Giorgia Cordisco
Overview
Explore the profile of Giorgia Cordisco including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
7
Citations
140
Followers
0
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Recent Articles
1.
dApolito M, Santacroce R, Vazquez D, Cordisco G, Fantini C, DAndrea G, et al.
J Allergy Clin Immunol
. 2024 Jun;
154(3):698-706.
PMID: 38823490
Background: In the recent years, there was an important improvement in the understanding of the pathogenesis of hereditary angioedema (HAE). Notwithstanding, in a large portion of patients with unknown mutation...
2.
dApolito M, Santoro F, Santacroce R, Cordisco G, Ragnatela I, DArienzo G, et al.
Genes (Basel)
. 2023 Feb;
14(2).
PMID: 36833354
Background: Brugada syndrome (BrS) is an inherited primary channelopathy syndrome associated to sudden cardiac death. Overall, variants have been identified in eighteen genes encoding for ion channel subunits and seven...
3.
Bova M, Suffritti C, Bafunno V, Loffredo S, Cordisco G, Del Giacco S, et al.
Allergy
. 2019 Dec;
75(6):1394-1403.
PMID: 31860755
Background: Hereditary angioedema (HAE) comprises HAE with C1-inhibitor deficiency (C1-INH-HAE) and HAE with normal C1-INH activity (nl-C1-INH-HAE), due to mutations in factor XII (FXII-HAE), plasminogen (PLG-HAE), angiopoietin 1 (ANGPT1-HAE), kininogen...
4.
Bottigliero D, Monaco I, Santacroce R, Casavecchia G, Correale M, Guastafierro F, et al.
J Interv Card Electrophysiol
. 2019 Aug;
56(2):171-172.
PMID: 31418098
No abstract available.
5.
dApolito M, Santacroce R, Colia A, Cordisco G, Maffione A, Margaglione M
Clin Exp Allergy
. 2019 Jan;
49(5):626-635.
PMID: 30689269
Background: Different mutations of the angiopoietin-1 gene (ANGPT1) have been associated with the occurrence of hereditary angioedema (HAE). Objective: The purpose of the study is to clarify whether the ANGPT1...
6.
Monaco I, Santacroce R, Casavecchia G, Correale M, Bottigliero D, Cordisco G, et al.
J Electrocardiol
. 2019 Jan;
53:40-43.
PMID: 30611920
Here we report the identification of two novel mutations in a previously asymptomatic young man who suffered an out-of-hospital sudden cardiac arrest. During following evaluation, diagnosis of early stage dilated...
7.
Bafunno V, Firinu D, dApolito M, Cordisco G, Loffredo S, Leccese A, et al.
J Allergy Clin Immunol
. 2017 Jun;
141(3):1009-1017.
PMID: 28601681
Background: Hereditary angioedema (HAE) is a rare genetic disease usually caused by mutation in the C1 inhibitor or the coagulation Factor XII gene. However, in a series of patients with...