Zobrazeno 1 - 9
of 9
pro vyhledávání: '"For the Childhood Liver Disease Research Network (ChiLDReN)"'
Autor:
Benjamin L. Shneider, Binita M. Kamath, John C. Magee, Nathan P. Goodrich, Kathleen M. Loomes, Wen Ye, Cathie Spino, Estella M. Alonso, Jean P. Molleston, Jorge A. Bezerra, Kasper S. Wang, Saul J. Karpen, Simon P. Horslen, Stephen L. Guthery, Philip Rosenthal, Robert H. Squires, Ronald J. Sokol, for the Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Hepatology Communications, Vol 6, Iss 8, Pp 1910-1921 (2022)
Abstract The conduct of long‐term conventional randomized clinical trials in rare diseases is very difficult, making evidenced‐based drug development problematic. As a result, real‐world data/evidence are being used more frequently to assess ne
Externí odkaz:
https://doaj.org/article/4943757ba56340778b553a64b61dfc1f
Autor:
Benjamin L. Shneider, Nathan P. Goodrich, Wen Ye, Cindy Sawyers, Jean P. Molleston, Robert M. Merion, Daniel H. Leung, Saul J. Karpen, Binita M. Kamath, Laurel Cavallo, Kasper Wang, Jeffrey H. Teckman, James E. Squires, Shikha S. Sundaram, Philip Rosenthal, Rene Romero, Karen F. Murray, Kathleen M. Loomes, M. Kyle Jensen, Jorge A. Bezerra, Lee M. Bass, Ronald J. Sokol, John C. Magee, For the Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Hepatology Communications, Vol 4, Iss 11, Pp 1694-1707 (2020)
Elastographic measurement of liver stiffness is of growing importance in the assessment of liver disease. Pediatric experiences with this technique are primarily single center and limited in scope. The Childhood Liver Disease Research Network provide
Externí odkaz:
https://doaj.org/article/647571020799419cbe6477fa8ad3ebe4
Autor:
Binita M. Kamath, Cathie Spino, Richard McLain, John C. Magee, Emily M. Fredericks, Kenneth D. Setchell, Alexander Miethke, Jean P. Molleston, Cara L. Mack, Robert H. Squires, Estella M. Alonso, Karen F. Murray, Kathleen M. Loomes, M. Kyle Jensen, Saul J. Karpen, Philip Rosenthal, Danny Thomas, Ronald J. Sokol, Benjamin L. Shneider, for the Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Hepatology Communications, Vol 4, Iss 7, Pp 1012-1018 (2020)
Pruritus is a debilitating symptom for patients with Alagille syndrome (ALGS). In a previously reported trial of maralixibat, an investigational antipruritic agent, itching was assessed using a digital diary based on twice‐daily caregiver observati
Externí odkaz:
https://doaj.org/article/bb0995bcee5c43aa950f9efac0f78e7d
Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study
Autor:
Binita M. Kamath, Wen Ye, Nathan P. Goodrich, Kathleen M. Loomes, Rene Romero, James E. Heubi, Daniel H. Leung, Nancy B. Spinner, David A. Piccoli, Estella M. Alonso, Stephen L. Guthery, Saul J. Karpen, Cara L. Mack, Jean P. Molleston, Karen F. Murray, Philip Rosenthal, James E. Squires, Jeffrey Teckman, Kasper S. Wang, Richard Thompson, John C. Magee, Ronald J. Sokol, for the Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Hepatology Communications, Vol 4, Iss 3, Pp 387-398 (2020)
Alagille syndrome (ALGS) is an autosomal dominant multisystem disorder with cholestasis as a defining clinical feature. We sought to characterize hepatic outcomes in a molecularly defined cohort of children with ALGS‐related cholestasis. Two hundre
Externí odkaz:
https://doaj.org/article/447c90d603d64b7688e87239ee217567
Autor:
Leung, Daniel H., Sorensen, Lisa G., Ye, Wen, Hawthorne, Kieran, Ng, Vicky L., Loomes, Kathleen M., Fredericks, Emily M., Alonso, Estella M., Heubi, James E., Horslen, Simon P., Karpen, Saul J., Molleston, Jean P., Rosenthal, Philip, Sokol, Ronald J., Squires, Robert H., Wang, Kasper S., Kamath, Binita M., Magee, John C., Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition; Jan2022, Vol. 74 Issue 1, p96-103, 8p
Autor:
