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Published in 2021 at "Journal of Neuroimmunology"
DOI: 10.1016/j.jneuroim.2020.577449
Abstract: BACKGROUND Plasma exchange (PE) has usually to be considered as a rescue therapy when intravenous corticosteroids is insufficient in acute attacks of neuromyelitis optica spectrum disorders (NMOSD). The efficacy of PE has not been quantified.…
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Keywords:
plasma exchange;
acute attacks;
efficacy;
therapy ... See more keywords
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Published in 2018 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2018.12.009
Abstract: INTRODUCTION Acute intermittent porphyria (AIP) is characterized by hepatic over-production of the heme precursors when aminolevulinic acid (ALA)-synthase 1 is induced by endogenous or environmental factors. The aim of this study was to develop a…
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Keywords:
acute intermittent;
intermittent porphyria;
disease model;
acute attacks ... See more keywords
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Published in 2017 at "Clinical and Experimental Neuroimmunology"
DOI: 10.1111/cen3.12394
Abstract: Neuromyelitis optica or neuromyelitis optica spectrum disorders (NMOSD) are autoimmune diseases associated with a disease‐specific autoantibody directed against the water channel protein aquaporin‐4. While almost all patients with NMOSD show a relapsing‐remitting course, just 2%…
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Keywords:
spectrum disorders;
acute attacks;
neuromyelitis optica;
optica spectrum ... See more keywords
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Published in 2022 at "European Journal of Neurology"
DOI: 10.1111/ene.15561
Abstract: Neuromyelitis optica spectrum disorder (NMOSD) is a severe neurological inflammatory disease mainly caused by pathogenic aquaporin‐4 antibodies (AQP4‐IgG). The safety and efficacy of the neonatal Fc receptor antagonist batoclimab addition to conventional intravenous methylprednisolone pulse…
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Keywords:
neuromyelitis optica;
acute attacks;
spectrum disorder;
optica spectrum ... See more keywords
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Published in 2019 at "Oral health & preventive dentistry"
DOI: 10.3290/j.ohpd.a42740
Abstract: PURPOSE C1-inhibitor (C1-INH) related hereditary angioedema (C1-INH-HAE) is a rare pathological condition caused by a deficiency or a functional alteration of serum protein C1-INH. Clinical manifestations are represented by recurrent, potentially life-threatening episodes of cutaneous…
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Keywords:
patients requiring;
inh;
treatment;
acute attacks ... See more keywords