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

Author

Parra, Dimitri A., Peters, Shannon E., Kohli, Ruhail, Chamlati, Racha, Connolly, Bairbre L., Wolinska, Justyna M., Ng, Vicky L., Temple, Michael J., John, Philip R., Kamath, Binita M., Ling, Simon C., Fecteau, Annie, Amirabadi, Afsaneh, and Amaral, Joao G.

Published
2023
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3. International Liver Transplantation Society Global Census: First Look at Pediatric Liver Transplantation Activity Around the World

Author

Rodriguez-Davalos, Manuel I., Lopez-Verdugo, Fidel, Kasahara, Mureo, Muiesan, Paolo, Reddy, Mettu S., Flores-Huidobro Martinez, Angel, Xia, Qiang, Hong, Johnny C., Niemann, Claus U., Seda-Neto, Joao, Miloh, Tamir A., Yi, Nam-Joon, Mazariegos, George V., Ng, Vicky L., Esquivel, Carlos O., Lerut, Jan, Rela, Mohamed, Botha, Jean, Mehta, Naimish N., Bakar Hafeez Bhatti, Abu, Zamora-Valdes, Daniel, Anand, Superina, Riccardo, de Kleine, Ruben, Matamoros, Maria A., Bedregal-Mendoza, Tayana, Steve Bynon, J., Rodriguez-Sancho, Luis C., Langnas, Alan, Dhawan, Anil, Ogura, Yasuhiro, Vianna, Rodrigo, Ilyassova, Bibigul, Tantemsapya, Niramol, Bellemare, Sarah, Ovchinsky, Nadia, Bhalerao, Suryabhan, Balci, Deniz, Dip, Marcelo, Imventarza, Oscar, Mangus, Richard S., Fawcett, Jonathan, Antonini, Teresa M., Shrimal, Anurag, Zhu, Zhi-Jun, Rivera, Jairo, Dayangac, Murat, McCall, John, Utz Melere, Melina, Stormon, Michael, Mizuta, Koichi, Gao, Wei, Hening Rahayatri, Tri, Costaguta, Alejandro, Gautier, Sergei, Kazemi, Kourosh, Martinez-Castillo, Jorge, Apinyachon, Worapot, Rastogi, Mukul, Restrepo, Juan C., Takahito, Yagi, Ravichandra, Srinivasa, Vanin, Anabel, Vieira, Sandra, Luque, Carlos, Gondolesi, Gabriel, Hashimoto, Koji, Yazigi, Nada, Lebel, Sylvie, Mavis, Alisha, Arnon, Ronen, Chavez-Vargas, Ricardo, Elisofon, Scott, Desai, Dev M., Okajima, Hideaki, Chinnakotla, Srinath, Hsu, Evelyn, Reyes, Jorge, Orgoi, Sergelen, Raut, Vikram, Hee Oh, Seak, Valentino, Pamela, Emre, Sukru, Spada, Marco, Leung, Dan, Charco, Ramon, Ericzon, Bo-Goran, Fischer, Ryan, Del Rio-Martin, Juan V., Cillo, Umberto, Soliman, Hossam, Varela-Fascinetto, Gustavo, de Villa, Vanessa, Haberal, Mehmet, Covarrubias, Joshue, Colledan, Michele, de Ville de Goyet, Jean, Desai, Chirag, Sundaram, Shikha, Fronek, Jiri, Nadig, Satish N., Mali, Vidyadhar P., Tandoi, Francesco, Kohli, Rohit, Mohan, Neelam, Goyal, Neerav, Santhosh, Drisya, Debray, Dominique, Durmaz, Ozlem, De Bruyne, Ruth, Kaliciński, Piotr, Hierro, Loreto, Venick, Robert, Perito, Emily, Mozer-Glassberg, Yael, Chen, Chao-Long, Rand, Elizabeth, Nikeghbalian, Saman, Kelly, Deirdre, Boillot, Olivier, and Book, Linda S.

