B. Kamath

发表

Enteral energy and macronutrients in end-stage liver disease.

M. Mouzaki, V. Ng, B. Kamath, 2014, JPEN. Journal of parenteral and enteral nutrition.

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

I. Krantz, N. Spinner, B. Krock, 2019, Human mutation.

From Hepatocyte to Cholangiocyte: The Remarkable Potential of Transdifferentiation to Treat Cholestatic Diseases

B. Kamath, C. Mack, 2019, Hepatology.

Facial features in Alagille syndrome: specific or cholestasis facies?

I. Krantz, N. Spinner, B. Kamath, 2002, American journal of medical genetics.

Management of Pediatric Nonalcoholic Fatty Liver Disease by Academic Hepatologists in Canada: A Nationwide Survey

M. Mouzaki, B. Kamath, S. Ling, 2017, Journal of pediatric gastroenterology and nutrition.

The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration

F. Gottrand, T. Miloh, B. Kamath, 2017, Hepatology.

Assessment of School Readiness in Chronic Cholestatic Liver Disease: A Pilot Study Examining Children with and without Liver Transplantation

V. Ng, B. Kamath, A. Parmar, 2017, Canadian journal of gastroenterology & hepatology.

Longitudinal Outcomes in Young Patients with Alpha-1-Antitrypsin Deficiency with Native Liver Reveal that Neonatal Cholestasis is a Poor Predictor of Future Portal Hypertension.

P. Rosenthal, N. Kerkar, C. Spino, 2020, The Journal of pediatrics.

Baseline Analysis of a Young &agr;-1-Antitrypsin Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension

P. Rosenthal, R. Arnon, C. Spino, 2015, Journal of pediatric gastroenterology and nutrition.

Vascular Anomalies in Alagille Syndrome: A Significant Cause of Morbidity and Mortality

I. Krantz, N. Spinner, A. Chudley, 2004, Circulation.

Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference.

S. Hooper, M. Braun, L. Wilkins-Haug, 2014, The Journal of pediatrics.

Systematic Review: The Epidemiology, Natural History, and Burden of Alagille Syndrome

R. Houwen, N. Kerkar, B. Kamath, 2018, Journal of pediatric gastroenterology and nutrition.

Alagille syndrome: clinical perspectives

D. Chitayat, B. Kamath, M. Saleh, 2016, The application of clinical genetics.

Pathologic Lower Extremity Fractures in Children With Alagille Syndrome

N. Spinner, J. Shults, M. Leonard, 2010, Journal of pediatric gastroenterology and nutrition.

Heritable disorders of the bile ducts.

B. Kamath, D. Piccoli, 2003, Gastroenterology clinics of North America.

Hepatoblastoma in Explanted Livers of Patients With Biliary Atresia

V. Ng, B. Kamath, S. Ling, 2016, Journal of pediatric gastroenterology and nutrition.

Second-Line Agents in Pediatric Patients with Autoimmune Hepatitis: A Systematic Review and Meta-Analysis.

B. Kamath, P. Shah, P. Valentino, 2017, Journal of pediatric gastroenterology and nutrition.

Listeria meningitis after treatment with infliximab.

R. Baldassano, B. Kamath, P. Mamula, 2002, Journal of pediatric gastroenterology and nutrition.

Management of acute upper gastrointestinal bleeding

B. Kamath, P. Mamula, C. Liacouras, 2002 .

Superior Outcomes and Reduced Wait Times in Pediatric Recipients of Living Donor Liver Transplantation

V. Ng, B. Kamath, S. Ling, 2019, Transplantation direct.

Systematic review of progressive familial intrahepatic cholestasis.

R. Houwen, N. Kerkar, B. Kamath, 2019, Clinics and research in hepatology and gastroenterology.

Moyamoya syndrome associated with Alagille syndrome: outcome after surgical revascularization.

Edward R. Smith, N. Spinner, R. Ichord, 2015, The Journal of pediatrics.

Intracranial Vascular Abnormalities in Patients with Alagille Syndrome

I. Krantz, N. Spinner, B. Kamath, 2005, Journal of pediatric gastroenterology and nutrition.

Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome

Richard J. Thompson, David T. Okou, N. Spinner, 2019, Hepatology.

