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Neurology|February 9, 2021
Funding the Educational Mission in NeurologyDavid M Greer, Jeremy Moeller, Diego R Torres, et al.Neurology|January 9, 2013
Association between performance on Neurology In-Training and Certification ExaminationsDorthea Juul, Frederick G Flynn, Laurie Gutmann, et al.Scientific Reports|March 2, 2021
White matter microstructure relates to motor outcomes in myotonic dystrophy type 1 independently of disease duration and genetic burdenTimothy R Koscik, Ellen van der Plas, Laurie Gutmann, et al.Neurology. Genetics|August 28, 2020
Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1Jacob N Miller, Ellen van der Plas, Mark Hamilton, et al.JAMA Neurology|August 21, 2013
Amyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2Sirinan Tazen, Karla Figueroa, Justin Y Kwan, et al.Annals of Neurology|April 5, 2019
Schwann cell transcript biomarkers for hereditary neuropathy skin biopsiesJohn Svaren, John J Moran, Xingyao Wu, et al.Brain Research. Molecular Brain Research|May 15, 2002
Fatty acid synthase expression during peripheral nervous system myelinationJérôme Salles, Françoise Sargueil, Anja Knoll-Gellida, et al.Annals of the New York Academy of Sciences|November 1, 2017
The Absence of Myelin P0 Protein Produces a Novel Molecular Phenotype in Schwann CellDaniela Maria Menichella, Wenbo Xu, Huiyuan Jiang, et al.Frontiers in Neurology|July 19, 2021
Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1Jacob N Miller, Alison Kruger, David J Moser, et al.Journal of Neurointerventional Surgery|October 15, 2013
Admission neutrophil-lymphocyte ratio predicts 90 day outcome after endovascular stroke therapySteven D Brooks, Chauncey Spears, Christopher Cummings, et al.Pageof 9