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

Year Number of Results
2006 3
2009 2
2010 1
2011 4
2012 1
2013 4
2014 1
2015 2
2016 1
2017 2
2018 1
2020 2
2021 1
2022 1
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24 results
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Page 1
Papillary thyroid carcinoma in Peutz-Jeghers syndrome.
Triggiani V, Guastamacchia E, Renzulli G, Giagulli VA, Tafaro E, Licchelli B, Resta F, Sabbà C, Bagnulo R, Lastella P, Stella A, Resta N. Triggiani V, et al. Among authors: lastella p. Thyroid. 2011 Nov;21(11):1273-7. doi: 10.1089/thy.2011.0063. Epub 2011 Aug 30. Thyroid. 2011. PMID: 21877933 Review.
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: lastella p. 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
Anticipation in lynch syndrome: where we are where we go.
Bozzao C, Lastella P, Stella A. Bozzao C, et al. Among authors: lastella p. Curr Genomics. 2011 Nov;12(7):451-65. doi: 10.2174/138920211797904070. Curr Genomics. 2011. PMID: 22547953 Free PMC article.
The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein.
Laforgia N, De Cosmo L, Palumbo O, Ranieri C, Sesta M, Capodiferro D, Pantaleo A, Iapicca P, Lastella P, Capozza M, Schettini F, Bukvic N, Bagnulo R, Resta N. Laforgia N, et al. Among authors: lastella p. Genes (Basel). 2020 Dec 18;11(12):1519. doi: 10.3390/genes11121519. Genes (Basel). 2020. PMID: 33353066 Free PMC article.
24 results