Alagille Syndrome

B. Kamath, Shannon M Vandriel, 2021, Pediatric Liver Transplantation.

Outcomes of liver transplantation for patients with alagille syndrome: The studies of pediatric liver transplantation experience

B. Kamath, H. Miller, E. Rand, 2012, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Medical management of Alagille syndrome.

B. Kamath, D. Piccoli, K. Loomes, 2010, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation

S. Scherer, J. Howe, S. Prescott, 2019, bioRxiv.

Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation

S. Scherer, J. Howe, S. Prescott, 2019, Stem cell reports.

Sarcopenia in Children With End-Stage Liver Disease

G. Chavhan, V. Ng, B. Kamath, 2017, Journal of pediatric gastroenterology and nutrition.

Paediatric reference values for total psoas muscle area

P. Jüni, G. Chavhan, V. Ng, 2020, Journal of cachexia, sarcopenia and muscle.

Pediatric living donor liver transplantation with large‐for‐size left lateral segment grafts

V. Ng, B. Kamath, S. Ling, 2019, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Acute Variceal Bleeding Causes Significant Morbidity

V. Ng, B. Kamath, S. Ling, 2018, Journal of pediatric gastroenterology and nutrition.

Consensus Recommendations for a Research Agenda in Exercise in Solid Organ Transplantation

L. Lands, M. Haykowsky, S. Marzolini, 2014 .

Unraveling the Relationship Between Itching, Scratch Scales, and Biomarkers in Children With Alagille Syndrome

P. Rosenthal, C. Spino, K. Setchell, 2020, Hepatology communications.

Frailty in liver transplantation: An expert opinion statement from the American Society of Transplantation Liver and Intestinal Community of Practice

A. Montano‐Loza, A. Duarte-Rojo, J. Lai, 2019, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Frailty in Children with Liver Disease: A Prospective Multicenter Study

T. Miloh, M. Englesbe, Henry C. Lin, 2018, The Journal of pediatrics.

Genotype correlates with the natural history of severe bile salt export pump deficiency.

Richard J. Thompson, B. Kamath, H. Arnell, 2020, Journal of hepatology.

Cholestatic liver diseases of genetic etiology: Advances and controversies

Samar H. Ibrahim, B. Kamath, S. Karpen, 2022, Hepatology.

Vascular Manifestations in Alagille Syndrome

R. Ichord, B. Kamath, Shannon M Vandriel, 2018 .

Monozygotic twins with a severe form of Alagille syndrome and phenotypic discordance.

I. Krantz, N. Spinner, B. Kamath, 2002, American journal of medical genetics.

Alagille Syndrome and JAGGED1/NOTCH Sequence

B. Kamath, D. Piccoli, K. Loomes, 2010 .

A girl with cystic fibrosis and failure to thrive.

B. Kamath, T. Scanlin, E. Ruchelli, 2003, The Journal of pediatrics.

Hepatic Issues and Complications Associated With Inflammatory Bowel Disease: A Clinical Report From the NASPGHAN Inflammatory Bowel Disease and Hepatology Committees.

R. Falcone, M. Jonas, Rohit Kohli, 2017, Journal of pediatric gastroenterology and nutrition.

Hepatic ultrastructural features distinguish paediatric Wilson disease from NAFLD and autoimmune hepatitis

B. Kamath, I. Siddiqui, E. Roberts, 2022, Liver international (Print).

Pediatric Wilson Disease Presenting as Acute Liver Failure: An Individual Patient Data Meta-Analysis.

V. Ng, B. Kamath, S. Ling, 2020, Journal of pediatric gastroenterology and nutrition.

Sarcopenia in Children With End‐Stage Liver Disease on the Transplant Waiting List

G. Chavhan, V. Ng, B. Kamath, 2021, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Gadobenate-dimeglumine-enhanced magnetic resonance imaging for hepatic lesions in children

P. Babyn, G. Chavhan, B. Kamath, 2014, Pediatric Radiology.

Potential of ileal bile acid transporter inhibition as a therapeutic target in Alagille syndrome and progressive familial intrahepatic cholestasis

R. Houwen, B. Kamath, H. Verkade, 2020, Liver international : official journal of the International Association for the Study of the Liver.

A national retrospective study of paediatric end‐stage liver disease as a predictor of change to second‐line therapy in children with autoimmune hepatitis

F. Alvarez, B. Kamath, S. Ling, 2017, Liver international : official journal of the International Association for the Study of the Liver.