Published
2023
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4. Evidence of Chronic Allograft Injury in Liver Biopsies From Long-term Pediatric Recipients of Liver Transplants

Author

Feng, Sandy, Bucuvalas, John C, Demetris, Anthony J, Burrell, Bryna E, Spain, Katherine M, Kanaparthi, Sai, Magee, John C, Ikle, David, Lesniak, Andrew, Lozano, Juan J, Alonso, Estella M, Bray, Robert A, Bridges, Nancy E, Doo, Edward, Gebel, Howard M, Gupta, Nitika A, Himes, Ryan W, Jackson, Annette M, Lobritto, Steven J, Mazariegos, George V, Ng, Vicky L, Rand, Elizabeth B, Sherker, Averell H, Sundaram, Shikha, Turmelle, Yumirle P, and Sanchez-Fueyo, Alberto

Subjects
Biomedical and Clinical Sciences, Clinical Sciences, Chronic Liver Disease and Cirrhosis, Transplantation, Liver Disease, Clinical Research, Rare Diseases, Digestive Diseases, Genetics, Organ Transplantation, Oral and gastrointestinal, Adolescent, Allografts, Biopsy, Child, Chronic Disease, Cross-Sectional Studies, Female, Graft Rejection, Humans, Liver, Liver Function Tests, Liver Transplantation, Male, Time Factors, Young Adult, ALT, DSA, Immune Response, Prognostic Factor, Neurosciences, Paediatrics and Reproductive Medicine, Gastroenterology & Hepatology, Clinical sciences, Nutrition and dietetics
Abstract

Background & aimsA substantial proportion of pediatric liver transplant recipients develop subclinical chronic allograft injury. We studied whether there are distinct patterns of injury based on histopathologic features and identified associated immunologic profiles.MethodsWe conducted a cross-sectional study of 157 stable, long-term pediatric recipients of transplanted livers (70 boys; > 6 years old at time of transplantation; mean, 8.9 ± 3.46 years after liver transplantation) who underwent liver biopsy analysis from August 13, 2012, through May 1, 2014. Participants had received livers from a living or deceased donor and had consistently normal results from liver tests. Liver biopsy specimens were scored by a central pathologist; an unsupervised hierarchical cluster analysis of histologic features was used to sort biopsy samples into 3 clusters. We conducted transcriptional and cytometric analyses of liver tissue samples and performed a systems biology analysis that incorporated clinical, serologic, histologic, and transcriptional data.ResultsThe mean level of alanine aminotransferase in participants was 27.6 ± 14.57 U/L, and the mean level of γ-glutamyl transferase was 17.4 ± 7.93 U/L. Cluster 1 was characterized by interface activity (n = 34), cluster 2 was characterized by periportal or perivenular fibrosis without interface activity (n = 45), and cluster 3 had neither feature (n = 78). We identified a module of genes whose expression correlated with levels of alanine aminotransferase, class II donor-specific antibody, portal inflammation, interface activity, perivenular inflammation, portal and perivenular fibrosis, and cluster assignment. The module was enriched in genes that regulate T-cell-mediated rejection (TCMR) of liver and other transplanted organs. Functional pathway analysis showed overrepresentation of TCMR gene sets for cluster 1 but not clusters 2 or 3.ConclusionIn an analysis of biopsies from an apparently homogeneous group of stable, long-term pediatric liver transplant recipients with consistently normal liver test results, we found evidence of chronic graft injury (inflammation and/or fibrosis). Biopsy samples with interface activity had a gene expression pattern associated with TCMR.

