Suppressa P - Search Results

1

Cardiovascular risk in rare diseases: a prognostic stratification model in a cohort of sarcoidosis patients.

Rizzi L, Coppola C, Cocco V, Sabbà C, Suppressa P. Rizzi L, et al. Among authors: suppressa p. Intern Emerg Med. 2023 Aug;18(5):1437-1444. doi: 10.1007/s11739-023-03314-8. Epub 2023 May 23. Intern Emerg Med. 2023. PMID: 37219757 Free PMC article.

2

Platelet Count Does Not Predict Bleeding in Cirrhotic Patients: Results from the PRO-LIVER Study.

Basili S, Raparelli V, Napoleone L, Talerico G, Corazza GR, Perticone F, Sacerdoti D, Andriulli A, Licata A, Pietrangelo A, Picardi A, Raimondo G, Violi F; PRO-LIVER Collaborators. Basili S, et al. Am J Gastroenterol. 2018 Mar;113(3):368-375. doi: 10.1038/ajg.2017.457. Epub 2017 Dec 19. Am J Gastroenterol. 2018. PMID: 29257146

3

Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study.

Tromp TR, Hartgers ML, Hovingh GK, Vallejo-Vaz AJ, Ray KK, Soran H, Freiberger T, Bertolini S, Harada-Shiba M, Blom DJ, Raal FJ, Cuchel M; Homozygous Familial Hypercholesterolaemia International Clinical Collaborators. Tromp TR, et al. Lancet. 2022 Feb 19;399(10326):719-728. doi: 10.1016/S0140-6736(21)02001-8. Epub 2022 Jan 28. Lancet. 2022. PMID: 35101175 Free PMC article.

4

Asymptomatic microhematuria: an indication of hereditary hemorrhagic telangiectasia?

Di Gennaro L, Ramunni A, Suppressa P, Guastamacchia E, Resta F, Sabbà C. Di Gennaro L, et al. Among authors: suppressa p. J Urol. 2005 Jan;173(1):106-9. doi: 10.1097/01.ju.0000146601.49061.a4. J Urol. 2005. PMID: 15592044

5

Pasculli G, Resta F, Guastamacchia E, Di Gennaro L, Suppressa P, Sabbà C. Pasculli G, et al. Among authors: suppressa p. Qual Life Res. 2004 Dec;13(10):1715-23. doi: 10.1007/s11136-004-7865-y. Qual Life Res. 2004. PMID: 15651542

6

Capillaroscopy of the dorsal skin of the hands in hereditary hemorrhagic telangiectasia.

Pasculli G, Quaranta D, Lenato GM, Suppressa P, Lastella P, Guanti G, Sabbà C. Pasculli G, et al. Among authors: suppressa p. QJM. 2005 Oct;98(10):757-63. doi: 10.1093/qjmed/hci115. Epub 2005 Aug 26. QJM. 2005. PMID: 16126740

7

DHPLC-based mutation analysis of ENG and ALK-1 genes in HHT Italian population.

Lenato GM, Lastella P, Di Giacomo MC, Resta N, Suppressa P, Pasculli G, Sabbà C, Guanti G. Lenato GM, et al. Among authors: suppressa p. Hum Mutat. 2006 Feb;27(2):213-4. doi: 10.1002/humu.9400. Hum Mutat. 2006. PMID: 16429404

8

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: suppressa p. QJM. 2006 May;99(5):327-34. doi: 10.1093/qjmed/hcl037. Epub 2006 Apr 4. QJM. 2006. PMID: 16595564

9

Involvement of the transforming growth factor beta in the pathogenesis of hereditary hemorrhagic telangiectasia.

Jirillo E, Amati L, Suppressa P, Cirimele D, Guastamacchia E, Covelli V, Tafaro E, Sabbà C. Jirillo E, et al. Among authors: suppressa p. Curr Pharm Des. 2006;12(10):1195-200. doi: 10.2174/138161206776361228. Curr Pharm Des. 2006. PMID: 16611100 Review.

10

HHT: a rare disease with a broad spectrum of clinical aspects.

Sabbà C, Gallitelli M, Pasculli G, Suppressa P, Resta F, Tafaro GE. Sabbà C, et al. Among authors: suppressa p. Curr Pharm Des. 2006;12(10):1217-20. doi: 10.2174/138161206776361219. Curr Pharm Des. 2006. PMID: 16611103 Review.

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