Use of a Comprehensive 66-Gene Cholestasis Sequencing Panel in 2171 Cholestatic Infants, Children, and Young Adults

Richard J. Thompson, P. Rosenthal, R. Sokol, 2021, Journal of pediatric gastroenterology and nutrition.

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

Richard J. Thompson, N. Spinner, P. Rosenthal, 2020, Hepatology communications.

Pancreatic Insufficiency Is Not a Prevalent Problem in Alagille Syndrome

R. Sokol, B. Kamath, D. Piccoli, 2012, Journal of pediatric gastroenterology and nutrition.

Alagille syndrome in a Vietnamese cohort: Mutation analysis and assessment of facial features

I. Krantz, N. Spinner, B. Kamath, 2012, American journal of medical genetics. Part A.

SNP array mapping of 20p deletions: Genotypes, Phenotypes and Copy Number Variation

Joseph T. Glessner, I. Krantz, T. Shaikh, 2011 .

Alagille Syndrome and Liver Transplantation

N. Hadžić, B. Kamath, K. Schwarz, 2010, Journal of pediatric gastroenterology and nutrition.

Consequences of JAG1 mutations

I. Krantz, N. Spinner, B. Kamath, 2003, Journal of medical genetics.

Maralixibat Treatment Response in Alagille Syndrome Is Associated with Improved Health-Related Quality of Life.

B. Kamath, E. Jacquemin, E. Gonzales, 2022, The Journal of pediatrics.

Primary Sclerosing Cholangitis in Children With Inflammatory Bowel Diseases is Associated with Milder Clinical Activity but More Frequent Subclinical Inflammation and Growth Impairment.

M. Laeeq Khan, A. Griffiths, B. Kamath, 2020, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Hepatotoxicity Caused by Methotrexate Therapy in Children with Inflammatory Bowel Disease: A Systematic Review and Meta-analysis

A. Griffiths, J. Beyene, B. Feldman, 2014, Inflammatory bowel diseases.

Initial assessment of the infant with neonatal cholestasis—Is this biliary atresia?

P. Rosenthal, R. Arnon, N. Kerkar, 2017, PloS one.

Liver anomalies as a phenotype parameter of Bardet–Biedl syndrome

E. Héon, B. Kamath, V. Batmanabane, 2016, Clinical genetics.

Williams syndrome presenting with findings consistent with Alagille syndrome

H. Whyte, D. Chitayat, B. Kamath, 2014, Clinical case reports.

Inherited disorders of cholestasis in adulthood

B. Kamath, Lee M. Bass, 2013, Clinical liver disease.

A Longitudinal Study to Identify Laboratory Predictors of Liver Disease Outcome in Alagille Syndrome

N. Spinner, Zhongxue Chen, B. Kamath, 2010, Journal of pediatric gastroenterology and nutrition.

Magnetic Resonance Imaging Findings in Neonatal Hemochromatosis

G. Chavhan, B. Kamath, I. Siddiqui, 2017, Journal of pediatric gastroenterology and nutrition.

Intrahepatic Cholestasis Is a Clinically Significant Feature Associated with Natural History of X-Linked Myotubular Myopathy (XLMTM): A Case Series and Biopsy Report

B. Kamath, M. Lawlor, R. Graham, 2021, Journal of neuromuscular diseases.

Discovery of thyrocyte heterogeneity reveals an essential role of Notch signaling in thyroid function and mammalian homeostasis

Robert Piskol, B. Kamath, C. Siebel, 2022, bioRxiv.

Craniosynostosis in Alagille syndrome.

I. Krantz, N. Spinner, C. Stolle, 2002, American journal of medical genetics.

Cholangiocytes derived from induced pluripotent stem cells for disease modeling

B. Kamath, A. Ghanekar, 2016, Current opinion in gastroenterology.

Liver Disease in Pediatric Inflammatory Bowel Disease

B. Kamath, P. Valentino, 2013 .

Renal involvement and the role of Notch signalling in Alagille syndrome

N. Spinner, N. Rosenblum, B. Kamath, 2013, Nature Reviews Nephrology.

P. Rosenthal, J. Varni, N. Kerkar, 2013, The Journal of pediatrics.

Gut microbiome in primary sclerosing cholangitis: A review

A. Griffiths, B. Kamath, E. Wine, 2020, World journal of gastroenterology.

Liver transplantation in children: update 2010.

