggregate in the plasma membrane to form typical orthogonal arrays of particles (OAPs) whose dimension depends on the ratio of the M1 and M23. In this study, we tested the hypothesis that the M23 isoform can be produced directly by the M1 mRNA
Objective: Clinical studies indicate that anti-CD20 B-cell depletion may be an effective multiple sclerosis (MS) therapy. We investigated mechanisms of anti-CD20-mediated immune modulation using 2 paradigms of experimental autoimmune encephalomyelitis (EAE). Methods: Murine EAE was induced by recombinant myelin oligodendrocyte glycoprotein (rMOG), a model in which B cells are considered to contribute pathogenically, or MOG peptide (p)35-55, which does not require B cells.
OBJECTIVES: Longitudinal myelitis in patients with Sjogren’s syndrome (SS) is a rarely reported occurrence. Here, we present a patient with longitudinal myelitis who was found to have both primary SS and a positive antibody to aquaporin-4 (NMO-IgG). We review the recent literature concerning the overlap between primary SS-associated myelitis and the presence of NMO-IgG, suggestive of a neuromyelitis optica spectrum disorder (NMOSD).
There are no specific treatments for patients with acute, severe neurological deficits caused by neuromyelitis optica (NMO) who fail to recover after treatment with high-dose corticosteroids. We evaluated the clinical response of anti-tuberculosis treatment (ATT) in patients suffering from steroid-refractory NMO, and investigated the correlation between NMO and tuberculous infection of the central nervous system (CNS)