Zobrazeno 1 - 10
of 280
pro vyhledávání: '"Peter F, Whitington"'
Autor:
Benjamin L Shneider, Jeff Moore, Nanda Kerkar, John C Magee, Wen Ye, Saul J Karpen, Binita M Kamath, Jean P Molleston, Jorge A Bezerra, Karen F Murray, Kathleen M Loomes, Peter F Whitington, Philip Rosenthal, Robert H Squires, Stephen L Guthery, Ronen Arnon, Kathleen B Schwarz, Yumirle P Turmelle, Averell H Sherker, Ronald J Sokol, Childhood Liver Disease Research Network
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176275 (2017)
INTRODUCTION:Optimizing outcome in biliary atresia (BA) requires timely diagnosis. Cholestasis is a presenting feature of BA, as well as other diagnoses (Non-BA). Identification of clinical features of neonatal cholestasis that would expedite decisio
Externí odkaz:
https://doaj.org/article/cb69c55e6c9c42809f1bb8f09a6520dc
Publikováno v:
Kompass Dermatologie. 9:231-236
Das juvenile Xanthogranulom (JXG) ist die häufigste Form der Non-Langerhans-Zell-Histiozytose. Es handelt sich um einen seltenen, angeborenen oder im späteren Alter auftretenden gutartigen Tumor. Die klassische Form des JXG ist durch rötlich-gelbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be47c2c451177d60dbdfe95e265bccd8
https://doi.org/10.1159/000519941
https://doi.org/10.1159/000519941
Autor:
Thomas N. Burn, Peter F. Whitington, Tomas Meijome, Kathleen M. Loomes, Hector Melin-Aldana, Estella M. Alonso, Portia A. Kreiger, Edward M. Behrens, Catherine A Chapin
Publikováno v:
Hepatology. 68:1087-1100
The cause of pediatric acute liver failure (PALF) is unknown in up to 40% of cases. Evidence suggests that aberrant immune system activation may play a role. We hypothesized that indeterminate PALF cases would exhibit a unique pattern of hepatic infl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ad085753f0ec0b5648b1657c5ccf73f
https://doi.org/10.1002/hep.29901
https://doi.org/10.1002/hep.29901
Autor:
Sarah A. Taylor, Harris Perlman, Joshua B. Wechsler, Peter F. Whitington, Kathryn E. Hulse, Padmini Malladi, Xiaomin Pan
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Biliary atresia (BA) is a neonatal cholestatic liver disease that is the leading cause of pediatric liver transplantation, however, the mechanism of disease remains unknown. There are two major forms of BA: isolated BA (iBA) comprises the majority of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee6a244999fa593941f698902831d6c8
https://doi.org/10.1038/s41598-019-41148-7
https://doi.org/10.1038/s41598-019-41148-7
Autor:
Sarah A. Taylor, Peter F. Whitington
Publikováno v:
Liver Transplantation. 22:677-685
Neonatal acute liver failure (NALF) is a rare disease about which there is little published data; however, NALF is an extremely important condition as it is distinct from acute liver failure seen in older children and adults. First, unlike acute live
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75963eb736881b2c81a42bf89345692b
https://doi.org/10.1002/lt.24433
https://doi.org/10.1002/lt.24433
Autor:
Stavra A. Xanthakos, Joel E. Lavine, Katherine P. Yates, Jeffrey B. Schwimmer, Jean P. Molleston, Philip Rosenthal, Karen F. Murray, Miriam B. Vos, Ajay K. Jain, Ann O. Scheimann, Tamir Miloh, Mark Fishbein, Cynthia A. Behling, Elizabeth M. Brunt, Arun J. Sanyal, James Tonascia, Stephanie Abrams, Donna Garner, Paula Hertel, Ryan Himes, Alicia Lawson, Nicole Triggs, Kristin Bramlage, April Carr, Kim Cecil, Meghan McNeill, Marialena Mouzaki, Andrew Trout, Stavra Xanthakos, Kimberlee Bernstein, Stephanie DeVore, Rohit Kohli, Kathleen Lake, Daniel Podberesky, Alex Towbin, Ali Mencin, Elena Reynoso, Adina Alazraki, Rebecca Cleeton, Maria Cordero, Albert Hernandez, Saul Karpen, Jessica Cruz Munos, Nicholas Raviele, Miriam Vos, Molly Bozic, Laura Carr, Oscar W. Cummings, Kathryn Harlow, Ann Klipsch, Emily Ragozzino, Girish Rao, Kimberly Kafka, Ann Scheimann, Mark H. Fishbein, Joy Ito, Saeed Mohammad, Peter F. Whitington, Sarah Barlow, Danielle Carpenter, Theresa Cattoor, Jose Derdoy, Janet Freebersyser, Ajay Jain, Debra King, Jinping Lai, Joan Siegner, Susan Stewart, Susan Torretta, Kristina Wriston, Jorge Angeles, Jennifer Arin, Cynthia Behling, Craig Bross, Carissa Carrier, Jennifer Collins, Diana De La Pena, Janis Durelle, Mary Catherine Huckaby, Michael S. Middleton, Kimberly Newton, Claude Sirlin, Patricia Ugalde-Nicalo, Jesse Courtier, Ryan Gill, Camille Langlois, Emily Rothbaum Perito, Patrika Tsai, Niviann Blondet, Kara Cooper, Karen Murray, Randolph Otto, Matthew Yeh, Melissa Young, Kathryn Fowler, David E. Kleiner, Edward C. Doo, Sherry Hall, Jay H. Hoofnagle, Patricia R. Robuck, Averell H. Sherker, Rebecca Torrance, Patricia Belt, Jeanne M. Clark, John Dodge, Michele Donithan, Milana Isaacson, Mariana Lazo, Jill Meinert, Laura Miriel, Emily P. Sharkey, Jacqueline Smith, Michael Smith, Alice Sternberg, Mark L. Van Natta, Annette Wagoner, Laura A. Wilson, Goro Yamada
