Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Nanda Kerkar"'
Autor:
Karen F. Murray, Ravi Jhaveri, Nanda Kerkar, Parvathi Mohan, Shikha S. Sundaram, Regino P. Gonzalez-Peralta, Chuan-Hao Lin, Daniel H. Leung, James E. Squires, Eve A. Roberts
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 71:407-417
In 1989, a collaboration between the Centers for Disease Control (CDC) and a California biotechnology company identified the hepatitis C virus (HCV, formerly known as non-A, non-B hepatitis virus) as the causative agent in the epidemic of silent post
Autor:
Bernadette Vitola, Christine K. Lee, Nanda Kerkar, Trevor J. Laborda, Kathleen M. Loomes, Kaija-Leena Kolho, Saeed Mohammed, Madeleine Aumar, Kathleen B. Schwarz, Alexandre Rodrigues Ferreira, Binita M. Kamath, Bart G. P. Koot, Cara L. Mack, Annemarie Broderick, Venna L. Venkat, Katryn N. Furuya, Mary Elizabeth M. Tessier, Girish S. Rao, Mercedes Martinez, Marek Woynarowski, Eleonora Druve Tavares Fagundes, Atsushi Tanaka, Tamir Miloh, Pamela L. Valentino, Laura G. Draijer, Douglas Mogul, Mark Deneau, Vratislav Smolka, Nitika A. Gupta, Amanda Ricciuto, Emily R. Perito, Melissa Zerofsky, Nadia Ovchinsky, Simon Horslen, Maureen M. Jonas, Kyung Mo Kim
Publikováno v:
Hepatology, 74(4), 2047-2057. John Wiley and Sons Ltd
Hepatology
Hepatology
Background and Aims Recurrent primary sclerosing cholangitis (rPSC) following liver transplant (LT) has a negative impact on graft and patient survival; little is known about risk factors for rPSC or disease course in children. Approach and Results W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb28e12c988d05385a8817b747a5af76
https://pure.amc.nl/en/publications/recurrence-of-primary-sclerosing-cholangitis-after-liver-transplant-in-children-an-international-observational-study(aab082d4-579e-4631-b00a-f340eb7d2081).html
https://pure.amc.nl/en/publications/recurrence-of-primary-sclerosing-cholangitis-after-liver-transplant-in-children-an-international-observational-study(aab082d4-579e-4631-b00a-f340eb7d2081).html
Autor:
Liting Li, Jian-She Wang, Ozlem Durmaz, Felipe Ordonez, Wikrom Karnsakul, Seema Alam, Cristina Targa Ferreira, Natural Course, Bettina E. Hansen, Kyung Mo Kim, Etienne Sokal, Ryan T. Fischer, Valerie Sency, Estella M. Alonso, Simon Horslen, Elisa de Carvalho, Piotr Czubkowski, Emanuele Nicastro, Nanda Kerkar, Dieter C. Broering, Björn Fischler, Dorothee Krebs-Schmitt, Kathleen M. Loomes, Dominique Debray, Marianne Hørby Jørgensen, Benjamin L. Shneider, Emmanuel Gonzales, Cigdem Arikan, Nathalie Rock, Antal Dezsőfi, Tassos Grammatikopoulos, Steffen Hartleif, Mara Cananzi, Talal Algoufi, Ronald J. Sokol, Jan B F Hulscher, Carolina Jimenez-Rivera, Emmanuel Jacquemin, Anne Spraul, Henkjan J. Verkade, Patryk Lipiński, Daan B E van Wessel, Nejat Mazhar, Maria Rogalidou, Deirdre Kelly, Alexandre Fabre, Daniele Serranti, Pier Luigi Calvo, Yael Mozer-Glassberg, Richard J. Thompson, Cristina Goncalves, Yumirle P. Turmelle, Jesus Quintero Bernabeu, Agustina Kadaristiana, Florence Lacaille, Loreto Hierro, Mohammad Shagrani, Patrick J. McKiernan, Girish S. Rao, Gema Muñoz Bartolo, Huey-Ling Chen, Wendy L. van der Woerd, Irena Jankowska, Amer Azaz, Philip J. Rosenthal, Frederick J. Suchy, Jernej Brecelj, Gabriella Nebbia, Noemie Laverdure, Henrik Arnell, Binita M. Kamath, Heng Wang
Publikováno v:
Hepatology
Hepatology, Wiley-Blackwell, 2021, 74 (2), pp.892-906. ⟨10.1002/hep.31787⟩
Hepatology, 74(2), 892-906. Wiley
Hepatology, Vol. 74, no. 2, p. 892-906 (2021)
Hepatology (Baltimore, Md.)
Hepatology, Wiley-Blackwell, 2021, 74 (2), pp.892-906. ⟨10.1002/hep.31787⟩
Hepatology, 74(2), 892-906. Wiley
Hepatology, Vol. 74, no. 2, p. 892-906 (2021)
Hepatology (Baltimore, Md.)
