Sabbà C - Search Results

1

Efficacy of Lomitapide in the Treatment of Familial Homozygous Hypercholesterolemia: Results of a Real-World Clinical Experience in Italy.

D'Erasmo L, Cefalù AB, Noto D, Giammanco A, Averna M, Pintus P, Medde P, Vigna GB, Sirtori C, Calabresi L, Pavanello C, Bucci M, Sabbà C, Suppressa P, Natale F, Calabrò P, Sampietro T, Bigazzi F, Sbrana F, Bonomo K, Sileo F, Arca M. D'Erasmo L, et al. Among authors: sabba c. Adv Ther. 2017 May;34(5):1200-1210. doi: 10.1007/s12325-017-0531-x. Epub 2017 Apr 21. Adv Ther. 2017. PMID: 28432645

2

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

3

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

4

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.

5

Low dose intravenous bevacizumab for the treatment of anaemia in hereditary haemorrhagic telangiectasia.

Suppressa P, Liso A, Sabbà C. Suppressa P, et al. Among authors: sabba c. Br J Haematol. 2011 Feb;152(4):365. doi: 10.1111/j.1365-2141.2010.08481.x. Epub 2010 Dec 1. Br J Haematol. 2011. PMID: 21265821 Free article. No abstract available.

6

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

7

Subclinical hypothyroidism and cognitive dysfunction in the elderly.

Resta F, Triggiani V, Barile G, Benigno M, Suppressa P, Giagulli VA, Guastamacchia E, Sabbà C. Resta F, et al. Among authors: sabba c. Endocr Metab Immune Disord Drug Targets. 2012 Sep;12(3):260-7. doi: 10.2174/187153012802002875. Endocr Metab Immune Disord Drug Targets. 2012. PMID: 22385117

8

A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study.

Pierucci P, Lenato GM, Suppressa P, Lastella P, Triggiani V, Valerio R, Comelli M, Salvante D, Stella A, Resta N, Logroscino G, Resta F, Sabbà C. Pierucci P, et al. Among authors: sabba c. Orphanet J Rare Dis. 2012 Jun 7;7:33. doi: 10.1186/1750-1172-7-33. Orphanet J Rare Dis. 2012. PMID: 22676497 Free PMC article.

9

Hereditary hemorrhagic telangiectasia: arteriovenous malformations in children.

Giordano P, Lenato GM, Suppressa P, Lastella P, Dicuonzo F, Chiumarulo L, Sangerardi M, Piccarreta P, Valerio R, Scardapane A, Marano G, Resta N, Quaranta N, Sabbà C. Giordano P, et al. Among authors: sabba c. J Pediatr. 2013 Jul;163(1):179-86.e1-3. doi: 10.1016/j.jpeds.2013.02.009. Epub 2013 Mar 25. J Pediatr. 2013. PMID: 23535011

10

Diode laser treatment and clinical management of multiple oral lesions in patients with hereditary haemorrhagic telangiectasia.

Favia G, Tempesta A, Limongelli L, Suppressa P, Sabbà C, Maiorano E. Favia G, et al. Among authors: sabba c. Br J Oral Maxillofac Surg. 2016 May;54(4):379-83. doi: 10.1016/j.bjoms.2015.08.260. Epub 2015 Sep 8. Br J Oral Maxillofac Surg. 2016. PMID: 26360009

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