Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nanda Kerkar"'
Autor:
Shannon M, Vandriel, Li-Ting, Li, Huiyu, She, Jian-She, Wang, Melissa A, Gilbert, Irena, Jankowska, Piotr, Czubkowski, Dorota, Gliwicz-Miedzińska, Emmanuel M, Gonzales, Emmanuel, Jacquemin, Jérôme, Bouligand, Nancy B, Spinner, Kathleen M, Loomes, David A, Piccoli, Lorenzo, D'Antiga, Emanuele, Nicastro, Étienne, Sokal, Tanguy, Demaret, Noelle H, Ebel, Jeffrey A, Feinstein, Rima, Fawaz, Silvia, Nastasio, Florence, Lacaille, Dominique, Debray, Henrik, Arnell, Björn, Fischler, Susan, Siew, Michael, Stormon, Saul J, Karpen, Rene, Romero, Kyung Mo, Kim, Woo Yim, Baek, Winita, Hardikar, Sahana, Shankar, Amin J, Roberts, Helen M, Evans, M Kyle, Jensen, Marianne, Kavan, Shikha S, Sundaram, Alexander, Chaidez, Palaniswamy, Karthikeyan, Maria Camila, Sanchez, Maria Lorena, Cavalieri, Henkjan J, Verkade, Way Seah, Lee, James E, Squires, Christina, Hajinicolaou, Chatmanee, Lertudomphonwanit, Ryan T, Fischer, Catherine, Larson-Nath, Yael, Mozer-Glassberg, Cigdem, Arikan, Henry C, Lin, Jesus Quintero, Bernabeu, Seema, Alam, Deirdre A, Kelly, Elisa, Carvalho, Cristina Targa, Ferreira, Giuseppe, Indolfi, Ruben E, Quiros-Tejeira, Pinar, Bulut, Pier Luigi, Calvo, Zerrin, Önal, Pamela L, Valentino, Dev M, Desai, John, Eshun, Maria, Rogalidou, Antal, Dezsőfi, Sabina, Wiecek, Gabriella, Nebbia, Raquel Borges, Pinto, Victorien M, Wolters, María Legarda, Tamara, Andréanne N, Zizzo, Jennifer, Garcia, Kathleen, Schwarz, Marisa, Beretta, Thomas Damgaard, Sandahl, Carolina, Jimenez-Rivera, Nanda, Kerkar, Jernej, Brecelj, Quais, Mujawar, Nathalie, Rock, Cristina Molera, Busoms, Wikrom, Karnsakul, Eberhard, Lurz, Ermelinda, Santos-Silva, Niviann, Blondet, Luis, Bujanda, Uzma, Shah, Richard J, Thompson, Bettina E, Hansen, Binita M, Kamath
Publikováno v:
Hepatology
Vandriel, S M, Li, L T, She, H, Wang, J S, Gilbert, M A, Jankowska, I, Czubkowski, P, Gliwicz-Miedzińska, D, Gonzales, E M, Jacquemin, E, Bouligand, J, Spinner, N B, Loomes, K M, Piccoli, D A, D'Antiga, L, Nicastro, E, Sokal, É, Demaret, T, Ebel, N H, Feinstein, J A, Fawaz, R, Nastasio, S, Lacaille, F, Debray, D, Arnell, H, Fischler, B, Siew, S, Stormon, M, Karpen, S J, Romero, R, Kim, K M, Baek, W Y, Hardikar, W, Shankar, S, Roberts, A J, Evans, H M, Jensen, M K, Kavan, M, Sundaram, S S, Chaidez, A, Karthikeyan, P, Sanchez, M C, Cavalieri, M L, Verkade, H J, Lee, W S, Squires, J E, Hajinicolaou, C, Lertudomphonwanit, C, Fischer, R T, Sandahl, T D & The Global ALagille Alliance (GALA) Study Group 2023, ' Natural history of liver disease in a large international cohort of children with Alagille syndrome : Results from the GALA study ', Hepatology, vol. 77, no. 2 . https://doi.org/10.1002/hep.32761
Hepatology, Vol. 77, no. 2, p. 512-529 (2023)
Vandriel, S M, Li, L T, She, H, Wang, J S, Gilbert, M A, Jankowska, I, Czubkowski, P, Gliwicz-Miedzińska, D, Gonzales, E M, Jacquemin, E, Bouligand, J, Spinner, N B, Loomes, K M, Piccoli, D A, D'Antiga, L, Nicastro, E, Sokal, É, Demaret, T, Ebel, N H, Feinstein, J A, Fawaz, R, Nastasio, S, Lacaille, F, Debray, D, Arnell, H, Fischler, B, Siew, S, Stormon, M, Karpen, S J, Romero, R, Kim, K M, Baek, W Y, Hardikar, W, Shankar, S, Roberts, A J, Evans, H M, Jensen, M K, Kavan, M, Sundaram, S S, Chaidez, A, Karthikeyan, P, Sanchez, M C, Cavalieri, M L, Verkade, H J, Lee, W S, Squires, J E, Hajinicolaou, C, Lertudomphonwanit, C, Fischer, R T, Sandahl, T D & The Global ALagille Alliance (GALA) Study Group 2023, ' Natural history of liver disease in a large international cohort of children with Alagille syndrome : Results from the GALA study ', Hepatology, vol. 77, no. 2 . https://doi.org/10.1002/hep.32761