Berauer, John-Paul, Mezina, Anya I, Okou, David T, Sabo, Aniko, Muzny, Donna M, Gibbs, Richard A, Hegde, Madhuri R, Chopra, Pankaj, Cutler, David J, Perlmutter, David H, Bull, Laura N, Thompson, Richard J, Loomes, Kathleen M, Spinner, Nancy B, Rajagopalan, Ramakrishnan, Guthery, Stephen L, Moore, Barry, Yandell, Mark, Harpavat, Sanjiv, Magee, John C, Kamath, Binita M, Molleston, Jean P, Bezerra, Jorge A, Murray, Karen F, Alonso, Estella M, Rosenthal, Philip, Squires, Robert H, Wang, Kasper S, Finegold, Milton J, Russo, Pierre, Sherker, Averell H, Sokol, Ronald J, Karpen, Saul J, Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Hepatology (Baltimore, Md.), vol 70, iss 3
Biliary atresia (BA) is the most common cause of end-stage liver disease in children and the primary indication for pediatric liver transplantation, yet underlying etiologies remain unknown. Approximately 10% of infants affected by BA exhibit various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::b4f66a5f11894d65bb369e91d51469d0
https://escholarship.org/uc/item/6845b3c3
https://escholarship.org/uc/item/6845b3c3
Autor:
Russo, Pierre, Magee, John C, Anders, Robert A, Bove, Kevin E, Chung, Catherine, Cummings, Oscar W, Finegold, Milton J, Finn, Laura S, Kim, Grace E, Lovell, Mark A, Magid, Margret S, Melin-Aldana, Hector, Ranganathan, Sarangarajan, Shehata, Bahig M, Wang, Larry L, White, Frances V, Chen, Zhen, Spino, Catherine, Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
The American journal of surgical pathology, vol 40, iss 12
The liver biopsy guides diagnostic investigation and therapy in infants with undiagnosed cholestasis. Histologic features in the liver may also have prognostic value in the patient with biliary atresia (BA). We assessed the relative value of histolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::07e0420345fcab36120c2066096522c6
https://escholarship.org/uc/item/4vr0k0jg
https://escholarship.org/uc/item/4vr0k0jg
Autor:
Bass, Lee M., Shneider, Benjamin L., Henn, Lisa, Goodrich, Nathan P., Magee, John C., Childhood Liver Disease Research Network (ChiLDReN)
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition; Jun2019, Vol. 68 Issue 6, p763-767, 5p
Autor:
Antonia Felzen, Daan B.E. van Wessel, Emmanuel Gonzales, Richard J. Thompson, Irena Jankowska, Benjamin L. Shneider, Etienne Sokal, Tassos Grammatikopoulos, Agustina Kadaristiana, Emmanuel Jacquemin, Anne Spraul, Patryk Lipiński, Piotr Czubkowski, Nathalie Rock, Mohammad Shagrani, Dieter Broering, Emanuele Nicastro, Deirdre Kelly, Gabriella Nebbia, Henrik Arnell, Björn Fischler, Jan B.F. Hulscher, Daniele Serranti, Cigdem Arikan, Esra Polat, Dominique Debray, Florence Lacaille, Cristina Goncalves, Loreto Hierro, Gema Muñoz Bartolo, Yael Mozer-Glassberg, Amer Azaz, Jernej Brecelj, Antal Dezsőfi, Pier Luigi Calvo, Enke Grabhorn, Steffen Hartleif, Wendy J. van der Woerd, Binita M. Kamath, Jian-She Wang, Liting Li, Özlem Durmaz, Nanda Kerkar, Marianne Hørby Jørgensen, Ryan Fischer, Carolina Jimenez-Rivera, Seema Alam, Mara Cananzi, Noemie Laverdure, Cristina Targa Ferreira, Felipe Ordoñez Guerrero, Heng Wang, Valerie Sency, Kyung Mo Kim, Huey-Ling Chen, Elisa de Carvalho, Alexandre Fabre, Jesus Quintero Bernabeu, Aglaia Zellos, Estella M. Alonso, Ronald J. Sokol, Frederick J. Suchy, Kathleen M. Loomes, Patrick J. McKiernan, Philip Rosenthal, Yumirle Turmelle, Simon Horslen, Kathleen Schwarz, Jorge A. Bezerra, Kasper Wang, Bettina E. Hansen, Henkjan J. Verkade
Publikováno v:
JHEP Reports, 5(2):100626. Elsevier
JHEP reports : innovation in hepatology, 5(2):100626. Elsevier
Scientia
JHEP Reports, Vol. 5, no.2, p. 100626 (2023)
JHEP reports : innovation in hepatology, 5(2):100626. Elsevier
Scientia
JHEP Reports, Vol. 5, no.2, p. 100626 (2023)
Compound heterozygosity; Genotype; Phenotype Heterocigosidad compuesta; Genotipo; Fenotipo Heterozigositat composta; Genotip; Fenotip Background & Aims Bile salt export pump (BSEP) deficiency frequently necessitates liver transplantation in childhood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9a4bf0cbb88ad99b95105970a79be1
https://pure.eur.nl/en/publications/48dc60fd-d2f3-4015-b5b3-25d845d0ca1a
https://pure.eur.nl/en/publications/48dc60fd-d2f3-4015-b5b3-25d845d0ca1a