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Human Molecular Genetics|June 10, 2010
Identification of a new NEMO/TRAF6 interface affected in incontinentia pigmenti pathologyJérémie Gautheron, Alessandra Pescatore, Francesca Fusco, et al.
Case Reports in Gastroenterology|September 6, 2012
Acute inflammatory bowel disease complicating chronic alcoholism and mimicking carcinoid syndromePiercarlo Ballo, Pietro Dattolo, Giuseppe Mangialavori, et al.
International Reviews of Immunology|August 14, 2015
EDA-ID and IP, two faces of the same coin: how the same IKBKG/NEMO mutation affecting the NF-κB pathway can cause immunodeficiency and/or inflammationFrancesca Fusco, Alessandra Pescatore, Matilde Immacolata Conte, et al.
Orphanet Journal of Rare Diseases|June 26, 2014
Incontinentia pigmenti: report on data from 2000 to 2013Francesca Fusco, Mariateresa Paciolla, Matilde Immacolata Conte, et al.
Human Molecular Genetics|August 31, 2007
Identification of TRAF6-dependent NEMO polyubiquitination sites through analysis of a new NEMO mutation causing incontinentia pigmentiHélène Sebban-Benin, Alessandra Pescatore, Francesca Fusco, et al.
Pediatrics|August 11, 2017
Unusual Father-to-Daughter Transmission of Incontinentia Pigmenti Due to Mosaicism in IP MalesFrancesca Fusco, Matilde Immacolata Conte, Andrea Diociaiuti, et al.
Oxford Medical Case Reports|July 7, 2018
Giant isolated intracardiac thrombus presenting as acute heart failure secondary to right ventricular outflow tract obstruction in a patient with renal carcinomaPiercarlo Ballo, Veronica Fibbi, Massimo Granelli, et al.
Clinical Immunology (Orlando, Fla.)|August 27, 2015
B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligandGiuliana Giardino, Emilia Cirillo, Vera Gallo, et al.
Applied Neuropsychology. Child|June 9, 2016
Cognitive-behavioural phenotype in a group of girls from 1.2 to 12 years old with the Incontinentia Pigmenti syndrome: Recommendations for clinical managementMaria Rosa Pizzamiglio, Laura Piccardi, Filippo Bianchini, et al.
Human Molecular Genetics|July 2, 2004
Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activationFrancesca Fusco, Tiziana Bardaro, Giorgia Fimiani, et al.
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