Mutations in ATP8B1 can lead to familial intrahepatic cholestasis type 1 (FIC1) deficiency, or progressive familial intrahepatic cholestasis type 1 (PFIC1). The rarity of FIC1 deficiency has largely prevented a detailed analysis of its natural histor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ecc4ae32d84b425ddef55c91928639e
https://hal-amu.archives-ouvertes.fr/hal-03663238
https://hal-amu.archives-ouvertes.fr/hal-03663238
Autor:
Pushpa Sathya, Jessica T. Hochberg, Wael El-Matary, Nadia Ovchinsky, Ruchi Singh, Trevor J. Laborda, Douglas Mogul, Matthew DiGuglielmo, Simon Horslen, Emily R. Perito, Maureen M. Jonas, Alexander Miethke, Bart G. P. Koot, Kathleen B. Schwarz, Girish S. Rao, Nitika A. Gupta, Pamela L. Valentino, Cara L. Mack, Mark Deneau, Katryn N. Furuya, Amanda Ricciuto, M. Kyle Jensen, Laura G. Draijer, Nanda Kerkar, Uzma Shah, Achiya Z. Amir, Stephen L. Guthery, Kathleen M. Loomes, Mercedes Martinez, Tamir Miloh, Andréanne Zizzo, Saeed Mohammad, Christine K. Lee, Bernadette Vitola
Publikováno v:
Hepatology
Background and aims Many children with primary sclerosing cholangitis (PSC) receive oral vancomycin therapy (OVT) or ursodeoxycholic acid (UDCA). There is a paucity of data on whether these medications improve outcomes. Approach and results We analyz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acf3b2ebfb947e045c1ea79b0999907f
https://europepmc.org/articles/PMC8557636/
https://europepmc.org/articles/PMC8557636/
Autor:
Matjaz Homan, Binita M. Kamath, Bart G. P. Koot, Mansi Amin, Parvathi Mohan, Amanda Ricciuto, Melissa Zerofsky, Madeleine Aumar, Kathleen B. Schwarz, Laura G. Draijer, Annemarie Broderick, Kaija-Leena Kolho, Stephen L. Guthery, Nanda Kerkar, Saeed Mohammad, Nisreen Soufi, Alexandra Papadopoulou, Eyal Shteyer, Raffaele Iorio, Nadia Ovchinsky, M. Kyle Jensen, Simon Horslen, Ruchi Singh, Maureen M. Jonas, Kyung Mo Kim, Alexander Miethke, Girish S. Rao, Federica Ferrari, Achiya Z. Amir, Cara L. Mack, Douglas Mogul, Matthew DiGuglielmo, Vratislav Smolka, Christine K. Lee, Pushpa Sathya, Katryn N. Furuya, Nitika A. Gupta, Mercedes Martinez, Atsushi Tanaka, Tamir Miloh, Kathleen M. Loomes, Bernadette Vitola, Uzma Shah, Pamela L. Valentino, Andréanne Zizzo, Mark Deneau, Jessica T. Hochberg, Wael El-Matary, Stacy Moroz, Marcus Auth, Emily R. Perito, Trevor J. Laborda, Marek Woynarowski, Eleonora Druve Tavares Fagundes, Alexandre Rodrigues Ferreira, Raghu Varier, Sirish Palle
Publikováno v:
Hepatology (Baltimore, Md.), 73(3), 1074-1087. John Wiley and Sons Ltd
Paediatrics Publications
Paediatrics Publications
Background and Aims: Disease progression in children with primary sclerosing cholangitis (PSC) is variable. Prognostic and risk-stratification tools exist for adult-onset PSC, but not for children. We aimed to create a tool that accounts for the bioc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::637d4623b2b71ae6a097d52eb99df8c2
https://pure.amc.nl/en/publications/the-sclerosing-cholangitis-outcomes-in-pediatrics-scope-index-a-prognostic-tool-for-children(92facea3-8fbb-41d6-adfd-46dfef3c90b7).html
https://pure.amc.nl/en/publications/the-sclerosing-cholangitis-outcomes-in-pediatrics-scope-index-a-prognostic-tool-for-children(92facea3-8fbb-41d6-adfd-46dfef3c90b7).html
Autor:
Cara L. Mack, Robert H Squires, Pinar Bulut, Saul J. Karpen, Ashutosh Gupta, Ravinder Anand, Matthew Ryan, Tamir Miloh, Benjamin L. Shneider, Chuan-Hao Lin, Ronen Arnon, Dennis Black, Pamela L. Valentino, Philip J. Rosenthal, Nanda Kerkar, Shikha S. Sundaram, Estella M. Alonso, Sarah H. Elsea
Publikováno v:
Hepatology Communications
Hepatology Communications, Vol 3, Iss 11, Pp 1482-1495 (2019)
Hepatology Communications, Vol 3, Iss 11, Pp 1482-1495 (2019)
