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

Year Number of Results
2002 1
2003 1
2004 2
2006 1
2007 1
2008 3
2009 2
2011 3
2012 2
2013 4
2014 1
2015 4
2016 2
2017 1
2018 4
2019 5
2020 1
2021 1
2022 4
2023 5
2024 1

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43 results

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Page 1
Optical coherence tomography angiography findings in Williams-Beuren syndrome.
Nassisi M, Mainetti C, Sperti A, Galmozzi G, Aretti A, Leone G, Nicotra V, Grilli F, Rinaldi B, Natacci F, Bedeschi MF, Viola F. Nassisi M, et al. Among authors: natacci f. Graefes Arch Clin Exp Ophthalmol. 2024 Apr;262(4):1131-1140. doi: 10.1007/s00417-023-06323-7. Epub 2023 Nov 30. Graefes Arch Clin Exp Ophthalmol. 2024. PMID: 38032380
The Contribution of Oxidative Stress to NF1-Altered Tumors.
Kuhn E, Natacci F, Corbo M, Pisani L, Ferrero S, Bulfamante G, Gambini D. Kuhn E, et al. Among authors: natacci f. Antioxidants (Basel). 2023 Aug 4;12(8):1557. doi: 10.3390/antiox12081557. Antioxidants (Basel). 2023. PMID: 37627552 Free PMC article. Review.
Ocular features in Williams-Beuren syndrome: a review of the literature.
Nassisi M, Mainetti C, Aretti A, Sperti A, Nicotra V, Rinaldi B, Natacci F, Bedeschi MF, Viola F. Nassisi M, et al. Among authors: natacci f. Curr Opin Ophthalmol. 2023 Nov 1;34(6):514-521. doi: 10.1097/ICU.0000000000000990. Epub 2023 Aug 17. Curr Opin Ophthalmol. 2023. PMID: 37589562 Review.
New insights into the molecular basis of spinal neurofibromatosis type 1.
Bettinaglio P, Mangano E, Tritto V, Bordoni R, Paterra R, Borghi A, Volontè M, Battaglia C, Saletti V, Cesaretti C, Natacci F, Melone MAB, Eoli M, Riva P. Bettinaglio P, et al. Among authors: natacci f. Eur J Hum Genet. 2023 Aug;31(8):931-938. doi: 10.1038/s41431-023-01377-x. Epub 2023 May 22. Eur J Hum Genet. 2023. PMID: 37217626 Free article.
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.
Paterra R, Bettinaglio P, Borghi A, Mangano E, Tritto V, Cesaretti C, Schettino C, Bordoni R, Santoro C, Avignone S, Moscatelli M, Melone MAB, Saletti V, Piluso G, Natacci F, Riva P, Eoli M. Paterra R, et al. Among authors: natacci f. Cancers (Basel). 2022 Dec 22;15(1):59. doi: 10.3390/cancers15010059. Cancers (Basel). 2022. PMID: 36612057 Free PMC article.
Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome.
Bestetti I, Crippa M, Sironi A, Tumiatti F, Masciadri M, Smeland MF, Naik S, Murch O, Bonati MT, Spano A, Cattaneo E, Mariani M, Gotta F, Crosti F, Cavalli P, Pantaleoni C, Natacci F, Bedeschi MF, Milani D, Maitz S, Selicorni A, Spaccini L, Peron A, Russo S, Larizza L, Low K, Finelli P. Bestetti I, et al. Among authors: natacci f. Int J Mol Sci. 2022 May 25;23(11):5912. doi: 10.3390/ijms23115912. Int J Mol Sci. 2022. PMID: 35682590 Free PMC article.
43 results