Sabbà C - Search Results

1

Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation.

Lastella P, Patruno M, Forte G, Montanaro A, Di Gregorio C, Sabbà C, Suppressa P, Piepoli A, Panza A, Andriulli A, Resta N, Stella A. Lastella P, et al. Among authors: sabba c. Fam Cancer. 2011 Jun;10(2):285-95. doi: 10.1007/s10689-011-9419-0. Fam Cancer. 2011. PMID: 21286823

2

Endoglin gene mutations and polymorphisms in Italian patients with hereditary haemorrhagic telangiectasia.

Lastella P, Sabbà C, Lenato GM, Resta N, Lattanzi W, Gallitelli M, Cirulli A, Guanti G. Lastella P, et al. Among authors: sabba c. Clin Genet. 2003 Jun;63(6):536-40. doi: 10.1034/j.1399-0004.2003.00081.x. Clin Genet. 2003. PMID: 12786761

3

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: sabba c. J Urol. 2005 Jan;173(1):106-9. doi: 10.1097/01.ju.0000146601.49061.a4. J Urol. 2005. PMID: 15592044

4

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

5

Hereditary haemorrhagic telangiectasia: study of hepatic vascular alterations with multi-detector row helical CT and reconstruction programs.

Memeo M, Stabile Ianora AA, Scardapane A, Suppressa P, Cirulli A, Sabbà C, Rotondo A, Angelelli G. Memeo M, et al. Among authors: sabba c. Radiol Med. 2005 Jan-Feb;109(1-2):125-38. Radiol Med. 2005. PMID: 15729193 English, Italian.

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

9

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. Curr Pharm Des. 2006;12(10):1217-20. doi: 10.2174/138161206776361219. Curr Pharm Des. 2006. PMID: 16611103 Review.

10

Screening for children from families with Rendu-Osler-Weber disease: from geneticist to clinician.

Giordano P, Nigro A, Lenato GM, Guanti G, Suppressa P, Lastella P, DE Mattia D, Sabbà C. Giordano P, et al. Among authors: sabba c. J Thromb Haemost. 2006 Jun;4(6):1237-45. doi: 10.1111/j.1538-7836.2006.01934.x. J Thromb Haemost. 2006. PMID: 16706966 Free article.

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