K. Olthoff, B. Kamath, 2010, Pediatric clinics of North America.

Odevixibat treatment in progressive familial intrahepatic cholestasis: a randomised, placebo-controlled, phase 3 trial.

Richard J. Thompson, L. D’Antiga, R. Houwen, 2022, The lancet. Gastroenterology & hepatology.

Directed differentiation of cholangiocytes from human pluripotent stem cells

Shinichiro Ogawa, Gordon Keller, Bin Li, 2015, Nature Biotechnology.

New Onset Autoimmune Hepatitis during Anti‐Tumor Necrosis Factor‐Alpha Treatment in Children

A. Griffiths, B. Kamath, S. Ling, 2017, The Journal of pediatrics.

Alagille Syndrome: Diagnostic Challenges and Advances in Management

B. Kamath, Mohammed D. Ayoub, 2020, Diagnostics.

Development of a Novel Tool to Assess the Impact of Itching in Pediatric Cholestasis

S. Medendorp, B. Kamath, A. Dorenbaum, 2017, The Patient - Patient-Centered Outcomes Research.

Early life predictive markers of liver disease outcome in an International, Multicentre Cohort of children with Alagille syndrome

N. Spinner, J. Beyene, P. Rosenthal, 2016, Liver international : official journal of the International Association for the Study of the Liver.

Renal anomalies in Alagille syndrome: A disease‐defining feature

I. Krantz, N. Spinner, B. Kamath, 2012, American journal of medical genetics. Part A.

NOTCH2 mutations in Alagille syndrome

I. Krantz, N. Spinner, P. Lapunzina, 2011, Journal of Medical Genetics.

SNP array mapping of chromosome 20p deletions: Genotypes, phenotypes, and copy number variation

Joseph T. Glessner, I. Krantz, N. Spinner, 2009, Human mutation.

Supernumerary digital flexion creases: an additional clinical manifestation of Alagille syndrome.

I. Krantz, B. Kamath, R. Oakey, 2002, American journal of medical genetics.

THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome

N. Spinner, M. Devoto, Michael M. Wang, 2016, Cellular and molecular gastroenterology and hepatology.

Serum biomarkers correlated with liver stiffness assessed in a multicenter study of pediatric cholestatic liver disease

Richard J. Thompson, O. Cummings, J. Hoofnagle, 2022, Hepatology.

Reply to correspondence from Kosztolányi and Méhes “Supernumerary digital flexion creases”

I. Krantz, B. Kamath, 2003 .

Liver transplantation for children with acute liver failure associated with secondary hemophagocytic lymphohistiocytosis

V. Ng, B. Kamath, S. Ling, 2016, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Nutritional Considerations In Pediatric Liver Transplantation

B. Kamath, E. Rand, A. Muir, 2009 .

Mutations in TJP2 cause progressive cholestatic liver disease

Colin A. Johnson, Richard J. Thompson, Joshua D. Smith, 2014, Nature Genetics.

Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3

I. Krantz, N. Spinner, H. Hakonarson, 2010, American journal of medical genetics. Part A.

Biliary complications in pediatric liver transplantation: Incidence and management over a decade

J. Seal, V. Ng, B. Kamath, 2015, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Burkholderia multivorans septicemia in a pediatric liver transplant patient

Y. Yau, V. Waters, J. Lipuma, 2018, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Magnetic resonance imaging of neonatal hemochromatosis

G. Chavhan, B. Kamath, I. Siddiqui, 2021, Pediatric Radiology.

Liver transplantation for Gaucher disease presenting as neonatal cholestasis: Case report and literature review

N. Sondheimer, B. Kamath, M. Inbar‐Feigenberg, 2020, Pediatric transplantation.

Menetrier's disease (protein-losing gastropathy) in a child with acute lymphoblastic leukemia

B. Kamath, C. Chung, A. Punnett, 2019, International journal of pediatrics & adolescent medicine.

Successful liver transplantation in an infant with stage 4S(M) neuroblastoma

S. Baruchel, V. Ng, B. Kamath, 2013, Pediatric blood & cancer.

A randomized clinical trial of age and genotype‐guided tacrolimus dosing after pediatric solid organ transplantation

M. Lafreniere-Roula, S. Mital, C. Manlhiot, 2018, Pediatric transplantation.

The role of diagnostic imaging and liver biopsy in the diagnosis of focal nodular hyperplasia in children

G. Chavhan, V. Ng, B. Kamath, 2014, Liver international : official journal of the International Association for the Study of the Liver.

