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

Year Number of Results
2003 1
2005 2
2006 5
2007 2
2008 1
2009 1
2011 1
2012 3
2013 5
2015 1
2017 1
2019 1
2020 1
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23 results
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Page 1
Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia.
Shovlin CL, Millar CM, Droege F, Kjeldsen A, Manfredi G, Suppressa P, Ugolini S, Coote N, Fialla AD, Geisthoff U, Lenato GM, Mager HJ, Pagella F, Post MC, Sabbà C, Sure U, Torring PM, Dupuis-Girod S, Buscarini E; VASCERN-HHT. Shovlin CL, et al. Among authors: lenato gm. Orphanet J Rare Dis. 2019 Aug 28;14(1):210. doi: 10.1186/s13023-019-1179-1. Orphanet J Rare Dis. 2019. PMID: 31462308 Free PMC article.
Hereditary Haemorrhagic Telangiectasia (HHT): genetic and molecular aspects.
Lenato GM, Guanti G. Lenato GM, et al. Curr Pharm Des. 2006;12(10):1173-93. doi: 10.2174/138161206776361291. Curr Pharm Des. 2006. PMID: 16611099 Review.
Hepatic angiodynamic profile in paediatric patients with hereditary haemorrhagic telangiectasia type 1 and type 2.
Giordano P, Francavilla M, Buonamico P, Suppressa P, Lastella P, Sangerardi M, Miniello VL, Scardapane A, Lenato GM, Sabbà C. Giordano P, et al. Among authors: lenato gm. Vasa. 2017 May;46(3):195-202. doi: 10.1024/0301-1526/a000616. Epub 2017 Mar 1. Vasa. 2017. PMID: 28248153
Hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia [corrected].
Scarano V, De Santis D, Suppressa P, Lastella P, Lenato GM, Triggiani V, Sabbà C. Scarano V, et al. Among authors: lenato gm. Case Rep Endocrinol. 2013;2013:465376. doi: 10.1155/2013/465376. Epub 2013 Apr 4. Case Rep Endocrinol. 2013. PMID: 23710379 Free PMC article.
Hereditary hemorrhagic telangiectasia: arteriovenous malformations in children.
Giordano P, Lenato GM, Suppressa P, Lastella P, Dicuonzo F, Chiumarulo L, Sangerardi M, Piccarreta P, Valerio R, Scardapane A, Marano G, Resta N, Quaranta N, Sabbà C. Giordano P, et al. Among authors: lenato gm. J Pediatr. 2013 Jul;163(1):179-86.e1-3. doi: 10.1016/j.jpeds.2013.02.009. Epub 2013 Mar 25. J Pediatr. 2013. PMID: 23535011
Erratum to "hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia".
Scarano V, De Santis D, Suppressa P, Lastella P, Lenato GM, Triggiani V, Sabbà C. Scarano V, et al. Among authors: lenato gm. Case Rep Endocrinol. 2013;2013:520284. doi: 10.1155/2013/520284. Epub 2013 Jul 16. Case Rep Endocrinol. 2013. PMID: 23956891 Free PMC article. No abstract available.
Hereditary haemorrhagic telangiectasia: a rare disease as a model for the study of human atherosclerosis.
Lenato GM, Suppressa P, Giordano P, Guanti G, Guastamacchia E, Triggiani V, Amati L, Resta F, Covelli V, Jirillo E, Sabbà C. Lenato GM, et al. Curr Pharm Des. 2007;13(36):3656-64. doi: 10.2174/138161207783018572. Curr Pharm Des. 2007. PMID: 18220803
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
Resta N, Pierannunzio D, Lenato GM, Stella A, Capocaccia R, Bagnulo R, Lastella P, Susca FC, Bozzao C, Loconte DC, Sabbà C, Urso E, Sala P, Fornasarig M, Grammatico P, Piepoli A, Host C, Turchetti D, Viel A, Memo L, Giunti L, Stigliano V, Varesco L, Bertario L, Genuardi M, Lucci Cordisco E, Tibiletti MG, Di Gregorio C, Andriulli A, Ponz de Leon M; AIFEG. Resta N, et al. Among authors: lenato gm. Dig Liver Dis. 2013 Jul;45(7):606-11. doi: 10.1016/j.dld.2012.12.018. Epub 2013 Feb 15. Dig Liver Dis. 2013. PMID: 23415580
Life expectancy in patients with hereditary haemorrhagic telangiectasia.
Sabbà C, Pasculli G, Suppressa P, D'Ovidio F, Lenato GM, Resta F, Assennato G, Guanti G. Sabbà C, et al. Among authors: lenato gm. QJM. 2006 May;99(5):327-34. doi: 10.1093/qjmed/hcl037. Epub 2006 Apr 4. QJM. 2006. PMID: 16595564
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy).
Piglionica M, Baldassarra SL, Giardina E, Stella A, D'Ovidio FD, Frati P, Lenato GM, Resta N, Dell'Erba A. Piglionica M, et al. Among authors: lenato gm. Forensic Sci Int Genet. 2013 Jan;7(1):e3-4. doi: 10.1016/j.fsigen.2012.08.003. Epub 2012 Sep 7. Forensic Sci Int Genet. 2013. PMID: 22960096
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