Sabbà C - Search Results

1

Hereditary hemorrhagic teleangiectasia (Rendu-Osler-Weber disease).

Sabbà C, Pasculli G, Cirulli A, Gallitelli M, Virgilio G, Resta F, Guastamacchia E, Palasciano G. Sabbà C, et al. Minerva Cardioangiol. 2002 Jun;50(3):221-38. Minerva Cardioangiol. 2002. PMID: 12107402 Review. English, Italian.

2

Rendu-Osler-Weber disease: experience with 56 patients.

Sabbà C, Pasculli G, Cirulli A, Gallitelli M, Virgilio G, Guastamacchia E, Resta F, Palasciano G. Sabbà C, et al. Ann Ital Med Int. 2002 Jul-Sep;17(3):173-9. Ann Ital Med Int. 2002. PMID: 12402665

3

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.

4

Angiogenesis and hereditary hemorrhagic telangiectasia. Rendu-Osler-Weber disease.

Sabbà C, Cirulli A, Rizzi R, Pasculli G, Gallitelli M, Specchia G, Liso V. Sabbà C, et al. Acta Haematol. 2001;106(4):214-9. doi: 10.1159/000046618. Acta Haematol. 2001. PMID: 11815719 Review.

5

Vascular endothelial growth factor serum levels are elevated in patients with hereditary hemorrhagic telangiectasia.

Cirulli A, Liso A, D'Ovidio F, Mestice A, Pasculli G, Gallitelli M, Rizzi R, Specchia G, Sabbà C. Cirulli A, et al. Among authors: sabba c. Acta Haematol. 2003;110(1):29-32. doi: 10.1159/000072411. Acta Haematol. 2003. PMID: 12975554

6

Brain abscess: a need to screen for pulmonary arteriovenous malformations.

Gallitelli M, Lepore V, Pasculli G, Di Gennaro L, Logroscino G, Carella A, White RI, Sabbà C. Gallitelli M, et al. Among authors: sabba c. Neuroepidemiology. 2005;24(1-2):76-8. doi: 10.1159/000081053. Epub 2004 Sep 24. Neuroepidemiology. 2005. PMID: 15459513

7

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

8

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

9

Pulmonary arteriovenous malformations, hereditary hemorrhagic telangiectasia, and brain abscess.

Gallitelli M, Guastamacchia E, Resta F, Guanti G, Sabbà C. Gallitelli M, et al. Among authors: sabba c. Respiration. 2006;73(4):553-7. doi: 10.1159/000087150. Epub 2005 Jul 21. Respiration. 2006. PMID: 16043953

10

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

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