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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1984 2
1986 3
1987 1
1988 1
1989 1
1990 3
1991 1
1992 2
1993 2
1994 3
1995 1
1996 2
1997 3
1998 2
1999 19
2000 6
2001 6
2002 7
2003 5
2004 5
2005 6
2006 9
2007 10
2008 12
2009 12
2010 8
2011 13
2012 12
2013 10
2014 16
2015 21
2016 6
2017 19
2018 19
2019 16
2020 16
2021 11
2022 15
2023 20
2024 5

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302 results

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Page 1
Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease.
Yiu EM, Bray P, Baets J, Baker SK, Barisic N, de Valle K, Estilow T, Farrar MA, Finkel RS, Haberlová J, Kennedy RA, Moroni I, Nicholson GA, Ramchandren S, Reilly MM, Rose K, Shy ME, Siskind CE, Yum SW, Menezes MP, Ryan MM, Burns J. Yiu EM, et al. Among authors: shy me. J Neurol Neurosurg Psychiatry. 2022 May;93(5):530-538. doi: 10.1136/jnnp-2021-328483. Epub 2022 Feb 9. J Neurol Neurosurg Psychiatry. 2022. PMID: 35140138 Review.
Hereditary neuropathy.
Pisciotta C, Shy ME. Pisciotta C, et al. Among authors: shy me. Handb Clin Neurol. 2023;195:609-617. doi: 10.1016/B978-0-323-98818-6.00009-1. Handb Clin Neurol. 2023. PMID: 37562889 Review.
Neuropathy.
Pisciotta C, Shy ME. Pisciotta C, et al. Among authors: shy me. Handb Clin Neurol. 2018;148:653-665. doi: 10.1016/B978-0-444-64076-5.00042-9. Handb Clin Neurol. 2018. PMID: 29478606 Review.
The integrated stress response contributes to tRNA synthetase-associated peripheral neuropathy.
Spaulding EL, Hines TJ, Bais P, Tadenev ALD, Schneider R, Jewett D, Pattavina B, Pratt SL, Morelli KH, Stum MG, Hill DP, Gobet C, Pipis M, Reilly MM, Jennings MJ, Horvath R, Bai Y, Shy ME, Alvarez-Castelao B, Schuman EM, Bogdanik LP, Storkebaum E, Burgess RW. Spaulding EL, et al. Among authors: shy me. Science. 2021 Sep 3;373(6559):1156-1161. doi: 10.1126/science.abb3414. Epub 2021 Sep 1. Science. 2021. PMID: 34516839 Free PMC article.
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Among authors: shy me. Nat Genet. 2020 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
Phase 2 Trial of Rituximab in Acetylcholine Receptor Antibody-Positive Generalized Myasthenia Gravis: The BeatMG Study.
Nowak RJ, Coffey CS, Goldstein JM, Dimachkie MM, Benatar M, Kissel JT, Wolfe GI, Burns TM, Freimer ML, Nations S, Granit V, Smith AG, Richman DP, Ciafaloni E, Al-Lozi MT, Sams LA, Quan D, Ubogu E, Pearson B, Sharma A, Yankey JW, Uribe L, Shy M, Amato AA, Conwit R, O'Connor KC, Hafler DA, Cudkowicz ME, Barohn RJ; NeuroNEXT NN103 BeatMG Study Team. Nowak RJ, et al. Among authors: shy m. Neurology. 2022 Jan 25;98(4):e376-e389. doi: 10.1212/WNL.0000000000013121. Neurology. 2022. PMID: 34857535 Free PMC article.
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
Pipis M, Feely SME, Polke JM, Skorupinska M, Perez L, Shy RR, Laura M, Morrow JM, Moroni I, Pisciotta C, Taroni F, Vujovic D, Lloyd TE, Acsadi G, Yum SW, Lewis RA, Finkel RS, Herrmann DN, Day JW, Li J, Saporta M, Sadjadi R, Walk D, Burns J, Muntoni F, Ramchandren S, Horvath R, Johnson NE, Züchner S, Pareyson D, Scherer SS, Rossor AM, Shy ME, Reilly MM; Inherited Neuropathies Consortium - Rare Disease Clinical Research Network (INC-RDCRN). Pipis M, et al. Among authors: shy me. Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323. Brain. 2020. PMID: 33415332 Free PMC article.
Peripheral neuropathy in mitochondrial disease.
Horvath R, Medina J, Reilly MM, Shy ME, Zuchner S. Horvath R, et al. Among authors: shy me. Handb Clin Neurol. 2023;194:99-116. doi: 10.1016/B978-0-12-821751-1.00014-2. Handb Clin Neurol. 2023. PMID: 36813324 Review.
Genetics of neuropathies.
Siskind CE, Shy ME. Siskind CE, et al. Among authors: shy me. Semin Neurol. 2011 Nov;31(5):494-505. doi: 10.1055/s-0031-1299788. Epub 2012 Jan 21. Semin Neurol. 2011. PMID: 22266887 Review.
Advances in diagnosis and management of distal sensory polyneuropathies.
Silsby M, Feldman EL, Dortch RD, Roth A, Haroutounian S, Rajabally YA, Vucic S, Shy ME, Oaklander AL, Simon NG. Silsby M, et al. Among authors: shy me. J Neurol Neurosurg Psychiatry. 2023 Dec;94(12):1025-1039. doi: 10.1136/jnnp-2021-328489. Epub 2023 Mar 30. J Neurol Neurosurg Psychiatry. 2023. PMID: 36997315 Review.
302 results