Published
2018

9. Impact of early immunosuppression on pediatric liver transplant outcomes within 1 year

Author

Raghu, Vikram K., primary, Zhang, Xingyu, additional, Squires, James E., additional, Eisenberg, Elizabeth, additional, Feldman, Amy G., additional, Halma, Jennifer, additional, Peters, Anna L., additional, Gonzalez‐Peralta, Regino P., additional, Ng, Vicky L., additional, Horslen, Simon P., additional, Lobritto, Steven J., additional, Bucuvalas, John, additional, Mazariegos, George V., additional, and Perito, Emily R., additional

Published
2024
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14. Total Serum Bilirubin Predicts Fat‐Soluble Vitamin Deficiency Better Than Serum Bile Acids in Infants With Biliary Atresia

Author

Venkat, Veena L, Shneider, Benjamin L, Magee, John C, Turmelle, Yumirle, Arnon, Ronen, Bezerra, Jorge A, Hertel, Paula M, Karpen, Saul J, Kerkar, Nanda, Loomes, Kathleen M, Molleston, Jean, Murray, Karen F, Ng, Vicky L, Raghunathan, Trivellore, Rosenthal, Philip, Schwartz, Kathleen, Sherker, Averell H, Sokol, Ronald J, Teckman, Jeffrey, Wang, Kasper, Whitington, Peter F, Heubi, James E, and Network, Childhood Liver Disease Research and Education

Subjects
Biomedical and Clinical Sciences, Nutrition and Dietetics, Digestive Diseases, Clinical Research, Nutrition, Chronic Liver Disease and Cirrhosis, Liver Disease, Perinatal Period - Conditions Originating in Perinatal Period, Rare Diseases, Pediatric, Avitaminosis, Bile Acids and Salts, Biliary Atresia, Bilirubin, Dietary Supplements, Double-Blind Method, Female, Humans, Infant, Infant, Newborn, Male, National Institute of Diabetes and Digestive and Kidney Diseases (U.S.), Placebos, Prospective Studies, United States, Vitamin A, Vitamin D, Vitamin E, Vitamin K, Vitamins, biliary atresia, bilirubin, cholestasis, fat-soluble vitamin, serum bile acid, Childhood Liver Disease Research and Education Network, Medical and Health Sciences, Gastroenterology & Hepatology, Clinical sciences, Nutrition and dietetics, Paediatrics
Abstract

ObjectiveFat-soluble vitamin (FSV) deficiency is a well-recognized consequence of cholestatic liver disease and reduced intestinal intraluminal bile acid. We hypothesized that serum bile acid (SBA) would predict biochemical FSV deficiency better than serum total bilirubin (TB) level in infants with biliary atresia.MethodsInfants enrolled in the Trial of Corticosteroid Therapy in Infants with Biliary Atresia after hepatoportoenterostomy were the subjects of this investigation. Infants received standardized FSV supplementation and monitoring of TB, SBA, and vitamin levels at 1, 3, and 6 months. A logistic regression model was used with the binary indicator variable insufficient/sufficient as the outcome variable. Linear and nonparametric correlations were made between specific vitamin measurement levels and either TB or SBA.ResultsThe degree of correlation for any particular vitamin at a specific time point was higher with TB than with SBA (higher for TB in 31 circumstances vs 3 circumstances for SBA). Receiver operating characteristic curve shows that TB performed better than SBA (area under the curve 0.998 vs 0.821). Including both TB and SBA did not perform better than TB alone (area under the curve 0.998).ConclusionsWe found that TB was a better predictor of FSV deficiency than SBA in infants with biliary atresia. The role of SBA as a surrogate marker of FSV deficiency in other cholestatic liver diseases, such as progressive familial intrahepatic cholestasis, α-1-antitrypsin deficiency, and Alagille syndrome in which the pathophysiology is dominated by intrahepatic cholestasis, warrants further study.

Published
2014

15. Paediatric steatotic liver disease has unique characteristics: A multisociety statement endorsing the new nomenclature.