Ursodeoxycholic acid (UDCA) is commonly used to treat several liver disorders in adults and children, including primary sclerosing cholangitis (PSC) for which it is not U.S. Food and Drug Administration approved. UDCA treatment has an uncertain impac
Autor:
Nanda Kerkar, Diego Vergani
Publikováno v:
Journal of Autoimmunity. 95:26-33
De novo autoimmune hepatitis (AIH) is an unusual cause of graft dysfunction after liver transplantation. This entity was originally described in 1996 in children transplanted for conditions other than AIH, who developed biochemical and histological f
Autor:
Cara L. Mack, Kathleen B. Schwarz, Jessica T. Hochberg, Wael El-Matary, Stacy Moroz, Trevor J. Laborda, Kathleen M. Loomes, Alexander Miethke, Girish S. Rao, Andréanne Zizzo, Nitika A. Gupta, Pamela L. Valentino, Nadia Ovchinsky, Nanda Kerkar, Pushpa Sathya, Mark Deneau, Ruchi Singh, Emily R. Perito, Achiya Z. Amir, Saeed Mohammed, Douglas Mogul, Matthew DiGuglielmo, Mercedes Martinez, Stephen L. Guthery, Bart G. P. Koot, Tamir Miloh, Simon Horslen, Amanda Ricciuto, Uzma Shah, Laura G. Draijer, Nisreen Soufi, Katryn N. Furuya
Publikováno v:
Clin Gastroenterol Hepatol
Inflammatory bowel disease (IBD), especially when associated with primary sclerosing cholangitis (PSC), is a risk factor for developing colorectal cancer (CRC).1-3 We aimed to determine the incidence of CRC in a large cohort of pediatric-onset PSC-ul
Autor:
Nanda Kerkar, Albert Chan
Publikováno v:
Clinics in liver disease. 22(4)
Autoimmune hepatitis (AIH) is characterized by elevated serum aminotransferases, immunoglobulin G, autoantibodies, and interface hepatitis, in the absence of a known diagnosis. Presentation is varied. Therapy is with immunosuppression. There is infla
Autor:
Jeffrey Teckman, Philip Rosenthal, Kieran Hawthorne, Cathie Spino, Lee M. Bass, Karen F. Murray, Nanda Kerkar, John C. Magee, Saul Karpen, James E. Heubi, Jean P. Molleston, Robert H. Squires, Binita M. Kamath, Stephen L. Guthery, Kathleen M. Loomes, Averell H. Sherker, Ronald J. Sokol, Estella Alonso, Lee Bass, Susan Kelly, Mary Riordan, Hector Melin-Aldana, Jorge Bezerra, Kevin Bove, James Heubi, Alexander Miethke, Greg Tiao, Julie Denlinger, Erin Chapman, Ronald Sokol, Amy Feldman, Cara Mack, Michael Narkewicz, Frederick Suchy, Shikha Sundaram, Johan Van Hove, Benigno Garcia, Mikaela Kauma, Kendra Kocher, Matthew Steinbeiss, Mark Lovell, Kathleen Loomes, David Piccoli, Elizabeth Rand, Pierre Russo, Nancy Spinner, Jessi Erlichman, Samantha Stalford, Dina Pakstis, Sakya King, Robert Squires, Rakesh Sindhi, Veena Venkat, Kathy Bukauskas, Patrick McKiernan, Lori Haberstroh, James Squires, Laura Bull, Joanna Curry, Camille Langlois, Grace Kim, Jeffery Teckman, Vikki Kociela, Rosemary Nagy, Shraddha Patel, Jacqueline Cerkoski, Molly Bozic, Girish Subbarao, Ann Klipsch, Cindy Sawyers, Oscar Cummings, Simon Horslen, Karen Murray, Evelyn Hsu, Kara Cooper, Melissa Young, Laura Finn, Binita Kamath, Vicky Ng, Claudia Quammie, Juan Putra, Deepika Sharma, Aishwarya Parmar, Stephen Guthery, Kyle Jensen, Ann Rutherford, Amy Lowichik, Linda Book, Rebecka Meyers, Tyler Hall, Kasper Wang, Sonia Michail, Danny Thomas, Catherine Goodhue, Rohit Kohli, Larry Wang, Nisreen Soufi, Daniel Thomas, Nitika Gupta, Rene Romero, Miriam B. Vos, Rita Tory, John-Paul Berauer, Carlos Abramowsky, Jeanette McFall, Benjamin Shneider, Sanjiv Harpavat, Paula Hertel, Daniel Leung, Mary Tessier, Deborah Schady, Laurel Cavallo, Diego Olvera, Christina Banks, Cynthia Tsai, Richard Thompson, Edward Doo, Jay Hoofnagle, Averell Sherker, Rebecca Torrance, Sherry Hall, John Magee, Robert Merion, Wen Ye
Publikováno v:
J Pediatr
Objectives To identify predictors of portal hypertension, liver transplantation, and death in North American youth with alpha-1-antitrypsin (AAT) deficiency, and compare with patients with AAT deficiency elsewhere. Study design The Childhood Liver Di