G Pasculli
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Explore the profile of G Pasculli including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
129
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Recent Articles
1.
Sabba C, Pasculli G, Lenato G, Suppressa P, Lastella P, Memeo M, et al.
J Thromb Haemost
. 2007 Mar;
5(6):1149-57.
PMID: 17388964
Background: Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder characterized by epistaxis, mucocutaneous telangiectases and visceral arteriovenous malformations (AVMs), particularly in the brain (CAVMs), lungs (PAVMs), liver (HAVMs) and gastrointestinal...
2.
Pasculli G, Sallustio G, Sabba C
Curr Pharm Des
. 2006 Apr;
12(10):1249-51.
PMID: 16611107
In the last years, the understanding of HHT has greatly progressed. The two genes for most on cromosomes 9 and 12 have been discovered and the existence of a third...
3.
Sabba C, Gallitelli M, Pasculli G, Suppressa P, Resta F, Tafaro G
Curr Pharm Des
. 2006 Apr;
12(10):1217-20.
PMID: 16611103
HHT is an autosomal dominant disease characterised by diffuse muco-cutaneous and visceral telangiectases in potentially all organs. Mutations in two different genes identify HHT type 1 and HHT type 2:...
4.
Sabba C, Pasculli G, Suppressa P, DOvidio F, Lenato G, Resta F, et al.
QJM
. 2006 Apr;
99(5):327-34.
PMID: 16595564
Background: There are few data on life expectancy in patients with hereditary haemorrhagic telangiectasia (HHT), a disorder with life-threatening complications. Methods: Seventy HHT patients provided data on age and age...
5.
Gallitelli M, Pasculli G, Fiore T, Carella A, Sabba C
QJM
. 2005 Dec;
99(1):15-22.
PMID: 16339212
Background: Hereditary haemorrhagic telangiectasia (HHT) is a systemic autosomal dominant vascular disease. Although the clinical picture is that of a chronic disabling disease, vascular malformations can suddenly lead to life-threatening...
6.
Pasculli G, Quaranta D, Lenato G, Suppressa P, Lastella P, Guanti G, et al.
QJM
. 2005 Aug;
98(10):757-63.
PMID: 16126740
Background: Cutaneous telangiectases are manifestations of hereditary hemorrhagic telangiectasia (HHT), a dominantly inherited disorder. Telangiectases have been studied by skin biopsy, and recently by nailfold capillaroscopy. Aim: To confirm the...
7.
Sabba C, Pasculli G, Cirulli A, Gallitelli M, Virgilio G, Resta F, et al.
Minerva Cardioangiol
. 2002 Jul;
50(3):221-38.
PMID: 12107402
Rendu-Osler-Weber disease, or hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant disorder with incomplete penetrance, characterized by vascular anomalies which may virtually develop in many organs. The prevalence varies and...
8.
Sabba C, Cirulli A, Rizzi R, Pasculli G, Gallitelli M, Specchia G, et al.
Acta Haematol
. 2002 Jan;
106(4):214-9.
PMID: 11815719
To date much of the recent work on pathological angiogenesis has focused on inflammatory diseases, diabetes and cancer in particular. Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease provides an example of...