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10.1111/ene.14368

http://scihub22266oqcxt.onion/10.1111/ene.14368
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32478936!7300656!32478936
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suck abstract from ncbi


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pmid32478936      Eur+J+Neurol 2020 ; 27 (9): 1751-1753
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  • SARS-CoV-2 and Guillain-Barre syndrome: AIDP variant with a favourable outcome #MMPMID32478936
  • Lascano AM; Epiney JB; Coen M; Serratrice J; Bernard-Valnet R; Lalive PH; Kuntzer T; Hubers A
  • Eur J Neurol 2020[Sep]; 27 (9): 1751-1753 PMID32478936show ga
  • BACKGROUND AND PURPOSE: The spectrum of COVID-19, caused by severe acute respiratory syndrome coronavirus 2 infection (SARS-CoV-2), includes different neurologic manifestations of the central and peripheral nervous system. METHODS: From March through April 2020, in two university hospitals located in western Switzerland, we examined three patients with Guillain-Barre syndrome (GBS) following SARS-CoV-2. RESULTS: These cases were characterized by a primary demyelinating electrophysiological pattern (Acute inflammatory demyelinating polyneuropathy or AIDP) and a less severe disease course compared to recently published case series. Clinical improvement was observed in all patients at week five. One patient was discharged from hospital after full recovery with persistence of minor neurological signs (areflexia). Two of the three patients remained hospitalized: one was able to walk and the other could stand up with assistance. CONCLUSIONS: We report three cases of typical GBS (AIDP) occurring after SARS-CoV-2 infection and presenting with a favourable clinical course. Given the interval between COVID-19-related symptoms and neurological manifestations (mean of 15 days) we postulate a secondary immune-mediated mechanism rather than direct viral damage.
  • |COVID-19/*complications[MESH]
  • |Disease Progression[MESH]
  • |Female[MESH]
  • |Guillain-Barre Syndrome/drug therapy/*etiology/physiopathology[MESH]
  • |Humans[MESH]
  • |Immunoglobulins, Intravenous/therapeutic use[MESH]
  • |Middle Aged[MESH]
  • |Neural Conduction/*physiology[MESH]
  • |Switzerland[MESH]


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