Author

Baumann, Ulrich, Koot, Bart G. P., Fitzpatrick, Emer, Mann, Jake, Vajro, Pietro, Krag, Aleksander, Newsome, Philip N., Shawcross, Debbie, Francque, Sven, Böttler, Tobias, Gold, Benjamin D., Lightdale, Jenifer R., Mouzaki, Marialena, Rodriguez‐Baez, Norberto, Kohli, Rohit, Ng, Vicky L., D'Agostino, Daniel, Porta, Gilda, Spolidoro, José, and Klünder‐Klünder, Miguel

Published
2024
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16. A Learning Collaborative Approach Increases Specificity of Diagnosis of Acute Liver Failure in Pediatric Patients

Author

Squires, Robert H., Bukauskas, Kathryn, Schulte, Madeline, Narkewicz, Michael R., Hite, Michelle, Loomes, Kathleen M., Rand, Elizabeth B., Piccoli, David, Kawchak, Deborah, Seidman, Christa, Romero, Rene, Karpen, Saul, de la Cruz-Tracy, Liezl, Ng, Vicky, Hunt, Kelsey, Subbarao, Girish C., Klipsch, Ann, Munson, Sarah, Alonso, Estella M., Sorenson, Lisa, Kelly, Susan, Neighbors, Katie, Rosenthal, Philip, Fleck, Shannon, Leonis, Mike A., Bucuvalas, John, Horning, Tracie, Rodriguez Baez, Norberto, Montanye, Shirley, Cowie, Margaret, Horslen, Simon P., Murray, Karen, Young, Melissa, Nielson, Heather, Klein, Jani, Rudnick, David A., Shepherd, Ross W., Harris, Kathy, Karpen, Saul J., De La Torre, Alejandro, Dell Olio, Dominic, Kelly, Deirdre, Lloyd, Carla, Lobritto, Steven J., Bakhsh, Sumerah, Jonas, Maureen, Elifoson, Scott A., Raza, Roshan, Schwarz, Kathleen B., Karnsakul, Wikrom W., Alford, Mary Kay, Dhawan, Anil, Fitzpatrick, Emer, Shneider, Benjamin L., Kerkar, Nanda N., Haydel, Brandy, Narayanappa, Sreevidya, Lopez, M. James, Shieck, Victoria, Doo, Edward, Sherker, Averell H., Belle, Steven H., Horslen, Simon, Hardison, Regina M., Rodriguez-Baez, Norberto, Ng, Vicky L., and Li, Ruosha

Published
2018
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17. Health Related Quality of Life and Neurocognitive Outcomes in the First Year after Pediatric Acute Liver Failure

Author

Bukauskas, Kathryn, Schulte, Madeline, Narkewicz, Michael R., Hite, Michelle, Rand, Elizabeth B., Piccoli, David, Kawchak, Deborah, Seidman, Christa, Romero, Rene, Karpen, Saul, de la Cruz-Tracy, Liezl, Hunt, Kelsey, Subbarao, Girish C., Klipsch, Ann, Munson, Sarah, Kelly, Susan, Rosenthal, Philip J., Fleck, Shannon, Leonis, Mike A., Bucuvalas, John, Horning, Tracie, Baez, Norberto Rodriguez, Montanye, Shirley, Cowie, Margaret, Horslen, Simon P., Murray, Karen, Young, Melissa, Nielson, Heather, Klein, Jani, Rudnick, David A., Shepherd, Ross W., Harris, Kathy, Karpen, Saul J., De La Torre, Alejandro, Dell Olio, Dominic, Kelly, Deirdre, Lloyd, Carla, Lobritto, Steven J., Bakhsh, Sumerah, Jonas, Maureen, Elifoson, Scott A., Raza, Roshan, Schwarz, Kathleen B., Karnsakul, Wikrom W., Alford, Mary Kay, Dhawan, Anil, Fitzpatrick, Emer, Kerkar, Nanda N., Haydel, Brandy, Narayanappa, Sreevidya, Lopez, M. James, Shieck, Victoria, Sorensen, Lisa G., Neighbors, Katie, Hardison, Regina M., Loomes, Kathleen M., Varni, James W., Ng, Vicky L., Squires, Robert H., and Alonso, Estella M.

