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

Year Number of Results
2001 1
2002 4
2003 2
2004 2
2005 1
2006 1
2008 1
2009 2
2010 3
2011 2
2013 1
2014 2
2015 1
2016 3
2017 1
2022 1
2023 1
2024 0

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27 results

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Page 1
Natural history of infantile-onset spinal muscular atrophy.
Kolb SJ, Coffey CS, Yankey JW, Krosschell K, Arnold WD, Rutkove SB, Swoboda KJ, Reyna SP, Sakonju A, Darras BT, Shell R, Kuntz N, Castro D, Parsons J, Connolly AM, Chiriboga CA, McDonald C, Burnette WB, Werner K, Thangarajh M, Shieh PB, Finanger E, Cudkowicz ME, McGovern MM, McNeil DE, Finkel R, Iannaccone ST, Kaye E, Kingsley A, Renusch SR, McGovern VL, Wang X, Zaworski PG, Prior TW, Burghes AHM, Bartlett A, Kissel JT; NeuroNEXT Clinical Trial Network on behalf of the NN101 SMA Biomarker Investigators. Kolb SJ, et al. Among authors: kaye e. Ann Neurol. 2017 Dec;82(6):883-891. doi: 10.1002/ana.25101. Epub 2017 Dec 8. Ann Neurol. 2017. PMID: 29149772 Free PMC article.
Eteplirsen for the treatment of Duchenne muscular dystrophy.
Mendell JR, Rodino-Klapac LR, Sahenk Z, Roush K, Bird L, Lowes LP, Alfano L, Gomez AM, Lewis S, Kota J, Malik V, Shontz K, Walker CM, Flanigan KM, Corridore M, Kean JR, Allen HD, Shilling C, Melia KR, Sazani P, Saoud JB, Kaye EM; Eteplirsen Study Group. Mendell JR, et al. Among authors: kaye em. Ann Neurol. 2013 Nov;74(5):637-47. doi: 10.1002/ana.23982. Epub 2013 Sep 10. Ann Neurol. 2013. PMID: 23907995 Free article. Clinical Trial.
Frontotemporal dementia and pharmacologic interventions.
Kaye ED, Petrovic-Poljak A, Verhoeff NP, Freedman M. Kaye ED, et al. J Neuropsychiatry Clin Neurosci. 2010 Winter;22(1):19-29. doi: 10.1176/jnp.2010.22.1.19. J Neuropsychiatry Clin Neurosci. 2010. PMID: 20160206 Review.
Lysosomal Storage Diseases.
Kaye EM. Kaye EM. Curr Treat Options Neurol. 2001 May;3(3):249-256. doi: 10.1007/s11940-001-0006-9. Curr Treat Options Neurol. 2001. PMID: 11282040
Stakeholder cooperation to overcome challenges in orphan medicine development: the example of Duchenne muscular dystrophy.
Straub V, Balabanov P, Bushby K, Ensini M, Goemans N, De Luca A, Pereda A, Hemmings R, Campion G, Kaye E, Arechavala-Gomeza V, Goyenvalle A, Niks E, Veldhuizen O, Furlong P, Stoyanova-Beninska V, Wood MJ, Johnson A, Mercuri E, Muntoni F, Sepodes B, Haas M, Vroom E, Aartsma-Rus A. Straub V, et al. Among authors: kaye e. Lancet Neurol. 2016 Jul;15(8):882-890. doi: 10.1016/S1474-4422(16)30035-7. Lancet Neurol. 2016. PMID: 27302365 Review.
Does gender parity exist in Fabry disease?
Percy AK, Kaye EM. Percy AK, et al. Among authors: kaye em. Neurology. 2005 Aug 23;65(4):508-9. doi: 10.1212/01.wnl.0000176869.88481.8d. Neurology. 2005. PMID: 16116105 No abstract available.
Diagnosis and management of mitochondrial diseases.
Gillis L, Kaye E. Gillis L, et al. Among authors: kaye e. Pediatr Clin North Am. 2002 Feb;49(1):203-19. doi: 10.1016/s0031-3955(03)00115-9. Pediatr Clin North Am. 2002. PMID: 11826805 Review.
27 results