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

Year Number of Results
1985 2
1986 7
1987 4
1988 3
1989 7
1990 3
1991 2
1992 9
1993 6
1994 4
1995 4
1996 2
1997 3
1998 1
1999 5
2000 5
2001 4
2002 2
2003 2
2004 1
2005 2
2006 4
2007 5
2008 1
2009 2
2010 4
2011 5
2012 8
2013 8
2014 2
2015 3
2016 2
2018 2
2019 1
2020 1
2021 1
2022 3
2024 0

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119 results

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Page 1
Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation.
Legius E, Messiaen L, Wolkenstein P, Pancza P, Avery RA, Berman Y, Blakeley J, Babovic-Vuksanovic D, Cunha KS, Ferner R, Fisher MJ, Friedman JM, Gutmann DH, Kehrer-Sawatzki H, Korf BR, Mautner VF, Peltonen S, Rauen KA, Riccardi V, Schorry E, Stemmer-Rachamimov A, Stevenson DA, Tadini G, Ullrich NJ, Viskochil D, Wimmer K, Yohay K; International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC); Huson SM, Evans DG, Plotkin SR. Legius E, et al. Among authors: huson sm. Genet Med. 2021 Aug;23(8):1506-1513. doi: 10.1038/s41436-021-01170-5. Epub 2021 May 19. Genet Med. 2021. PMID: 34012067 Free PMC article.
Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation.
Plotkin SR, Messiaen L, Legius E, Pancza P, Avery RA, Blakeley JO, Babovic-Vuksanovic D, Ferner R, Fisher MJ, Friedman JM, Giovannini M, Gutmann DH, Hanemann CO, Kalamarides M, Kehrer-Sawatzki H, Korf BR, Mautner VF, MacCollin M, Papi L, Rauen KA, Riccardi V, Schorry E, Smith MJ, Stemmer-Rachamimov A, Stevenson DA, Ullrich NJ, Viskochil D, Wimmer K, Yohay K; International Consensus Group on Neurofibromatosis Diagnostic Criteria (I-NF-DC); Huson SM, Wolkenstein P, Evans DG. Plotkin SR, et al. Among authors: huson sm. Genet Med. 2022 Sep;24(9):1967-1977. doi: 10.1016/j.gim.2022.05.007. Epub 2022 Jun 9. Genet Med. 2022. PMID: 35674741 Free article.
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. Among authors: huson sm. 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.
The neurofibromatoses. An overview.
Ruggieri M, Huson SM. Ruggieri M, et al. Among authors: huson sm. Ital J Neurol Sci. 1999 Apr;20(2):89-108. doi: 10.1007/s100720050017. Ital J Neurol Sci. 1999. PMID: 10933430 Review.
The different forms of neurofibromatosis.
Huson SM. Huson SM. Br Med J (Clin Res Ed). 1987 May 2;294(6580):1113-4. doi: 10.1136/bmj.294.6580.1113. Br Med J (Clin Res Ed). 1987. PMID: 3107717 Free PMC article. No abstract available.
Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome.
Huson SM, Staab T, Pereira M, Ward H, Paredes R, Evans DG, Baumhoer D, O'Sullivan J, Cheesman E, Schindler D, Meyer S. Huson SM, et al. Fam Cancer. 2022 Jan;21(1):85-90. doi: 10.1007/s10689-020-00221-1. Epub 2020 Nov 21. Fam Cancer. 2022. PMID: 33219493 Free PMC article.
What level of care for the neurofibromatoses?
Huson SM. Huson SM. Lancet. 1999 Apr 3;353(9159):1114-6. doi: 10.1016/S0140-6736(98)00155-X. Lancet. 1999. PMID: 10209971 Review. No abstract available.
119 results