Published
2018
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18. Neurodevelopmental Outcome of Young Children with Biliary Atresia and Native Liver: Results from the ChiLDReN Study

Author

Hertel, Paula M., Harpavat, Sanjiv, Brandt, Mary L., Leung, Daniel H., Karnsakul, Wikrom, Torrance, Rebecca, Hall, Sherry, Doo, Edward, Hoofnagle, Jay H., Whitington, Peter, Bass, Lee, Miethke, Alexander G., Heubi, James E., Setchell, Kenneth, Bove, Kevin E., Tiao, Greg, Mack, Cara L., Narkewicz, Michael R., Feldman, Amy G., Sundaram, Shikha S., Suchy, Frederick J., Karrer, Frederick M., Lovell, Mark, Van Hove, Johan L., Rand, Elizabeth B., Squires, James E., Venkat, Veena L., Sindhi, Rakesh, Ranganathan, Sarangarajan, Bull, Laura, Teckman, Jeffrey, Bozic, Molly, Subbarao, Girish, Horslen, Simon, Hsu, Evelyn, Finn, Laura, Healey, Patrick, Kohli, Rohit, Thomas, Danny, Soufi, Nisreen, Michail, Sonia, Clifton, Matt, Gupta, Nitika, Romero, Rene, Vos, Miriam, Caltharp, Shelley, Kamath, Binita M., Ling, Simon C., Gold, Anna, Fecteau, Annie, Guthery, Stephen L., Jensen, Kyle, Meyers, Rebecka, Lowichik, Amy, Book, Linda, Merion, Robert M., Spino, Cathie, Jones, Karen, Ng, Vicky L., Sorensen, Lisa G., Alonso, Estella M., Fredericks, Emily M., Ye, Wen, Moore, Jeff, Karpen, Saul J., Shneider, Benjamin L., Molleston, Jean P., Bezerra, Jorge A., Murray, Karen F., Loomes, Kathleen M., Rosenthal, Philip, Squires, Robert H., Wang, Kasper, Arnon, Ronen, Schwarz, Kathleen B., Turmelle, Yumirle P., Haber, Barbara H., Sherker, Averell H., Magee, John C., and Sokol, Ronald J.

Published
2018
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20. Frailty in Children with Liver Disease: A Prospective Multicenter Study

Author

Lurz, Eberhard, Quammie, Claudia, Englesbe, Michael, Alonso, Estella M., Lin, Henry C., Hsu, Evelyn K., Furuya, Katryn N., Gupta, Nitika A., Venkat, Veena L., Daniel, James F., Leonis, Mike A., Miloh, Tamir, Telega, Grzegorz W., Yap, Jason, Menendez, Jerome, Book, Linda S., Himes, Ryan W., Sundaram, Shikha S., Parekh, Rulan, Sonnenday, Chris, Bucuvalas, John, Ng, Vicky L., and Kamath, Binita M.

Published
2018
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21. Extrahepatic Anomalies in Infants With Biliary Atresia: Results of a Large Prospective North American Multicenter Study

Author

Schwarz, Kathleen B, Haber, Barbara H, Rosenthal, Philip, Mack, Cara L, Moore, Jeffrey, Bove, Kevin, Bezerra, Jorge A, Karpen, Saul J, Kerkar, Nanda, Shneider, Benjamin L, Turmelle, Yumirle P, Whitington, Peter F, Molleston, Jean P, Murray, Karen F, Ng, Vicky L, Romero, René, Wang, Kasper S, Sokol, Ronald J, Magee, John C, and Network, Childhood Liver Disease Research and Education

Subjects
Perinatal Period - Conditions Originating in Perinatal Period, Congenital Structural Anomalies, Chronic Liver Disease and Cirrhosis, Liver Disease, Prevention, Pediatric, Clinical Research, Cardiovascular, Rare Diseases, Digestive Diseases, 2.1 Biological and endogenous factors, Aetiology, Abnormalities, Multiple, Adult, Biliary Atresia, Female, Humans, Male, Prospective Studies, United States, Childhood Liver Disease Research and Education Network, Medical Biochemistry and Metabolomics, Clinical Sciences, Immunology, Gastroenterology & Hepatology
Abstract

