Gallitelli M - Search Results

1

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

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: gallitelli m. Ann Ital Med Int. 2002 Jul-Sep;17(3):173-9. Ann Ital Med Int. 2002. PMID: 12402665

3

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: gallitelli m. Minerva Cardioangiol. 2002 Jun;50(3):221-38. Minerva Cardioangiol. 2002. PMID: 12107402 Review. English, Italian.

4

Emergencies in hereditary haemorrhagic telangiectasia.

Gallitelli M, Pasculli G, Fiore T, Carella A, Sabbà C. Gallitelli M, et al. QJM. 2006 Jan;99(1):15-22. doi: 10.1093/qjmed/hci148. Epub 2005 Dec 8. QJM. 2006. PMID: 16339212

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: gallitelli m. 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. Neuroepidemiology. 2005;24(1-2):76-8. doi: 10.1159/000081053. Epub 2004 Sep 24. Neuroepidemiology. 2005. PMID: 15459513

7

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: gallitelli m. Acta Haematol. 2001;106(4):214-9. doi: 10.1159/000046618. Acta Haematol. 2001. PMID: 11815719 Review.

8

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

9

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: gallitelli m. Endoscopy. 2004 Dec;36(12):1074-9. doi: 10.1055/s-2004-826045. Endoscopy. 2004. PMID: 15578297

10

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

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

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