Cirulli A - 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. Among authors: cirulli a. 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. Among authors: cirulli a. Ann Ital Med Int. 2002 Jul-Sep;17(3):173-9. Ann Ital Med Int. 2002. PMID: 12402665

3

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. Among authors: cirulli a. Acta Haematol. 2001;106(4):214-9. doi: 10.1159/000046618. Acta Haematol. 2001. PMID: 11815719 Review.

4

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. Acta Haematol. 2003;110(1):29-32. doi: 10.1159/000072411. Acta Haematol. 2003. PMID: 12975554

5

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: cirulli a. Clin Genet. 2003 Jun;63(6):536-40. doi: 10.1034/j.1399-0004.2003.00081.x. Clin Genet. 2003. PMID: 12786761

6

Evidence of small-bowel involvement in hereditary hemorrhagic telangiectasia: a capsule-endoscopic study.

Ingrosso M, Sabbà C, Pisani A, Principi M, Gallitelli M, Cirulli A, Francavilla A. Ingrosso M, et al. Among authors: cirulli a. Endoscopy. 2004 Dec;36(12):1074-9. doi: 10.1055/s-2004-826045. Endoscopy. 2004. PMID: 15578297

7

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: cirulli a. Radiol Med. 2005 Jan-Feb;109(1-2):125-38. Radiol Med. 2005. PMID: 15729193 English, Italian.

8

Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement.

Ianora AA, Memeo M, Sabba C, Cirulli A, Rotondo A, Angelelli G. Ianora AA, et al. Among authors: cirulli a. Radiology. 2004 Jan;230(1):250-9. doi: 10.1148/radiol.2301021745. Epub 2003 Nov 26. Radiology. 2004. PMID: 14645886

9

Patients with Hereditary Hemorrhagic Telangectasia (HHT) exhibit a deficit of polymorphonuclear cell and monocyte oxidative burst and phagocytosis: a possible correlation with altered adaptive immune responsiveness in HHT.

Cirulli A, Loria MP, Dambra P, Di Serio F, Ventura MT, Amati L, Jirillo E, Sabbà C. Cirulli A, et al. Curr Pharm Des. 2006;12(10):1209-15. doi: 10.2174/138161206776361336. Curr Pharm Des. 2006. PMID: 16611102

10

Takayasu arteritis: a cohort of Italian patients and recent pathogenetic and therapeutic advances.

Dammacco F, Cirulli A, Simeone A, Leone P, Pulli R, Angiletta D, Rubini G, Di Palo A, Vacca A, Dammacco R. Dammacco F, et al. Among authors: cirulli a. Clin Exp Med. 2021 Feb;21(1):49-62. doi: 10.1007/s10238-020-00668-7. Epub 2020 Oct 7. Clin Exp Med. 2021. PMID: 33026580 Free PMC article.

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