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Genetic Testing and Molecular Biomarkers|January 12, 2010
Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descentChai Saechao, Yadira Valles-Ayoub, Saghi Esfandiarifard, et al.Schizophrenia Research|December 1, 2009
Tailoring the definition of the clinical schizophrenia phenotype in linkage studiesVerena Krause, Olga Krastoshevsky, Michael J Coleman, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 26, 2014
VIP-expressing dendritic cells protect against spontaneous autoimmune peripheral polyneuropathyMehmet E Yalvac, William David Arnold, Syed-Rehan A Hussain, et al.Cell|July 9, 2024
A non-canonical role for a small nucleolar RNA in ribosome biogenesis and senescenceYujing Cheng, Siwen Wang, He Zhang, et al.Neurology|February 1, 1997
Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletionT W Prior, C Bartolo, A C Papp, et al.Journal of Clinical Apheresis|January 1, 1985
Plasma exchange and prednisone in acute inflammatory polyradiculoneuropathy: a controlled randomized trialJ R Mendell, J T Kissel, M S Kennedy, et al.Muscle & Nerve|November 1, 1988
Clinical investigation in Duchenne muscular dystrophy: penicillamine and vitamin EG M Fenichel, M H Brooke, R C Griggs, et al.BMC Proceedings|December 19, 2009
Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysisSu-Wei Chang, Seung Hoan Choi, Ke Li, et al.Genes & Development|July 21, 2018
Mutations in microRNA processing genes in Wilms tumors derepress the <i>IGF2</i> regulator <i>PLAG1</i>Kenneth S Chen, Emily K Stroup, Albert Budhipramono, et al.Neurology. Clinical Practice|August 4, 2025
Limb-Girdle Muscular Dystrophy Scientific Workshop: A Multistakeholder Discussion Focused on Charting the Path Forward for Drug DevelopmentMatthew P Wicklund, Lindsay N Alfano, Nicholas E Johnson, et al.Pageof 89