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American Journal of Human Genetics|April 3, 2012
Rare mutations in XRCC2 increase the risk of breast cancerD J Park, F Lesueur, T Nguyen-Dumont, et al.
JAMA|September 28, 2023
Eplontersen for Hereditary Transthyretin Amyloidosis With PolyneuropathyTeresa Coelho, Wilson Marques, Noel R Dasgupta, et al.
The New England Journal of Medicine|July 5, 2018
Inotersen Treatment for Patients with Hereditary Transthyretin AmyloidosisMerrill D Benson, Márcia Waddington-Cruz, John L Berk, et al.
Muscle & Nerve|February 9, 2026
Dynamics of Nerve Conduction Studies in Patients With Guillain-Barré SyndromeSamuel Arends, Laura de Koning, Judith Drenthen, et al.
Brain : a Journal of Neurology|September 25, 2018
Regional variation of Guillain-Barré syndromeAlex Y Doets, Christine Verboon, Bianca van den Berg, et al.
Brain : a Journal of Neurology|March 17, 2025
Large-scale profiling of antibody reactivity to glycolipids in patients with Guillain-Barré syndromeRobin C M Thomma, Susan K Halstead, Laura C de Koning, et al.
Neurology|August 18, 2022
An International Perspective on Preceding Infections in Guillain-Barré Syndrome: The IGOS-1000 CohortSonja E Leonhard, Annemiek A van der Eijk, Henning Andersen, et al.
Neurology|December 23, 2021
Predicting Outcome in Guillain-Barré Syndrome: International Validation of the Modified Erasmus GBS Outcome ScoreAlex Y Doets, Hester F Lingsma, Christa Walgaard, et al.
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