Ursodeoxycholic Acid Therapy in Pediatric Primary Sclerosing Cholangitis: Predictors of Gamma Glutamyltransferase Normalization and Favorable Clinical Course.

T. Miloh, B. Kamath, K. Kolho, 2019, The Journal of pediatrics.

Liver Disease in Alagille Syndrome

B. Kamath, K. Loomes, Alyssa Kriegermeier, 2018 .

Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

Richard J. Thompson, M. H. Jørgensen, F. Suchy, 2022, JHEP Reports.

The Sclerosing Cholangitis Outcomes in Pediatrics (SCOPE) Index: A Prognostic Tool for Children

T. Miloh, N. Kerkar, S. Guthery, 2020, Hepatology.

Gamma Glutamyltransferase Reduction Is Associated With Favorable Outcomes in Pediatric Primary Sclerosing Cholangitis

F. Gottrand, T. Miloh, A. Tanaka, 2018, Hepatology communications.

Mutation Analysis and Disease Features at Presentation in a Multi-Center Cohort of Children With Monogenic Cholestasis

Richard J. Thompson, F. Suchy, R. Superina, 2021, Journal of pediatric gastroenterology and nutrition.

Bone Density in Children With Chronic Liver Disease Correlates With Growth and Cholestasis

P. Rosenthal, T. Hangartner, C. Spino, 2018, Hepatology.

Impact of Genotype, Serum Bile Acids, and Surgical Biliary Diversion on Native Liver Survival in FIC1 Deficiency

Richard J. Thompson, P. Rosenthal, F. Suchy, 2021, Hepatology.

Analysis of surgical interruption of the enterohepatic circulation as a treatment for pediatric cholestasis

P. Rosenthal, R. Arnon, K. Iyer, 2017, Hepatology.

Neurodevelopmental Outcomes in Children With Inherited Liver Disease and Native Liver

P. Rosenthal, R. Sokol, V. Ng, 2021, Journal of pediatric gastroenterology and nutrition.

Quality of Life and Its Determinants in a Multicenter Cohort of Children with Alagille Syndrome.

P. Rosenthal, R. Arnon, R. Sokol, 2015, The Journal of pediatrics.

PS-195-Predicting long-term outcome after surgical biliary diversion in Bsep-deficiency patients: Results from the NAPPED consortium

Richard J. Thompson, D. Wessel, B. Kamath, 2019, Journal of Hepatology.

Recurrence of Primary Sclerosing Cholangitis After Liver Transplant in Children: An International Observational Study

T. Miloh, N. Kerkar, M. Jonas, 2021, Hepatology.

Early Posthepatoportoenterostomy Predictors of Native Liver Survival in Biliary Atresia

E. O'Loughlin, E. Benchimol, V. Ng, 2017, Journal of pediatric gastroenterology and nutrition.

Impact of long‐term administration of maralixibat on children with cholestasis secondary to Alagille syndrome

R. Sokol, B. Kamath, Robert H. Squires, 2022, Hepatology communications.

Use of funded multicenter prospective longitudinal databases to inform clinical trials in rare diseases—Examination of cholestatic liver disease in Alagille syndrome

C. Spino, S. Guthery, B. Kamath, 2022, Hepatology communications.

Placebo‐Controlled Randomized Trial of an Intestinal Bile Salt Transport Inhibitor for Pruritus in Alagille Syndrome

P. Rosenthal, C. Spino, S. Guthery, 2018, Hepatology communications.

Recurrence of Primary Sclerosing Cholangitis after Liver Transplantation in Children: Data from the Pediatric PSC Consortium

F. Gottrand, T. Miloh, A. Tanaka, 2017 .

EP1230: EFFICACY AND SAFETY OF ODEVIXIBAT IN CHILDREN WITH PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS WITH PRIOR PARTIAL EXTERNAL BILIARY DIVERSION

Richard J. Thompson, B. Kamath, P. Horn, 2022, Gastroenterology.

Solitary Hepatic Nodule Adjacent to the Right Portal Vein: A Common Finding of Alagille Syndrome?

