Steven S. Scherer, MD PhD
Affiliations: | Neurology | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Peripheral nerveWebsite:
http://www.med.upenn.edu/ins/faculty/scherer.htmGoogle:
"Steven Scherer"Mean distance: 14.48 (cluster 11) | S | N | B | C | P |
Cross-listing: Neuropathology Tree
Parents
Sign in to add mentor| Stephen S. Easter Jr. | grad student | 1983-1985 | University of Michigan |
| John Kamholz | post-doc | 1989-1991 | Penn (Cell Biology Tree) |
Children
Sign in to add trainee| Edgardo J. Arroyo | grad student | 1992-1997 | Penn |
| Jennifer L. Orthmann-Murphy | grad student | 2007 | Penn |
| Chih H. King | grad student | 2012 | Penn |
| Kleopas A Kleopa | post-doc | 2001-2004 | Penn |
| Jerome Devaux | post-doc | 2003-2006 | Penn |
| Sabrina W. Yum | post-doc | 2002-2007 | Penn |
| Wiliam W. Motley | post-doc | 2015-2016 | Penn |
| M. Laura Feltri | research scientist |
BETA: Related publications
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Publications
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| Kosmanopoulos G, Donohue JK, Hoke M, et al. (2024) TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations. Brain : a Journal of Neurology |
| Rebelo AP, Abad C, Dohrn MF, et al. (2024) SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Brain : a Journal of Neurology |
| Baldwin A, Copeland J, Azage M, et al. (2024) Disparities in Genetic Testing for Neurologic Disorders. Neurology. 102: e209161 |
| Scherer SS, Svaren J. (2024) Peripheral Nervous System (PNS) Myelin Diseases. Cold Spring Harbor Perspectives in Biology |
| Rebelo AP, Abad C, Dohrn MF, et al. (2023) Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights. Biorxiv : the Preprint Server For Biology |
| Dratch L, Azage M, Baldwin A, et al. (2023) Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts. Journal of Neurology |
| Record CJ, Skorupinska M, Laura M, et al. (2023) Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants. Brain : a Journal of Neurology |
| Rehbein T, Wu TT, Treidler S, et al. (2023) Neuropathy due to bi-allelic SH3TC2 variants: Genotype-phenotype correlation and natural history. Brain : a Journal of Neurology |
| Fridman V, Sillau S, Bockhorst J, et al. (2022) Disease Progression in CMT related to MPZ Mutations: A Longitudinal Study. Annals of Neurology |
| McLean JW, Wilson JA, Tian T, et al. (2022) Disruption of endosomal sorting in Schwann cells leads to defective myelination and endosomal abnormalities observed in Charcot-Marie-Tooth disease. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |