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

Year Number of Results
1995 1
1996 2
1997 2
1998 2
1999 2
2000 1
2001 2
2002 1
2003 4
2004 1
2005 6
2006 5
2007 3
2008 3
2009 3
2010 2
2011 2
2012 4
2013 4
2014 2
2015 3
2016 4
2017 1
2018 2
2019 4
2020 1
2021 2
2022 0
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62 results
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Page 1
Mitochondrial abnormalities in inclusion-body myositis.
Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C. Oldfors A, et al. Among authors: moslemi ar. Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. doi: 10.1212/01.wnl.0000192127.63013.8d. Neurology. 2006. PMID: 16432145 Review.
An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Pagnamenta AT, Kaiyrzhanov R, Zou Y, Da'as SI, Maroofian R, Donkervoort S, Dominik N, Lauffer M, Ferla MP, Orioli A, Giess A, Tucci A, Beetz C, Sedghi M, Ansari B, Barresi R, Basiri K, Cortese A, Elgar G, Fernandez-Garcia MA, Yip J, Foley AR, Gutowski N, Jungbluth H, Lassche S, Lavin T, Marcelis C, Marks P, Marini-Bettolo C, Medne L, Moslemi AR, Sarkozy A, Reilly MM, Muntoni F, Millan F, Muraresku CC, Need AC, Nemeth AH, Neuhaus SB, Norwood F, O'Donnell M, O'Driscoll M, Rankin J, Yum SW, Zolkipli-Cunningham Z, Brusius I, Wunderlich G; Genomics England Research Consortium, Karakaya M, Wirth B, Fakhro KA, Tajsharghi H, Bönnemann CG, Taylor JC, Houlden H. Pagnamenta AT, et al. Among authors: moslemi ar. Brain. 2021 Mar 3;144(2):584-600. doi: 10.1093/brain/awaa420. Brain. 2021. PMID: 33559681 Free PMC article.
Mitochondrial pathology in inclusion body myositis.
Lindgren U, Roos S, Hedberg Oldfors C, Moslemi AR, Lindberg C, Oldfors A. Lindgren U, et al. Among authors: moslemi ar. Neuromuscul Disord. 2015 Apr;25(4):281-8. doi: 10.1016/j.nmd.2014.12.010. Epub 2015 Jan 6. Neuromuscul Disord. 2015. PMID: 25638290
Prevalence of antibodies to a new histo-blood system: the FORS system.
Jesus C, Hesse C, Rocha C, Osório N, Valado A, Caseiro A, Gabriel A, Svensson L, Moslemi AR, Siba WA, Srour MA, Pereira C, Tomaz J, Teixeira P, Mendes F. Jesus C, et al. Among authors: moslemi ar. Blood Transfus. 2018 Feb;16(2):178-183. doi: 10.2450/2016.0120-16. Epub 2016 Oct 24. Blood Transfus. 2018. PMID: 27893352 Free PMC article.
Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia.
Kariminejad A, Szenker-Ravi E, Lekszas C, Tajsharghi H, Moslemi AR, Naert T, Tran HT, Ahangari F, Rajaei M, Nasseri M, Haaf T, Azad A, Superti-Furga A, Maroofian R, Ghaderi-Sohi S, Najmabadi H, Abbaszadegan MR, Vleminckx K, Nikuei P, Reversade B. Kariminejad A, et al. Among authors: moslemi ar. Am J Hum Genet. 2019 Dec 5;105(6):1294-1301. doi: 10.1016/j.ajhg.2019.10.013. Epub 2019 Nov 21. Am J Hum Genet. 2019. PMID: 31761294 Free PMC article.
62 results