User profiles for David Piccoli

David A Piccoli

Children's Hospital of Philadelphia, University of Pennsylvania
Verified email at email.chop.edu
Cited by 16120

Diet in the pathogenesis and treatment of inflammatory bowel diseases

…, L Albenberg, C Compher, R Baldassano, D Piccoli… - Gastroenterology, 2015 - Elsevier
Some of the most common symptoms of the inflammatory bowel diseases (IBD, which include
ulcerative colitis and Crohn’s disease) are abdominal pain, diarrhea, and weight loss. It is …

Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality

…, KM Emerick, AE Chudley, C Booth, DA Piccoli… - Circulation, 2004 - Am Heart Assoc
Background— Alagille syndrome (AGS) is a dominantly inherited multisystem disorder
involving the liver, heart, eyes, face, and skeleton, caused by mutations in Jagged1. Intracranial …

Inflammatory bowel disease in pediatric and adolescent patients

RN Baldassano, DA Piccoli - Gastroenterology Clinics of North America, 1999 - Elsevier
Once considered rare in pedatric practice, chronic inflammatory bowel disease (IBD) is now
being recognized with increasing frequency in children of all ages. In fact, 25% to 30% of all …

Common variants at five new loci associated with early-onset inflammatory bowel disease

…, J Essers, R Grand, M Stephens, A Levine, D Piccoli… - Nature …, 2009 - nature.com
The inflammatory bowel diseases (IBD) Crohn's disease and ulcerative colitis are common
causes of morbidity in children and young adults in the western world. Here we report the …

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

…, T Costa, MEM Pierpont, EB Rand, DA Piccoli… - Nature …, 1997 - nature.com
Alagille syndrome is an autosomal dominant disorder characterized by abnormal development
of liver, heart, skeleton, eye, face and, less frequently, kidney. Analyses of many patients …

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

…, BL Pike, K Okajima, ID Krantz, A Genin, DA Piccoli… - Nature …, 1997 - nature.com
Alagille syndrome (AGS) is an autosomal-dominant disorder characterized by intrahepatic
cholestasis and abnormalities of heart, eye and vertebrae, as well as a characteristic facial …

[PDF][PDF] NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway

…, PA Sanchez-Lara, A Pai, ID Krantz, DA Piccoli… - The American Journal of …, 2006 - cell.com
Alagille syndrome (AGS) is caused by mutations in the gene for the Notch signaling pathway
ligand Jagged1 (JAG1), which are found in 94% of patients. To identify the cause of …

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis

…, E Goldmuntz, ID Krantz, NB Spinner, DA Piccoli - Hepatology, 1999 - journals.lww.com
We have studied 92 patients with Alagille syndrome (AGS) to determine the frequency of
clinical manifestations and to correlate the clinical findings with outcome. Liver biopsy …

[PDF][PDF] Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

…, S Guthery, L Denson, D Piccoli… - The American Journal of …, 2009 - cell.com
Previous genome-wide association (GWA) studies typically focus on single-locus analysis,
which may not have the power to detect the majority of genuinely associated loci. Here, we …

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

…, R Grundmeier, P Mamula, G Tomer, DA Piccoli… - Nature …, 2008 - nature.com
Inflammatory bowel disease (IBD) is a common inflammatory disorder with complex etiology
that involves both genetic and environmental triggers, including but not limited to defects in …