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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 2
2021 5
2022 2
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29 results
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Page 1
Characterization of epidemiological distribution and outcome of COVID-19 in patients with hereditary hemorrhagic telangiectasia: a nationwide retrospective multi-centre study during first wave in Italy.
Suppressa P, Pagella F, Lenato GM, Gaetani E, Serio I, Masala MS, Spinozzi G, Lizzio R, Matti E, De Silvestri A, Passali GC, Aguglia M, Crocione C, Sabbà C. Suppressa P, et al. Among authors: lenato gm. Orphanet J Rare Dis. 2021 Sep 8;16(1):378. doi: 10.1186/s13023-021-02000-2. Orphanet J Rare Dis. 2021. PMID: 34496900 Free PMC article.
Safety of reduced or absent antithrombotic therapy after left atrial appendage closure in patients affected by hereditary haemorrhagic telangiectasia and atrial fibrillation.
Pepe M, Suppressa P, Giuliano AF, Nestola PL, Bortone AS, DE Cillis E, Acquaviva T, Forleo C, Moscarelli M, Lenato GM, SabbÀ C. Pepe M, et al. Among authors: lenato gm. Minerva Cardiol Angiol. 2021 Mar 11. doi: 10.23736/S2724-5683.20.05474-2. Online ahead of print. Minerva Cardiol Angiol. 2021. PMID: 33703853
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.
European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT).
Eker OF, Boccardi E, Sure U, Patel MC, Alicante S, Alsafi A, Coote N, Droege F, Dupuis O, Fialla AD, Jones B, Kariholu U, Kjeldsen AD, Lefroy D, Lenato GM, Mager HJ, Manfredi G, Nielsen TH, Pagella F, Post MC, Rennie C, Sabbà C, Suppressa P, Toerring PM, Ugolini S, Buscarini E, Dupuis-Girod S, Shovlin CL. Eker OF, et al. Among authors: lenato gm. Orphanet J Rare Dis. 2020 Jun 29;15(1):165. doi: 10.1186/s13023-020-01386-9. Orphanet J Rare Dis. 2020. PMID: 32600364 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
29 results