Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kristin A. Meliambro"'
Autor:
Sally A. Hulton, Jaap W. Groothoff, Yaacov Frishberg, Michael J. Koren, J. Scott Overcash, Anne-Laure Sellier-Leclerc, Hadas Shasha-Lavsky, Jeffrey M. Saland, Wesley Hayes, Daniella Magen, Shabbir H. Moochhala, Martin Coenen, Eva Simkova, Sander F. Garrelfs, David J. Sas, Kristin A. Meliambro, Taylor Ngo, