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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.

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Neurofibromatosis type 1 and melanoma of the iris arising from a dysplastic nevus: A rare yet casual association?

Alessio G, Guerriero S, Albano V, Piscitelli D, Falcone V, Lastella P, Resta N, Stella A. Alessio G, et al. Among authors: lastella p. Eur J Ophthalmol. 2021 May;31(3):NP45-NP49. doi: 10.1177/1120672120906999. Epub 2020 Feb 16. Eur J Ophthalmol. 2021. PMID: 32064917

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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: lastella p. Case Rep Endocrinol. 2013;2013:465376. doi: 10.1155/2013/465376. Epub 2013 Apr 4. Case Rep Endocrinol. 2013. PMID: 23710379 Free PMC article.

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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

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Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1.

Stella A, Lastella P, Loconte DC, Bukvic N, Varvara D, Patruno M, Bagnulo R, Lovaglio R, Bartolomeo N, Serio G, Resta N. Stella A, et al. Among authors: lastella p. Genes (Basel). 2018 Apr 17;9(4):216. doi: 10.3390/genes9040216. Genes (Basel). 2018. PMID: 29673180 Free PMC article.

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Familial adenomatous polyposis small bowel surveillance: could indicators for video-capsule endoscopy be ascertained?

Papagni S, Rizzi S, Principi M, Albano F, Contaldo A, Iannone A, Losurdo G, Genco E, Lastella P, Ierardi E, DI Leo A. Papagni S, et al. Among authors: lastella p. Minerva Gastroenterol Dietol. 2016 Sep;62(3):272-3. Minerva Gastroenterol Dietol. 2016. PMID: 27404265 No abstract available.

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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.

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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.

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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: lastella p. Vasa. 2017 May;46(3):195-202. doi: 10.1024/0301-1526/a000616. Epub 2017 Mar 1. Vasa. 2017. PMID: 28248153

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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: lastella p. 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.

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