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

Year Number of Results
1977 1
1981 1
1985 1
1989 1
1992 1
1993 1
1995 1
1997 4
1998 4
1999 4
2000 4
2001 2
2002 7
2003 4
2004 2
2005 4
2006 3
2007 4
2008 5
2009 5
2010 7
2011 5
2012 4
2013 12
2014 8
2015 9
2016 9
2017 7
2018 2
2019 8
2020 5
2021 1
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Similar articles for PMID: 10699117

125 results
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Page 1
Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome.
Messiaen L, Yao S, Brems H, Callens T, Sathienkijkanchai A, Denayer E, Spencer E, Arn P, Babovic-Vuksanovic D, Bay C, Bobele G, Cohen BH, Escobar L, Eunpu D, Grebe T, Greenstein R, Hachen R, Irons M, Kronn D, Lemire E, Leppig K, Lim C, McDonald M, Narayanan V, Pearn A, Pedersen R, Powell B, Shapiro LR, Skidmore D, Tegay D, Thiese H, Zackai EH, Vijzelaar R, Taniguchi K, Ayada T, Okamoto F, Yoshimura A, Parret A, Korf B, Legius E. Messiaen L, et al. JAMA. 2009 Nov 18;302(19):2111-8. doi: 10.1001/jama.2009.1663. JAMA. 2009. PMID: 19920235
[Phenotypic and genetic features in neurofibromatosis type 1 in children].
Duat Rodríguez A, Martos Moreno GÁ, Martín Santo-Domingo Y, Hernández Martín A, Espejo-Saavedra Roca JM, Ruiz-Falcó Rojas ML, Argente J. Duat Rodríguez A, et al. An Pediatr (Barc). 2015 Sep;83(3):173-82. doi: 10.1016/j.anpedi.2014.10.010. Epub 2014 Dec 23. An Pediatr (Barc). 2015. PMID: 25541118 Free article. Spanish.
Comprehensive RNA Analysis of the NF1 Gene in Classically Affected NF1 Affected Individuals Meeting NIH Criteria has High Sensitivity and Mutation Negative Testing is Reassuring in Isolated Cases With Pigmentary Features Only.
Evans DG, Bowers N, Burkitt-Wright E, Miles E, Garg S, Scott-Kitching V, Penman-Splitt M, Dobbie A, Howard E, Ealing J, Vassalo G, Wallace AJ, Newman W; Northern UK NF1 Research Network, Huson SM. Evans DG, et al. EBioMedicine. 2016 May;7:212-20. doi: 10.1016/j.ebiom.2016.04.005. Epub 2016 Apr 13. EBioMedicine. 2016. PMID: 27322474 Free PMC article.
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