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[Parsonage Turner syndrome associated with COVID-19: About 2 family cases].

作者信息

Cabrera Pivaral C E, Rincón Sánchez A R, Dávalos Rodríguez N O, Ramirez Garcia S A

机构信息

Departamento de Salud Pública, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.

Instituto de Biología Molecular y Terapia génica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, México.

出版信息

Neurologia. 2023 Jan-Feb;38(1):59-60. doi: 10.1016/j.nrl.2022.01.006. Epub 2022 Feb 3.

DOI:10.1016/j.nrl.2022.01.006
PMID:35132291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8810346/
Abstract
摘要

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本文引用的文献

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[Amyotrophic neuralgia secondary to Vaxzevria (AstraZeneca) COVID-19 vaccine].[接种阿斯利康新冠疫苗Vaxzevria后引发的肌萎缩性神经痛]
Neurologia. 2021 Sep;36(7):571-572. doi: 10.1016/j.nrl.2021.05.007. Epub 2021 Jun 3.
2
[Acute transverse myelitis following SARS-CoV-2 infection].[新型冠状病毒2型感染后的急性横贯性脊髓炎]
Neurologia. 2021 Sep;36(7):572-574. doi: 10.1016/j.nrl.2021.05.008. Epub 2021 Jun 3.
3
Palatopharyngeal vesicular enanthem, early finding of COVID-19.腭咽囊疱疹性口炎，COVID-19 的早期发现。
Cir Cir. 2021;89(5):692-693. doi: 10.24875/CIRU.21000279.
4
Parsonage-Turner syndrome post-infection by SARS-CoV-2: a case report.新型冠状病毒感染后引发的帕森奇-特纳综合征：一例病例报告
Neurologia (Engl Ed). 2021 Sep;36(7):568-571. doi: 10.1016/j.nrleng.2021.04.003. Epub 2021 Jul 22.
5
Pirfenidone: A novel hypothetical treatment for COVID-19.吡非尼酮：一种针对新型冠状病毒肺炎的新型假设性治疗方法。
Med Hypotheses. 2020 Nov;144:110005. doi: 10.1016/j.mehy.2020.110005. Epub 2020 Jun 17.
6
Why choose cyclosporin A as first-line therapy in COVID-19 pneumonia.为何选择环孢素A作为新冠肺炎的一线治疗药物。
Reumatol Clin. 2021 Nov;17(9):555-557. doi: 10.1016/j.reuma.2020.03.001. Epub 2020 Apr 16.
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Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families.美国家族中17q25上遗传性神经性肌萎缩（HNA）位点的奠基者效应及位点精细定位的证据。
Hum Genet. 2002 Feb;110(2):166-72. doi: 10.1007/s00439-001-0647-5. Epub 2001 Dec 18.
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Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.17号染色体q25区域遗传性神经性肌萎缩（HNA）基因座的遗传精细定位
Eur J Hum Genet. 1999 Dec;7(8):920-7. doi: 10.1038/sj.ejhg.5200384.