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

Year Number of Results
2003 1
2005 3
2006 4
2007 6
2008 12
2009 11
2010 5
2011 4
2012 14
2013 10
2014 17
2015 14
2016 14
2017 25
2018 13
2019 17
2020 20
2021 24
2022 10
2023 11
2024 3

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203 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: burns j. 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.
Systematic review of exercise for Charcot-Marie-Tooth disease.
Sman AD, Hackett D, Fiatarone Singh M, Fornusek C, Menezes MP, Burns J. Sman AD, et al. Among authors: burns j. J Peripher Nerv Syst. 2015 Dec;20(4):347-62. doi: 10.1111/jns.12116. J Peripher Nerv Syst. 2015. PMID: 26010435 Review.
Inherited Neuropathies.
Carroll AS, Burns J, Nicholson G, Kiernan MC, Vucic S. Carroll AS, et al. Among authors: burns j. Semin Neurol. 2019 Oct;39(5):620-639. doi: 10.1055/s-0039-1693006. Epub 2019 Oct 22. Semin Neurol. 2019. PMID: 31639845 Review.
Interventions for congenital talipes equinovarus (clubfoot).
Bina S, Pacey V, Barnes EH, Burns J, Gray K. Bina S, et al. Among authors: burns j. Cochrane Database Syst Rev. 2020 May 15;5(5):CD008602. doi: 10.1002/14651858.CD008602.pub4. Cochrane Database Syst Rev. 2020. PMID: 32412098 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. 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.
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: burns j. Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323. Brain. 2020. PMID: 33415332 Free PMC article.
Phototheranostics Using Erythrocyte-Based Particles.
Hanley T, Vankayala R, Lee CH, Tang JC, Burns JM, Anvari B. Hanley T, et al. Among authors: burns jm. Biomolecules. 2021 May 13;11(5):729. doi: 10.3390/biom11050729. Biomolecules. 2021. PMID: 34068081 Free PMC article. Review.
Interventions for promoting physical activity in people with neuromuscular disease.
Jones K, Hawke F, Newman J, Miller JA, Burns J, Jakovljevic DG, Gorman G, Turnbull DM, Ramdharry G. Jones K, et al. Among authors: burns j. Cochrane Database Syst Rev. 2021 May 24;5(5):CD013544. doi: 10.1002/14651858.CD013544.pub2. Cochrane Database Syst Rev. 2021. PMID: 34027632 Free PMC article.
203 results