UnlabelledThe etiology of biliary atresia (BA) is unknown. Given that patterns of anomalies might provide etiopathogenetic clues, we used data from the North American Childhood Liver Disease Research and Education Network to analyze patterns of anomalies in infants with BA. In all, 289 infants who were enrolled in the prospective database prior to surgery at any of 15 participating centers were evaluated. Group 1 was nonsyndromic, isolated BA (without major malformations) (n = 242, 84%), Group 2 was BA and at least one malformation considered major as defined by the National Birth Defects Prevention Study but without laterality defects (n = 17, 6%). Group 3 was syndromic, with laterality defects (n = 30, 10%). In the population as a whole, anomalies (either major or minor) were most prevalent in the cardiovascular (16%) and gastrointestinal (14%) systems. Group 3 patients accounted for the majority of subjects with cardiac, gastrointestinal, and splenic anomalies. Group 2 subjects also frequently displayed cardiovascular (71%) and gastrointestinal (24%) anomalies; interestingly, this group had genitourinary anomalies more frequently (47%) compared to Group 3 subjects (10%).ConclusionThis study identified a group of BA (Group 2) that differed from the classical syndromic and nonsyndromic groups and that was defined by multiple malformations without laterality defects. Careful phenotyping of the patterns of anomalies may be critical to the interpretation of both genetic and environmental risk factors associated with BA, allowing new insight into pathogenesis and/or outcome.

Published
2013

23. Immunosuppression-Free Life after Pediatric Liver Transplant: A Case-Control Study from the Society of Pediatric Liver Transplant (SPLIT) Registry

Author

Kortbeek, Simone, primary, Anderson, Sarah G., additional, Alonso, Estella M., additional, Rand, Elizabeth B., additional, Bucuvalas, John, additional, Mazariegos, George V., additional, Campbell, Kathleen M., additional, Lobritto, Steven J., additional, Feldman, Amy G., additional, Mysore, Krupa R., additional, Anand, Ravinder, additional, Selzner, Nazia, additional, and Ng, Vicky L., additional

Published
2023
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30. Advancing the Field of Pediatric Liver Transplantation: Urgent Action Items Identified During the 2022 Society of Pediatric Liver Transplantation Meeting

Author

Feldman, Amy G., primary, Adams, Megan, additional, Griesemer, Adam D., additional, Horslen, Simon, additional, Kelly, Beau, additional, Mavis, Alisha M., additional, Mazariegos, George V., additional, Ng, Vicky L., additional, Perito, Emily R., additional, Rodriguez-Davalos, Manuel I., additional, Squires, James E., additional, Tiao, Greg, additional, Yanni, George S., additional, and Hsu, Evelyn K., additional

Published
2023
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32. Total Serum Bilirubin within 3 Months of Hepatoportoenterostomy Predicts Short-Term Outcomes in Biliary Atresia

