Lucia Perroni
Overview
Explore the profile of Lucia Perroni including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
430
Followers
0
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Recent Articles
1.
Piccione M, Consiglio V, Di Fiore A, Grasso M, Cecconi M, Perroni L, et al.
J Genet
. 2011 Jun;
90(1):119-23.
PMID: 21677396
No abstract available.
2.
Passerini L, Di Nunzio S, Gregori S, Gambineri E, Cecconi M, Seidel M, et al.
Eur J Immunol
. 2011 Mar;
41(4):1120-31.
PMID: 21400500
Mutations of forkhead box p3 (FOXP3), the master gene for naturally occurring regulatory T cells (nTregs), are responsible for the impaired function of nTregs, resulting in an autoimmune disease known...
3.
Cocchella A, Malacarne M, Forzano F, Marciano C, Pierluigi M, Perroni L, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2010 Jun;
153B(7):1342-6.
PMID: 20552675
Current literature provides more than 30 patients with interstitial deletions in chromosome 2q31q33. Only a few of them were studied using high-resolution methods. Among these, two patients had presented with...
4.
Di Maria E, Cammarata S, Parodi M, Borghi R, Benussi L, Galli M, et al.
J Alzheimers Dis
. 2010 Feb;
19(3):909-14.
PMID: 20157246
Mild cognitive impairment is often considered a transitional condition prodromal to Alzheimer's disease. The dissection of genetic risk factors predisposing to mild cognitive impairment is paramount to assess the individual...
5.
Grasso M, Cecconi M, Boni S, Forzano F, Barbaresi M, Memo L, et al.
Mol Cell Probes
. 2009 Oct;
24(2):107-9.
PMID: 19836446
Most common inherited form of intellectual disability, fragile X syndrome is associated to an expansion of greater than 200 CGG repeats in the 5' untranslated region of the FMR1 gene...
6.
Di Nunzio S, Cecconi M, Passerini L, McMurchy A, Baron U, Turbachova I, et al.
Blood
. 2009 Sep;
114(19):4138-41.
PMID: 19738030
Forkhead box P3 (FOXP3) is constitutively expressed by CD4(+)CD25(hi) regulatory T cells (nTregs). Mutations of FOXP3 cause a severe autoimmune syndrome known as immune dysregulation polyendocrinopathy enteropathy X-linked, in which...
7.
Cecconi M, Forzano F, Garavelli L, Pantaleoni C, Grasso M, Bricarelli F, et al.
Am J Med Genet A
. 2008 Nov;
146A(23):3095-9.
PMID: 19006215
No abstract available.
8.
Gambineri E, Perroni L, Passerini L, Bianchi L, Doglioni C, Meschi F, et al.
J Allergy Clin Immunol
. 2008 Oct;
122(6):1105-1112.e1.
PMID: 18951619
Background: Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is an autoimmune genetic disorder caused by mutation of the forkhead box protein 3 gene (FOXP3), a key regulator of immune tolerance....
9.
Zhan H, Sinclair J, Adams S, Cale C, Murch S, Perroni L, et al.
Pediatrics
. 2008 Mar;
121(4):e998-1002.
PMID: 18316354
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome is a rare X-linked disorder that usually presents in early childhood with immune enteropathy, diabetes mellitus, and other autoimmune complications. The disease is caused...
10.
Bacchetta R, Passerini L, Gambineri E, Dai M, Allan S, Perroni L, et al.
J Clin Invest
. 2006 Jun;
116(6):1713-22.
PMID: 16741580
The autoimmune disease immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) is caused by mutations in the forkhead box protein P3 (FOXP3) gene. In the mouse model of FOXP3 deficiency, the lack...