Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Scott A. Elisofon"'
Autor:
Nancy M. Rodig, Madison Weatherly, Abby L. Kaplan, Sonia Arora Ballal, Scott A. Elisofon, Kevin P. Daly, Stacy A. Kahn
Publikováno v:
Transplantation.
Autor:
Julia M. Boster, Riccardo Superina, George V. Mazariegos, Gregory M. Tiao, Jonathan P. Roach, Mark A. Lovell, Brian S. Greffe, George Yanni, Daniel H. Leung, Scott A. Elisofon, Suzanne V. McDiarmid, Nitika A. Gupta, Steven J. Lobritto, Caroline Lemoine, Janis M. Stoll, Bernadette E. Vitola, James F. Daniel, Blayne A. Sayed, Dev M. Desai, Abigail E. Martin, Arpit Amin, Ravinder Anand, Sarah G. Anderson, Shikha S. Sundaram
Publikováno v:
American Journal of Transplantation. 22:1396-1408
Management of unresectable pediatric hepatoblastoma (HB) and hepatocellular carcinoma (HCC) remains challenging. The Society of Pediatric Liver Transplantation (SPLIT) database was used to study survival predictors in pediatric liver transplantation
Autor:
James E. Squires, Shweta S. Namjoshi, Rachel Falik, Saeed Mohammad, Douglas Mogul, Ruba Azzam, Noelle H. Ebel, Mercedes Martinez, Steven J. Lobritto, Tamir Miloh, Nitika A. Gupta, Voytek Slowik, Linda S. Book, Vicky L. Ng, Bhavika Chepuri, Pamela L. Valentino, Daniel H. Leung, Mohit Kehar, Ming Hua Zheng, María C Sánchez, Ronen Arnon, Amit A. Shah, Christopher Chu, Quais Mujawar, Nadia K. Waheed, D. Kogan-Liberman, Jairo Eduardo Rivera Baquero, Scott A. Elisofon, Lisa Gallagher, Howard A. Kader, Bernadette Vitola, Nadia Ovchinsky, Leina Alrabadi, Amber Hildreth
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition
OBJECTIVE: Increased mortality risk because of severe acute respiratory syndrome coronavirus-2 (SARS-CoV2) infection in adults with native liver disease (LD) and liver transplant (LT) is associated with advanced age and comorbid conditions. We aim to
Autor:
Ann Wessel, Scott A. Elisofon, Mohammed Almuqbil, David J. Harris, Michael A. J. Ferguson, Didem Demirbas, William L. Nyhan, Tajinder P. Singh, Leah Hecht, Elizabeth D. Blume, Heung Bae Kim, Inderneel Sahai, Deborah Marsden, Gerard T. Berry
Publikováno v:
JIMD Reports, Vol 54, Iss 1, Pp 3-8 (2020)
JIMD Reports
JIMD Reports
Cardiomyopathy is a frequent complication of propionic acidemia (PA). It is often fatal, and its occurrence is largely independent of classic metabolic treatment modalities. Liver transplantation (LT) is a treatment option for severe PA as the liver
Autor:
Rachel Falik, M. H. Zheng, Nadia Ovchinsky, A. Sehgal, S. Lam, Ruba Azzam, Saeed Mohammad, D. Kogan-Liberman, B. Chepuri, J. E. R. Baqueros, L. Gallagher, Pamela L. Valentino, C. Chu, Douglas Mogul, Vicky L. Ng, James E. Squires, Ronen Arnon, S. S. Namjoshi, Noelle H. Ebel, Steven J. Lobritto, Mercedes Martinez, Leina Alrabadi, Tamir Miloh, Mohit Kehar, Daniel H. Leung, Howard A. Kader, María C Sánchez, Bernadette Vitola, Nitika A. Gupta, S. Lebel, Scott A. Elisofon, J. Botha, D. D'Agostino, Eyal Shteyer, Amit A. Shah, Quais Mujawar, Nadia K. Waheed, Linda S. Book, Voytek Slowik, N. Blondet, Amber Hildreth
Publikováno v:
Hepatology (Baltimore, Md.). 74
Autor:
Scott A. Elisofon, Andrew M. Lippa, Rima Fawaz, Karen E. Ocwieja, Julie Iglesias, Christine K. Lee, Tanvi Sharma
Publikováno v:
Transplant Infectious Disease. 22
A 20-year-old male presented 3.5 years after intestinal transplantation with rapidly progressive sensorineural hearing loss. Initial brain imaging was consistent with inflammation and/or demyelination. Lumbar puncture was initially non-diagnostic and
Autor:
Paul Mitchell, Maureen M. Jonas, Silvia Nastasio, Scott A. Elisofon, Khashayar Vakili, Denis D Nguyen, Heung Bae Kim, Christine K. Lee, Rima Fawaz
Publikováno v:
Pediatric transplantationREFERENCES. 24(6)
TE measures liver stiffness to assess fibrosis. Its use in post-transplant patients was reported in few small pediatric studies. We evaluated TE ability to predict liver graft fibrosis in a large cohort while comparing it to the performance of APRI a
Autor:
Scott A. Elisofon, Heung Bae Kim
Publikováno v:
Hepatology (Baltimore, Md.)References. 71(2)
IMPORTANCE: Some infants with biliary atresia are treated with primary liver transplant (pLT), but most are initially treated with biliary-enteric drainage (BED) with a subsequent salvage liver transplant. Given the improvements in liver transplant o
Autor:
Khashayar Vakili, Nancy Rodig, Heung Bae Kim, Gabriel Ramos-Gonzalez, Scott A. Elisofon, Eliza Lee
Publikováno v:
Pediatric Nephrology. 33:881-887
Primary hyperoxaluria type-1 (PH-1) is a rare genetic disorder in which normal hepatic metabolism of glyoxylate is disrupted resulting in diffuse oxalate deposition and end-stage renal disease (ESRD). While most centers agree that combined liver–ki
Autor:
Scott A, Elisofon, John C, Magee, Vicky L, Ng, Simon P, Horslen, Vicki, Fioravanti, Julie, Economides, Jinson, Erinjeri, Ravinder, Anand, George V, Mazariegos, R, Tomlin
Publikováno v:
Pediatric transplantationREFERENCES. 24(1)
BACKGROUND SPLIT was founded in 1995 in order to collect comprehensive prospective data on pediatric liver transplantation, including waiting list data, transplant, and early and late outcomes. Since 2011, data collection of the current registry has