Author

Alonso, Estella, Kaurs, Elizabeth, Kelly, Sue, Bove, Kevin, Heubi, James, Miethke, Alexander, Tiao, Greg, Denlinger, Julie, Ferris, Andrea, Feldman, Amy, Mack, Cara, Suchy, Frederick, Sundaram, Shikha, Van Hove, Johan, Hite, Michelle, Kantor, Susanna, Miller, Todd, Smith, Julia, VanWinkle, Becky, Loomes, Kathleen, Lin, Henry, Piccoli, David, Russo, Pierre, Spinner, Nancy, Brown, Lindsay, Elgert, Emily, Erlichman, Jessi, Alissa, Feras, Lindblad, Douglas, Mazariegos, George, Ortiz-Aguayo, Roberto, Perlmutter, David, Sindhi, Rakesh, Venkat, Veena, Vockley, Jerry, Bukauskas, Kathy, Kufen, Adam, Schulte, Madeline, Bull, Laura, Fleck, Shannon, Langlois, Camille, Teckman, Jeffery, Kociela, Vikki, Postma, Stacy, Harris, Kathleen, Bozic, Molly, Subbarao, Girish, Byam, Beth, Klipsch, Ann, Sawyers, Cindy, Horslen, Simon, Hsu, Evelyn, Cooper, Kara, Young, Melissa, Kamath, Binita, DeAngelis, Maria, O'Connor, Constance, VanRoestel, Krista, Parmar, Arpita, Quammie, Claudia, Hung, Kelsey, Guthery, Stephen, Jensen, Kyle, Rutherford, Ann, Kerker, Nanda, Michail, Sonia, Thomas, Danny, Goodhue, Catherine, Gupta, Nikita, Vos, Mariam, de la Cruz-Tracey, Liezl, Hankerson-Dyson, Dana, Tory, Rita, Turner-Green, Taieshia, Wellons, Allison, Brandt, Mary, Finegold, Milton, Harpavat, Sanjiv, Hertel, Paula, Leung, Daniel, Liwanag, Loriel, Thompson, Richard, Brown, Sherry, Doo, Edward, Hoofnagle, Jay, Hall, Sherry, Torrance, Rebecca, Brown, Jameisha, Kafka, Kimberly, Merion, Robert, Spino, Cathie, Shneider, Benjamin L., Magee, John C., Karpen, Saul J., Rand, Elizabeth B., Narkewicz, Michael R., Bass, Lee M., Schwarz, Kathleen, Whitington, Peter F., Bezerra, Jorge A., Kerkar, Nanda, Haber, Barbara, Rosenthal, Philip, Turmelle, Yumirle P., Molleston, Jean P., Murray, Karen F., Ng, Vicky L., Wang, Kasper S., Romero, Rene, Squires, Robert H., Arnon, Ronen, Sherker, Averell H., Moore, Jeffrey, Ye, Wen, and Sokol, Ronald J.

Published
2016
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33. Hepatite aigue grave d'etiologie inconnue chez les enfants

Author

Science, Michelle, Campigotto, Aaron, and Ng, Vicky L.

Subjects
Hepatitis -- Health aspects -- Care and treatment -- Cases, Diseases -- Causes and theories of causation, Company legal issue, Health
Abstract

1 Des agences de sante publique a l'echelle de la planete se sont dites preoccupees des nombreux cas d'hepatite aigue grave d'etiologie inconnue chez les enfants En date du 8 [...]

Published
2022
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35. Similarities and Differences in Allocation Policies for Pediatric Liver Transplantation Across the World

Author

Fischler, Björn, Baumann, Ulrich, D’Agostino, Daniel, D’Antiga, Lorenzo, Dezsofi, Antal, Debray, Dominique, Durmaz, Ozlem, Evans, Helen, Frauca, Esteban, Hadzic, Nedim, Jahnel, Jörg, Loveland, Jerome, McLin, Valérie, Ng, Vicky L., Nobili, Valerio, Pawłowska, Joanna, Sharif, Khalid, Smets, Francoise, Verkade, Henkjan J., Hsu, Evelyn, Horslen, Simon, and Bucuvalas, John

Published
2019
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43. Health Care Transition for Adolescents and Young Adults With Pediatric-Onset Liver Disease and Transplantation: A Position Paper by the North American Society of Pediatric Gastroenterology, Hepatology, and Nutrition

Author

Vittorio, Jennifer, primary, Kosmach-Park, Beverly, additional, King, Lindsay Y., additional, Fischer, Ryan, additional, Fredericks, Emily M., additional, Ng, Vicky L., additional, Narang, Amrita, additional, Rasmussen, Sara, additional, and Bucuvalas, John, additional

Published
2022
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48. Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in children.

Author

Squires, James E., Miethke, Alexander G., Valencia, C. Alexander, Hawthorne, Kieran, Henn, Lisa, Van Hove, Johan L. K., Squires, Robert H., Bove, Kevin, Horslen, Simon, Kohli, Rohit, Molleston, Jean P., Romero, Rene, Alonso, Estella M., Bezerra, Jorge A., Guthery, Stephen L., Hsu, Evelyn, Karpen, Saul J., Loomes, Kathleen M., Ng, Vicky L., and Rosenthal, Philip

Published
2023
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