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

Year Number of Results
2002 1
2004 1
2008 6
2009 3
2010 6
2011 7
2012 16
2013 9
2014 10
2015 8
2016 8
2017 1
2018 1
2020 0
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68 results
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Page 1
Immune-mediated pathology in Duchenne muscular dystrophy.
Rosenberg AS, Puig M, Nagaraju K, Hoffman EP, Villalta SA, Rao VA, Wakefield LM, Woodcock J. Rosenberg AS, et al. Sci Transl Med. 2015 Aug 5;7(299):299rv4. doi: 10.1126/scitranslmed.aaa7322. Sci Transl Med. 2015. PMID: 26246170 Free PMC article. Review.
Congenital Titinopathy: Comprehensive characterization and pathogenic insights.
Oates EC, Jones KJ, Donkervoort S, Charlton A, Brammah S, Smith JE 3rd, Ware JS, Yau KS, Swanson LC, Whiffin N, Peduto AJ, Bournazos A, Waddell LB, Farrar MA, Sampaio HA, Teoh HL, Lamont PJ, Mowat D, Fitzsimons RB, Corbett AJ, Ryan MM, O'Grady GL, Sandaradura SA, Ghaoui R, Joshi H, Marshall JL, Nolan MA, Kaur S, Punetha J, Töpf A, Harris E, Bakshi M, Genetti CA, Marttila M, Werlauff U, Streichenberger N, Pestronk A, Mazanti I, Pinner JR, Vuillerot C, Grosmann C, Camacho A, Mohassel P, Leach ME, Foley AR, Bharucha-Goebel D, Collins J, Connolly AM, Gilbreath HR, Iannaccone ST, Castro D, Cummings BB, Webster RI, Lazaro L, Vissing J, Coppens S, Deconinck N, Luk HM, Thomas NH, Foulds NC, Illingworth MA, Ellard S, McLean CA, Phadke R, Ravenscroft G, Witting N, Hackman P, Richard I, Cooper ST, Kamsteeg EJ, Hoffman EP, Bushby K, Straub V, Udd B, Ferreiro A, North KN, Clarke NF, Lek M, Beggs AH, Bönnemann CG, MacArthur DG, Granzier H, Davis MR, Laing NG. Oates EC, et al. Ann Neurol. 2018 Jun;83(6):1105-1124. doi: 10.1002/ana.25241. Ann Neurol. 2018. PMID: 29691892 Free PMC article.
Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects.
Punetha J, Kesari A, Hoffman EP, Gos M, Kamińska A, Kostera-Pruszczyk A, Hausmanowa-Petrusewicz I, Hu Y, Zou Y, Bönnemann CG, JȨdrzejowska M. Punetha J, et al. Muscle Nerve. 2017 Feb;55(2):277-281. doi: 10.1002/mus.25232. Epub 2016 Nov 30. Muscle Nerve. 2017. PMID: 27348394 Free PMC article.
Genome-wide identification of significant aberrations in cancer genome.
Yuan X, Yu G, Hou X, Shih IeM, Clarke R, Zhang J, Hoffman EP, Wang RR, Zhang Z, Wang Y. Yuan X, et al. BMC Genomics. 2012 Jul 27;13:342. doi: 10.1186/1471-2164-13-342. BMC Genomics. 2012. PMID: 22839576 Free PMC article.
Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegia.
Willkomm L, Heredia R, Hoffmann K, Wang H, Voit T, Hoffman EP, Cirak S. Willkomm L, et al. J Hum Genet. 2016 Jun;61(6):571-3. doi: 10.1038/jhg.2016.6. Epub 2016 Feb 18. J Hum Genet. 2016. PMID: 26888483
TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular Dystrophy.
Fiorillo AA, Heier CR, Novak JS, Tully CB, Brown KJ, Uaesoontrachoon K, Vila MC, Ngheim PP, Bello L, Kornegay JN, Angelini C, Partridge TA, Nagaraju K, Hoffman EP. Fiorillo AA, et al. Cell Rep. 2015 Sep 8;12(10):1678-90. doi: 10.1016/j.celrep.2015.07.066. Epub 2015 Aug 28. Cell Rep. 2015. PMID: 26321630 Free PMC article.
Genomics, intellectual disability, and autism.
Mefford HC, Batshaw ML, Hoffman EP. Mefford HC, et al. N Engl J Med. 2012 Feb 23;366(8):733-43. doi: 10.1056/NEJMra1114194. N Engl J Med. 2012. PMID: 22356326 Free PMC article. Review. No abstract available.
Laminopathies disrupt epigenomic developmental programs and cell fate.
Perovanovic J, Dell'Orso S, Gnochi VF, Jaiswal JK, Sartorelli V, Vigouroux C, Mamchaoui K, Mouly V, Bonne G, Hoffman EP. Perovanovic J, et al. Sci Transl Med. 2016 Apr 20;8(335):335ra58. doi: 10.1126/scitranslmed.aad4991. Sci Transl Med. 2016. PMID: 27099177 Free PMC article.
Novel approaches to corticosteroid treatment in Duchenne muscular dystrophy.
Hoffman EP, Reeves E, Damsker J, Nagaraju K, McCall JM, Connor EM, Bushby K. Hoffman EP, et al. Phys Med Rehabil Clin N Am. 2012 Nov;23(4):821-8. doi: 10.1016/j.pmr.2012.08.003. Phys Med Rehabil Clin N Am. 2012. PMID: 23137739 Free PMC article. Review.
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