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Disparities in Genetic Testing for Neurologic Disorders.
Baldwin A, Copeland J, Azage M, Dratch L, Johnson K, Paul RA, Amado DA, Baer M, Deik A, Elman LB, Guo M, Hamedani AG, Irwin DJ, Lasker A, Orthmann-Murphy J, Quinn CC, Tropea TF, Scherer SS, Shinohara RT, Hamilton RH, Ellis CA. Baldwin A, et al. Among authors: scherer ss. Neurology. 2024 Mar 26;102(6):e209161. doi: 10.1212/WNL.0000000000209161. Epub 2024 Mar 6. Neurology. 2024. PMID: 38447117
Gap junctions couple astrocytes and oligodendrocytes.
Orthmann-Murphy JL, Abrams CK, Scherer SS. Orthmann-Murphy JL, et al. Among authors: scherer ss. J Mol Neurosci. 2008 May;35(1):101-16. doi: 10.1007/s12031-007-9027-5. J Mol Neurosci. 2008. PMID: 18236012 Free PMC article. Review.
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations.
Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS, Pareyson D. Orthmann-Murphy JL, et al. Among authors: scherer ss. Brain. 2009 Feb;132(Pt 2):426-38. doi: 10.1093/brain/awn328. Epub 2008 Dec 4. Brain. 2009. PMID: 19056803 Free PMC article.
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies.
Burnor E, Yang L, Zhou H, Patterson KR, Quinn C, Reilly MM, Rossor AM, Scherer SS, Lancaster E. Burnor E, et al. Among authors: scherer ss. Neurology. 2018 Jan 2;90(1):e31-e38. doi: 10.1212/WNL.0000000000004773. Epub 2017 Nov 29. Neurology. 2018. PMID: 29187518 Free PMC article.
POLG mutations presenting as Charcot-Marie-Tooth disease.
Phillips J, Courel S, Rebelo AP, Bis-Brewer DM, Bardakjian T, Dankwa L, Hamedani AG, Züchner S, Scherer SS. Phillips J, et al. Among authors: scherer ss. J Peripher Nerv Syst. 2019 Jun;24(2):213-218. doi: 10.1111/jns.12313. Epub 2019 Apr 10. J Peripher Nerv Syst. 2019. PMID: 30843307 Free PMC article.
250 results