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Neurology. Genetics|June 14, 2019
Novel mutation in <i>TNPO3</i> causes congenital limb-girdle myopathy with slow progressionAnna Vihola, Johanna Palmio, Olof Danielsson, et al.The Journal of Clinical Investigation|June 15, 2023
Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2EChengcheng Li, Jackson Wilborn, Sara Pittman, et al.Plos One|April 16, 2011
Solid-phase microextraction and the human fecal VOC metabolomeEmma Dixon, Cynthia Clubb, Sara Pittman, et al.Science Translational Medicine|November 27, 2024
Seeding-competent TDP-43 persists in human patient and mouse muscleEileen M Lynch, Sara Pittman, Jil Daw, et al.Biorxiv : the Preprint Server for Biology|April 15, 2024
Seeding competent TDP-43 persists in human patient and mouse muscleEileen M Lynch, Sara Pittman, Jil Daw, et al.Human Molecular Genetics|March 15, 2023
Connective tissue presentation in two families expands the phenotypic spectrum of PYROXD1 disordersFrances J Evesson, Gregory Dziaduch, Samantha J Bryen, et al.Molecular Neurodegeneration|April 13, 2022
VCP suppresses proteopathic seeding in neuronsJiang Zhu, Sara Pittman, Dhruva Dhavale, et al.Pageof 1