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Clinical features of LRP4/agrin-antibody-positive myasthenia gravis: A multicenter study.
Muscle & Nerve ( IF 2.8 ) Pub Date : 2020-06-01 , DOI: 10.1002/mus.26985
Michael H Rivner 1 , Brandy M Quarles 1 , Jin-Xiu Pan 2 , Zheng Yu 2 , James F Howard 3 , Andrea Corse 4 , Mazen M Dimachkie 5 , Carlayne Jackson 6 , Tuan Vu 7 , George Small 8 , Robert P Lisak 9 , Jerry Belsh 10 , Ikjae Lee 11 , Richard J Nowak 12 , Vanessa Baute 13 , Stephen Scelsa 14 , J Americo Fernandes 15 , Zachary Simmons 16 , Andrea Swenson 17 , Richard Barohn 5 , R Bhavaraju Sanka 6 , Clifton Gooch 7 , Eroboghene Ubogu 11 , James Caress 13 , Mamatha Pasnoor 5 , Hongyan Xu 18 , Lin Mei 2
Affiliation  

Our aim in this study was to identify the prevalence and clinical characteristics of LRP4/agrin‐antibody–positive double‐seronegative myasthenia gravis (DNMG).

中文翻译:

LRP4 / agrin抗体阳性重症肌无力的临床特征:一项多中心研究。

我们在这项研究中的目的是鉴定LRP4 / agrin抗体阳性的双血清阴性重症肌无力(DNMG)的患病率和临床特征。
更新日期:2020-06-01
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