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Brain Injury|June 13, 2018
Is balance performance reduced after mild traumatic brain injury?: Interim analysis from chronic effects of neurotrauma consortium (CENC) multi-centre studyWilliam C Walker, Kayla J Nowak, Kimbra Kenney, et al.
Genomics|May 20, 1999
Bestrophin gene mutations in patients with Best vitelliform macular dystrophyG M Caldwell, L E Kakuk, I B Griesinger, et al.
Brain : a Journal of Neurology|October 28, 2025
IgA autoantibodies demonstrate a novel mechanism of MuSK myasthenia gravis pathologyGianvito Masi, Kangzhi Chen, Alexandra C Bayer, et al.
Scientific Reports|August 2, 2018
L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathyAdriana M Messineo, Charlotte Gineste, Tamar E Sztal, et al.
Neurology|April 19, 2023
Addressing Outcome Measure Variability in Myasthenia Gravis Clinical TrialsJeffrey T Guptill, Michael Benatar, Volkan Granit, et al.
JCI Insight|April 25, 2023
MOGAD patient autoantibodies induce complement, phagocytosis, and cellular cytotoxicitySoumya S Yandamuri, Beata Filipek, Abeer H Obaid, et al.
Tissue Antigens|February 7, 2014
IL-10 promoter polymorphisms influence susceptibility to aGvHD and are associated with proportions of CD4+FoxP3+ lymphocytes in blood after hematopoietic stem cell transplantationE Jaskula, A Lange, D Dlubek, et al.
European Journal of Human Genetics : EJHG|November 18, 2025
Enhancing the detection of familial hypercholesterolaemia in general practice: A model for supporting genetic cascade testing in the communityJing Pang, Wendy Barnett, Jane Purdie, et al.
Muscle & Nerve|May 7, 2021
Telemedicine visits in myasthenia gravis: Expert guidance and the Myasthenia Gravis Core Exam (MG-CE)Amanda C Guidon, Srikanth Muppidi, Richard J Nowak, et al.
Stem Cell Research|June 21, 2022
Generation of two isogenic induced pluripotent stem cell lines from a 1-month-old nemaline myopathy patient harbouring a homozygous recessive c.121C > T (p.Arg39Ter) variant in the ACTA1 geneIsabella S Suleski, Robert Smith, Christina Vo, et al.
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