Hepatology, Vol. 77, no. 2, p. 512-529 (2023)
Background and aims: Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real-world data are lacking. This study aimed to elucidate the natural history
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:
Douglas Mogul, Kyle Soltys, Greg Tiao, Frederick M. Karrer, Lee M. Bass, Matthew S. Clifton, Alexander Miethke, C. Azen, Mary L. Brandt, Peter Mattei, Philip J. Rosenthal, Nanda Kerkar, Saul J. Karpen, Cara L. Mack, Karen W. West, Kishore Iyer, Molly Bozic, Yumirle P. Turmelle, Dylan Stewart, Kasper S. Wang, Cat Goodhue, Jessica A. Zagory, Riccardo A. Superina, Patrick A. Dillon, Benjamin L. Shneider, Laura N. Bull, Binita M. Kamath, Ronen Arnon, Kathleen M. Loomes, Annie Fecteau, Paula M. Hertel
To evaluate the efficacy of nontransplant surgery for pediatric cholestasis, 58 clinically diagnosed children, including 20 with Alagille syndrome (ALGS), 16 with familial intrahepatic cholestasis-1 (FIC1), 18 with bile salt export pump (BSEP) diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e3c5bb539389909f391191c4a485b64
https://europepmc.org/articles/PMC5397365/
https://europepmc.org/articles/PMC5397365/
Autor:
Betsy C. Herold, Nanda Kerkar, Sukru Emre, Rebecca Pellett Madan, Benjamin L. Shneider, Gail F. Shust, Andrew L. Campbell, Birte Wistinghausen, Alissa R. Kahn, Roberto Posada
Publikováno v:
Transplantation. 87:1318-1324
Background This single center, retrospective study describes experience with a hybrid prevention strategy combining short-course antiviral prophylaxis and preemptive cytomegalovirus (CMV) polymerase chain reaction (PCR) monitoring. Methods One hundre
Publikováno v:
Clinical Gastroenterology and Hepatology. 7:239-245
Background & Aims Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease characterized by inflammation and progressive bile duct fibrosis. There are limited data on pediatric PSC. Methods We performed a retrospective chart review
Autor:
Scott S. Short, Stephanie Papillon, Nanda Kerkar, Colleen Azen, Kasper S. Wang, Philip Stanley, Catherine J. Hunter, Larry Wang
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 57(5)
The aim of this study was to determine patient factors that predict diagnostic failure or increased risk of bleeding complications following percutaneous liver biopsy in children.A retrospective review of all children undergoing percutaneous liver bi
Autor:
Fenella, Greig, Robert, Rapaport, Genna, Klein, Gidon, Akler, Rachel, Annunziato, Tamir, Miloh, Ronen, Arnon, Sander, Florman, Nanda, Kerkar
Publikováno v:
Pediatric transplantation. 17(1)
Studies of DALT in pediatric recipients describe incidence and risk factors, but diagnostic criteria varied. This study reports characteristics and course of pediatric DALT by established diabetes criteria. Retrospective chart review of pediatric LT
Autor:
Chana, Weiner, Lauren, Weintraub, Birte, Wistinghausen, Juli, Tomaino, Ronen, Arnon, Nanda, Kerkar, Tamir, Miloh
Publikováno v:
Pediatric transplantation. 16(5)
Treatment of primary EV and PTLD in pediatric LT recipients (pLT) involves IS reduction/cessation. Retrospective review of pLT at our institution from 2001-2009 was conducted to characterize risk factors for GR after EV/ PTLD. Of 184 pLT, EV occurred