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Protein-Losing Enteropathy in Patients With Congenital Heart Disease

Journal of the American College of Cardiology, 2017-06, Vol.69 (24), p.2929-2937

2017

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Diet in the Pathogenesis and Treatment of Inflammatory Bowel Diseases

Gastroenterology (New York, N.Y. 1943), 2015-05, Vol.148 (6), p.1087-1106

2015

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Reply: The Need to Define Treatment Goals for Protein-Losing Enteropathy in Fontan Care and Research

Journal of the American College of Cardiology, 2017-11, Vol.70 (20), p.2603-2603

2017

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Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification

Human mutation, 2019-12, Vol.40 (12), p.2197-2220

2019

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Intrahepatic dynamic contrast MR lymphangiography: initial experience with a new technique for the assessment of liver lymphatics

European radiology, 2019-10, Vol.29 (10), p.5190-5196

2019

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Autoimmune Pancreatitis in Children: Characteristic Features, Diagnosis, and Management

The American journal of gastroenterology, 2017-10, Vol.112 (10), p.1604-1611

2017

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NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

American journal of human genetics, 2006-07, Vol.79 (1), p.169-173

2006

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Soil physicochemical and biological properties in soybean areas under no-till Systems in the Brazilian Cerrado

The Science of the total environment, 2023-03, Vol.862, p.160674-160674, Article 160674

2023

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Evaluating the biocontrol potential of Canadian strain Bacillus velezensis 1B-23 via its surfactin production at various pHs and temperatures

BMC biotechnology, 2021-04, Vol.21 (1), p.31-31, Article 31

2021

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Dynamic Contrast Magnetic Resonance Lymphangiography Localizes Lymphatic Leak to the Duodenum in Protein‐Losing Enteropathy

Journal of pediatric gastroenterology and nutrition, 2022-01, Vol.74 (1), p.38-45

2022

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Severe Eosinophilic Gastroenteritis in a Crohn's Disease Patient Treated With Infliximab and Adalimumab

The American journal of gastroenterology, 2016-03, Vol.111 (3), p.437-438

2016

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Bone geometry and microarchitecture deficits in children with Alagille syndrome

Bone (New York, N.Y.), 2020-12, Vol.141, p.115576-115576, Article 115576

2020

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NOTCH2 mutations in Alagille syndrome

Journal of medical genetics, 2012-02, Vol.49 (2), p.138-144

2012

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Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease

Inflammatory bowel diseases, 2016-10, Vol.22 (10), p.2425-2431

2016

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Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes

American journal of medical genetics. Part A, 2021-03, Vol.185 (3), p.719-731

2021

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Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results

Genetics in medicine, 2021-02, Vol.23 (2), p.323-330

2021

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Immune Response to Influenza Vaccine in Pediatric Patients With Inflammatory Bowel Disease

Clinical gastroenterology and hepatology, 2007-07, Vol.5 (7), p.851-856

2007

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Protein‐elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

Human mutation, 2020-05, Vol.41 (5), p.973-982

2020

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Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study

Hepatology communications, 2020-03, Vol.4 (3), p.387-398

2020

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Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE

Journal of pediatric gastroenterology and nutrition, 2018-08, Vol.67 (2), p.232-236

2018

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Medical Management of Alagille Syndrome

Journal of pediatric gastroenterology and nutrition, 2010-06, Vol.50 (6), p.580-586

2010

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Vascular anomalies in alagille syndrome: A significant cause of morbidity and mortality

Circulation (New York, N.Y.), 2004-03, Vol.109 (11), p.1354-1358

2004

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Moyamoya Syndrome Associated with Alagille Syndrome: Outcome after Surgical Revascularization

The Journal of pediatrics, 2015-02, Vol.166 (2), p.470-473

2015

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Chromosome 10q23 Deletion Syndrome: An Overlap of Bannayan-Riley-Ruvalcaba Syndrome and Juvenile Polyposis Syndrome

Journal of paediatrics and child health, 2016-08, Vol.52 (8), p.852-852

2016

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Protein-Losing Enteropathy in Patients With Congenital Heart Disease

Diet in the Pathogenesis and Treatment of Inflammatory Bowel Diseases

Reply: The Need to Define Treatment Goals for Protein-Losing Enteropathy in Fontan Care and Research

Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification

Intrahepatic dynamic contrast MR lymphangiography: initial experience with a new technique for the assessment of liver lymphatics

Autoimmune Pancreatitis in Children: Characteristic Features, Diagnosis, and Management

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Soil physicochemical and biological properties in soybean areas under no-till Systems in the Brazilian Cerrado

Evaluating the biocontrol potential of Canadian strain Bacillus velezensis 1B-23 via its surfactin production at various pHs and temperatures

Dynamic Contrast Magnetic Resonance Lymphangiography Localizes Lymphatic Leak to the Duodenum in Protein‐Losing Enteropathy

Severe Eosinophilic Gastroenteritis in a Crohn's Disease Patient Treated With Infliximab and Adalimumab

Bone geometry and microarchitecture deficits in children with Alagille syndrome

NOTCH2 mutations in Alagille syndrome

Vedolizumab Therapy in Severe Pediatric Inflammatory Bowel Disease

Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes

Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results

Immune Response to Influenza Vaccine in Pediatric Patients With Inflammatory Bowel Disease

Protein‐elongating mutations in MYH11 are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease

Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study

Recommendations for Diagnosis and Management of Autoimmune Pancreatitis in Childhood: Consensus From INSPPIRE

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

Medical Management of Alagille Syndrome

Vascular anomalies in alagille syndrome: A significant cause of morbidity and mortality

Moyamoya Syndrome Associated with Alagille Syndrome: Outcome after Surgical Revascularization

Chromosome 10q23 Deletion Syndrome: An Overlap of Bannayan-Riley-Ruvalcaba Syndrome and Juvenile Polyposis Syndrome

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