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Results by year

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

Year Number of Results
1949 2
1960 1
1961 1
1965 2
1967 1
1969 2
1970 2
1975 2
1978 1
1987 1
1989 3
1993 1
1996 1
1997 1
1998 1
1999 2
2000 1
2001 2
2002 3
2003 9
2004 4
2005 5
2006 7
2007 7
2008 9
2009 13
2010 9
2011 9
2012 8
2013 9
2014 9
2015 8
2016 12
2017 7
2018 8
2019 13
2020 16
2021 14
2022 20
2023 15
2024 7

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229 results

Results by year

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Page 1
Spinal muscular atrophy.
Mercuri E, Sumner CJ, Muntoni F, Darras BT, Finkel RS. Mercuri E, et al. Among authors: sumner cj. Nat Rev Dis Primers. 2022 Aug 4;8(1):52. doi: 10.1038/s41572-022-00380-8. Nat Rev Dis Primers. 2022. PMID: 35927425 Review.
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. Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323. Brain. 2020. PMID: 33415332 Free PMC article.
Approaches to Greening Radiology.
Sumner C, Ikuta I, Garg T, Martin JG, Mansoori B, Chalian M, Englander BS, Chertoff J, Woolen S, Caplin D, Sneider MB, Desouches SL, Chan TL, Kadom N. Sumner C, et al. Acad Radiol. 2023 Mar;30(3):528-535. doi: 10.1016/j.acra.2022.08.013. Epub 2022 Sep 13. Acad Radiol. 2023. PMID: 36114076 Review.
Psychedelics, With a Focus on Psilocybin: Issues for the Clinician.
Garakani A, Alexander JL, Sumner CR, Pine JH, Gross LS, Raison CL, Aaronson ST, Baron DA. Garakani A, et al. Among authors: sumner cr. J Psychiatr Pract. 2023 Sep 1;29(5):345-353. doi: 10.1097/PRA.0000000000000729. J Psychiatr Pract. 2023. PMID: 37678363 Review.
Neuropsychiatric aspects of concussion.
Radhakrishnan R, Garakani A, Gross LS, Goin MK, Pine J, Slaby AE, Sumner CR, Baron DA. Radhakrishnan R, et al. Among authors: sumner cr. Lancet Psychiatry. 2016 Dec;3(12):1166-1175. doi: 10.1016/S2215-0366(16)30266-8. Lancet Psychiatry. 2016. PMID: 27889010 Review.
Autosomal Dominant TRPV4 Disorders.
McCray BA, Schindler A, Hoover-Fong JE, Sumner CJ. McCray BA, et al. Among authors: sumner cj. 2014 May 15 [updated 2020 Sep 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2014 May 15 [updated 2020 Sep 17]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 24830047 Free Books & Documents. Review.
Peripheral Neuropathy: No Longer the Land of Therapeutic Nihilism.
Polydefkis M, Sumner CJ. Polydefkis M, et al. Among authors: sumner cj. Neurotherapeutics. 2021 Oct;18(4):2153-2155. doi: 10.1007/s13311-021-01177-5. Epub 2022 Jan 6. Neurotherapeutics. 2021. PMID: 34993888 Free PMC article. No abstract available.
WHAT MAKES HUMAN HEARING SPECIAL?
Sumner CJ, Bergevin C, Oxenham AJ, Shera CA. Sumner CJ, et al. Front Young Minds. 2022;10:708921. doi: 10.3389/frym.2022.708921. Epub 2022 May 31. Front Young Minds. 2022. PMID: 37465203 Free PMC article.
229 results