Publikováno v:
Gastroenterology
BACKGROUND & AIMS: Nonalcoholic fatty liver disease (NAFLD) is the most common pediatric chronic liver disease. Little is known about outcomes in recognized youth. METHODS: We compared paired liver biopsies from 122 of 139 children with NAFLD (74% ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::959d37134cb442e61b520b5cf25732a4
https://doi.org/10.1053/j.gastro.2020.07.034
https://doi.org/10.1053/j.gastro.2020.07.034
Autor:
Richard J. Thompson, Giorgina Mieli-Vergani, Patricia McClean, Kaija-Leena Kolho, Jennifer L. Dodge, Irena Jankowska, Piotr Czubkowski, Ludmila Pawlikowska, Sami Wali, Florence Lacaille, Philip J. Rosenthal, Steven J. Lobritto, Vera Hupertz, Etienne Sokal, Karan M. Emerick, Sandra Strautnieks, Albertien M. van Eerde, Roderick H. J. Houwen, J A Byrne, Laura N. Bull, Peter F. Whitington, Catherine Wanty, Joanna Pawłowska, Samra Blanchard
Publikováno v:
Bull, L N, Pawlikowska, L, Strautnieks, S, Jankowska, I, Czubkowski, P, Dodge, J L, Emerick, K, Wanty, C, Wali, S, Blanchard, S, Lacaille, F, Byrne, J A, van Eerde, A M, Kolho, K-L, Houwen, R, Lobritto, S, Hupertz, V, McClean, P, Mieli-Vergani, G, Sokal, E, Rosenthal, P, Whitington, P F, Pawlowska, J & Thompson, R J 2018, ' Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies ', Hepatology Communications, vol. 2, no. 5, pp. 515-528 . https://doi.org/10.1002/hep4.1168
Hepatology communications, 2(5), 515. Wiley-Blackwell Publishing Ltd
Hepatology communications, vol 2, iss 5
Hepatology Communications
Hepatology communications, 2(5), 515. Wiley-Blackwell Publishing Ltd
Hepatology communications, vol 2, iss 5
Hepatology Communications
Progressive familial intrahepatic cholestasis (PFIC) with normal circulating gamma-glutamyl transpeptidase levels can result from mutations in the ATP8B1 gene (encoding familial intrahepatic cholestasis 1 [FIC1] deficiency) or the ABCB11 gene (bile s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec6a4e8d6de0b74ba0d5a189850110e
http://hdl.handle.net/10138/299438
http://hdl.handle.net/10138/299438
Autor:
Hector Melin-Aldana, Michael K. Fritsch, Padmini Malladi, Xiaomin Pan, Peter F. Whitington, C. Park
Publikováno v:
Journal of Neonatal-Perinatal Medicine. 8:23-31
Gestational alloimmune liver disease (GALD) is the result of neonatal complement-mediated severe liver injury mediated by maternal alloantibodies, which is detected by immunohistochemistry staining for the complement C5b-9 complex. GALD leads to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b19cef9376a50a6d6de1b8bdd7847979
https://doi.org/10.3233/npm-15814060
https://doi.org/10.3233/npm-15814060
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 60:659-663
Objectives:δ-Bilirubin (Bδ) forms when bilirubin conjugates covalently bind to albumin by way of nonenzymatic transesterification in patients with cholestasis. Infants with cholestasis with biliary atresia form Bδ. The aim of the present study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c13e5f9bff4f5098acf8aaf693b968ae
https://doi.org/10.1097/mpg.0000000000000690
https://doi.org/10.1097/mpg.0000000000000690
Autor:
Catherine A, Chapin, Thomas, Burn, Tomas, Meijome, Kathleen M, Loomes, Hector, Melin-Aldana, Portia A, Kreiger, Peter F, Whitington, Edward M, Behrens, Estella M, Alonso
Publikováno v:
Hepatology (Baltimore, Md.). 68(3)
The cause of pediatric acute liver failure (PALF) is unknown in up to 40% of cases. Evidence suggests that aberrant immune system activation may play a role. We hypothesized that indeterminate PALF cases would exhibit a unique pattern of hepatic infl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3c5941713269f7508425935bfc006fa
https://pubmed.ncbi.nlm.nih.gov/29603342
https://pubmed.ncbi.nlm.nih.gov/29603342