G. Chavhan, V. Ng, B. Kamath, 2016, Journal of pediatric gastroenterology and nutrition.

Dieulafoy's lesion and segmental dilatation of the small bowel: an uncommon cause of gastrointestinal bleeding.

R. Markowitz, D. von Allmen, M. Morowitz, 2004, Journal of pediatric surgery.

Symptoms Do Not Correlate With Findings From Colonoscopy in Children With Inflammatory Bowel Disease and Primary Sclerosing Cholangitis

A. Griffiths, B. Kamath, T. Walters, 2018, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Measurement of Hepatic Venous Pressure Gradient Is Feasible and Safe in Children

V. Ng, B. Kamath, S. Ling, 2013, Journal of pediatric gastroenterology and nutrition.

Abnormal Liver Biochemistry Is Common in Pediatric Inflammatory Bowel Disease: Prevalence and Associations

A. Griffiths, B. Feldman, B. Kamath, 2015, Inflammatory bowel diseases.

Primary sclerosing cholangitis and overlap features of autoimmune hepatitis: a coming of age or an age-ist problem?

P. Trivedi, G. Hirschfield, B. Kamath, 2023, Journal of hepatology.

The IBD and PSC Phenotypes of PSC-IBD

A. Griffiths, B. Kamath, A. Ricciuto, 2018, Current Gastroenterology Reports.

Magnetic Resonance Cholangiopancreatography Severity Predicts Disease Outcomes in Pediatric Primary Sclerosing Cholangitis: A Reliability and Validity Study

B. Kamath, P. Church, A. Amirabadi, 2019, Hepatology communications.

Findings in percutaneous trans-hepatic cholecysto-cholangiography in neonates and infants presenting with conjugated hyperbilirubinemia: emphasis on differential diagnosis and cholangiographic patterns

V. Ng, B. Kamath, Dimitri A. Parra, 2023, BMC Pediatrics.

Effect of Kasai Procedure on Hepatic Outcome in Alagille Syndrome

N. Spinner, B. Kamath, A. Flake, 2010, Journal of pediatric gastroenterology and nutrition.

A screening algorithm for the efficient exclusion of biliary atresia in infants with cholestatic jaundice.

V. Ng, B. Kamath, S. Ling, 2015, Journal of pediatric surgery.

Facial features in Alagille syndrome

I. Krantz, N. Spinner, B. Kamath, 2004 .

Modeling Outcomes in Children With Biliary Atresia With Native Liver After 2 Years of Age

P. Rosenthal, W. Ye, S. Harpavat, 2020, Hepatology communications.

Assessing the Validity of Adult-Derived Prognostic Models for Primary Sclerosing Cholangitis Outcomes in Children.

F. Gottrand, T. Miloh, S. Guthery, 2019, Journal of pediatric gastroenterology and nutrition.

Alagille Syndrome: Current Understanding of Pathogenesis, and Challenges in Diagnosis and Management.

B. Kamath, Mohammed D. Ayoub, 2022, Clinics in liver disease.

Management of Complications of Portal Hypertension in Adults and Children: Variceal Hemorrhage

B. Kamath, S. Ling, E. Heathcote, 2012 .

Basiliximab with delayed introduction of calcineurin inhibitors as a renal‐sparing protocol following liver transplantation in children with renal impairment

M. Mouzaki, V. Ng, B. Kamath, 2013, Pediatric transplantation.

Glatiramer acetate–induced acute hepatotoxicity in an adolescent with MS

B. Kamath, E. Yeh, N. Makhani, 2013, Neurology.

Interim results from an ongoing, open-label, single-arm trial of odevixibat in progressive familial intrahepatic cholestasis

Richard J. Thompson, L. D’Antiga, R. Houwen, 2023, JHEP reports : innovation in hepatology.

26 NOTCH2 MUTATIONS IN ALAGILLE SYNDROME

I. Krantz, N. Spinner, B. Kamath, 2011 .

V. Ng, B. Kamath, J. Woolfson, 2021, Liver Transplantation.

Nonfasted Liver Stiffness Correlates with Liver Disease Parameters and Portal Hypertension in Pediatric Cholestatic Liver Disease

P. Rosenthal, W. Ye, R. Merion, 2020, Hepatology communications.

Abdominal lymphatic system visibility, morphology, and abnormalities in children as seen on routine MCRP and its association with immune-mediated diseases

G. Chavhan, B. Kamath, Christopher Z. Lam, 2020, European Radiology.

Assessment of liver fibrosis using a 3-dimensional high-resolution late gadolinium enhancement sequence in children and adolescents with Fontan circulation

A. Dipchand, G. Chavhan, S. Yoo, 2023, European Radiology.

Identification of PKD1L1 Gene Variants in Children with the Biliary Atresia Splenic Malformation Syndrome

Richard J. Thompson, N. Spinner, R. Gibbs, 2019 .

