Results 91 to 100 of about 46,238 (244)

1‐Year Clinical Outcome Post‐Myasthenic Crisis: A Multicenter Prospective Study in China

European Journal of Neurology, Volume 33, Issue 2, February 2026.
In this prospective cohort of 282 patients with myasthenic crisis (MC) episodes, all‐cause mortality was 15.16%. Among 247 patients who have completed 1‐year follow‐up, 79.76% achieved favorable outcomes with significant improvement in the MG‐activities of daily living (MG‐ADL) score.
Xiao Huan, Ran Chen, Lei Jin, Yuan Wang, Yafang Xu, Lei Yang, Caihua Xi, Jianming Zheng, Lijun Luo, Song Yang, Jianquan Shi, Yanping Liu, Zhe Ruan, Wanlong Wu, Wei Li, Yaoxian Yue, Yarong Li, Wenji Jia, Huahua Zhong, Chong Yan, Jie Song, Jianying Xi, Song Tan, Qilong Jiang, Zhangyu Zou, Chongbo Zhao, Sushan Luo, on behalf of the Chinese Myasthenia Gravis Collaborating Group (CMGCG), Yuzhou Guan, Yuwei Da, Huan Yang, Ting Chang, Yuge Wang, Bitao Bu, Hongyu Zhou, Chunsheng Yang, Hua Zhang, Hui Deng, Ruisheng Duan   +38 more
wiley   +1 more source

Changes in lymphocyte subsets in patients with Guillain-Barré syndrome treated with immunoglobulin [PDF]

, 2014
BACKGROUND: Guillain-Barré syndrome (GBS) is an autoimmune condition characterized by peripheral neuropathy. The pathogenesis of GBS is not fully understood, and the mechanism of how intravenous immunoglobulin (IVIG) cures GBS is ambiguous.
Hui Qing Hou, Jun Miao, Li Guo, Mei Han, Xiu Juan Song, Xue Dan Feng   +5 more
core   +1 more source

New‐onset autoimmune disease following SARS‐CoV‐2 infection and mRNA vaccination in Norway: A retrospective cohort study

Journal of Internal Medicine, Volume 299, Issue 2, Page 271-282, February 2026.
Abstract Background Studies suggest an increase in autoimmune diseases following SARS‐CoV‐2 infection and/or COVID‐19‐vaccination. We aimed to describe possible associations in Norway. Methods We used information from the emergency preparedness register for COVID‐19, BeredtC19, for all residents aged 18–64 (N = 3,450,080).
Håkon Bøås, Paz Lopez‐Doriga Ruiz, Jesper Dahl, Hanne L. Gulseth, German Tapia   +4 more
wiley   +1 more source

Miller Fisher syndrome with sinus arrest [PDF]

, 2017
journal ...
ENOMOTO Tsuyoshi, Hoshino Sachiko, Kusunoki Susumu, Ohkoshi Norio, Shiraiwa Nobuko, TAMAOKA Akira, Umesawa Mitsumasa   +6 more
core   +2 more sources

Guillain-Barre Syndrome in a Patient With Asymptomatic Coronavirus Disease 2019 Infection and Major Depressive Disorder [PDF]

, 2021
Nikita Mokhashi, Gowtham Narla, Christine Marchionni   +2 more
openalex   +1 more source

From Barns to Bushes: Exploring the ECOFF‐Based Non‐Wild‐Type Status of Campylobacter spp. in Pets, Livestock, Synanthropic Birds and Wild Animals in Northwestern Italy

Zoonoses and Public Health, Volume 73, Issue 1, Page 30-44, February 2026.
ABSTRACT Introduction Antimicrobial resistance (AMR) poses a significant threat to both humans and animals. Zoonotic bacteria, such as Campylobacter, contribute to human infections and the spread of AMR, particularly through livestock, pets and wildlife. We investigated the prevalence, distribution and EUCAST ECOFF‐based wild‐type (WT) vs.
Aitor Garcia‐Vozmediano, Barbara Moroni, Cristina Marra, Monica Pitti, Giuliano Garofolo, Francesca Marotta, Roberta Di Romualdo, Simona Zoppi, Giuseppe Ru   +8 more
wiley   +1 more source

Intra‐ and Intermolecular Glycosylation of d‐Idopyranosyl and 6‐Deoxy‐d‐ido‐heptopyranosyl Donors: Toward the Repeating Unit of Campylobacter jejuni HS:4c Capsular Polysaccharide

European Journal of Organic Chemistry, Volume 29, Issue 4, January 26, 2026.
A comprehensive glycosylation study of diversely protected and activated d‐idopyranosyl and 6‐deoxy‐d‐ido‐heptopyranosyl donors using intra‐ and intermolecular coupling strategies is reported. Intramolecular aglycon delivery afforded 1,2‐cis‐β‐idopyranosides, while intermolecular glycosylation yielded chromatographically separable α‐ and β‐linked ...
Maude Cloutier, Nitish Verma, Ilona Douchez, Charles Gauthier   +3 more
wiley   +1 more source

An unusual presentation of gbs: case report and literature review [PDF]

, 2016
Guillain-Barre syndrome (GBS), also known as Landry paralysis is an acute idiopathic polyneuritis, believed to be immunologically mediated. It usually presents as a demyelinating neuropathy with ascending weakness, however, many clinical variants have ...
Badshah, Mazhar, Khattak, Irfan, Khattak, Sadaf, Nabi, Sumaira   +3 more
core   +1 more source

A Case of Neurobrucellosis Mimicking Guillain-Barre Syndrome

مجله دانشکده پزشکی اصفهان, 2007
BACKGROUND: Brucellosis is an infectious disease due to Gram negative bacteria of genus brucella. Involvement of different systems including gastrointestinal tract, the hepatobilliary and skeletal systems has been frequently reported.
Naser Sharafoddin Zadeh, Majid Keyhani Fard   +1 more
doaj  

Development of recurrent facial palsy during plasmapheresis in Guillain-Barré syndrome: a case report

Journal of Medical Case Reports, 2010
Introduction Guillain-Barré syndrome is an immune-mediated polyneuropathy that is routinely initially treated with either intravenous immunoglobulin or plasmapheresis.
Weimer Louis H, Stevenson Mary L, Bogorad Ilya V   +2 more
doaj   +1 more source