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Page 1
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: pasculli g. Neuroepidemiology. 2005;24(1-2):76-8. doi: 10.1159/000081053. Epub 2004 Sep 24. Neuroepidemiology. 2005. PMID: 15459513
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: pasculli g. Ann Ital Med Int. 2002 Jul-Sep;17(3):173-9. Ann Ital Med Int. 2002. PMID: 12402665
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: pasculli g. Minerva Cardioangiol. 2002 Jun;50(3):221-38. Minerva Cardioangiol. 2002. PMID: 12107402 Review. English, Italian.
Emergencies in hereditary haemorrhagic telangiectasia.
Gallitelli M, Pasculli G, Fiore T, Carella A, Sabbà C. Gallitelli M, et al. Among authors: pasculli g. QJM. 2006 Jan;99(1):15-22. doi: 10.1093/qjmed/hci148. Epub 2005 Dec 8. QJM. 2006. PMID: 16339212
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: pasculli g. Curr Pharm Des. 2006;12(10):1217-20. doi: 10.2174/138161206776361219. Curr Pharm Des. 2006. PMID: 16611103 Review.
30 results