Fat Soluble Vitamin Assessment and Supplementation in Cholestasis.

R. Sokol, B. Kamath, S. Karpen, 2022, Clinics in liver disease.

Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study

Richard J. Thompson, N. Spinner, J. Feinstein, 2022, Hepatology.

Management of adults with Alagille syndrome.

V. Keitel, B. Kamath, Mohammed D. Ayoub, 2023, Hepatology international.

Differing Effects of Rapamycin or Calcineurin Inhibitor on T‐Regulatory Cells in Pediatric Liver and Kidney Transplant Recipients

B. Kamath, W. Hancock, J. Goebel, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

A Comparison of Primary Sclerosing Cholangitis with and Without Associated Inflammatory Bowel Disease: Data from the Pediatric PSC Consortium

F. Gottrand, T. Miloh, A. Tanaka, 2017 .

Meeting Report: Consensus Recommendations for a Research Agenda in Exercise in Solid Organ Transplantation

L. Lands, M. Haykowsky, S. Marzolini, 2014, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Alagille syndrome.

I. Krantz, N. Spinner, B. Kamath, 1997, Journal of medical genetics.

Hepatoblastoma in Explanted Livers of Patients With Biliary Atresia

V. Ng, B. Kamath, S. Ling, 2016, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Hepatic Issues and Complications Associated With Inflammatory Bowel Disease: A Clinical Report From the NASPGHAN Inflammatory Bowel Disease and Hepatology Committees.

R. Falcone, M. Jonas, Rohit Kohli, 2017, Journal of pediatric gastroenterology and nutrition.

Directed differentiation of cholangiocytes from human pluripotent stem cells

G. Keller, M. Grompe, B. Kamath, 2015, Nature Biotechnology.

Chronic Cholestatic Liver Disease and its Management in Adults and Children

G. Hirschfield, B. Kamath, 2012 .

Raised serum transaminases: not always liver disease

G. Mieli-Vergani, A. Dhawan, B. Kamath, 2000, Archives of disease in childhood.

Loss of Mtm1 causes cholestatic liver disease in a model of X-linked myotubular myopathy

J. Dowling, B. Kamath, M. Lawlor, 2023, The Journal of clinical investigation.

Abnormal Liver Biochemistry Is Common in Pediatric Inflammatory Bowel Disease: Prevalence and Associations

A. Griffiths, B. Feldman, B. Kamath, 2015, Inflammatory bowel diseases.

A 14-month-old boy with hematochezia.

B. Kamath, D. Piccoli, P. Mamula, 2004, MedGenMed : Medscape general medicine.

Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3

I. Krantz, N. Spinner, H. Hakonarson, 2010, American journal of medical genetics. Part A.

Predictors of 6-year event-free survival in Alagille syndrome patients treated with maralixibat, an ileal bile acid transporter inhibitor

Richard J. Thompson, B. Kamath, E. Jacquemin, 2023, Hepatology.

The role of diagnostic imaging and liver biopsy in the diagnosis of focal nodular hyperplasia in children

G. Chavhan, V. Ng, B. Kamath, 2014, Liver international : official journal of the International Association for the Study of the Liver.

A pilot feasibility study of an ultrasound-based tool to assess muscle mass in children with liver disease

G. Chavhan, V. Ng, B. Kamath, 2023, Hepatology communications.

Human Mutation

I. Krantz, N. Spinner, B. Krock, 2019 .

The Application of Clinical Genetics Dovepress Alagille Syndrome: Clinical Perspectives

D. Chitayat, B. Kamath, M. Saleh, 2022 .

A Longitudinal Study to Identify Laboratory Predictors of Liver Disease Outcome in Alagille Syndrome

N. Spinner, Zhongxue Chen, B. Kamath, 2010, Journal of pediatric gastroenterology and nutrition.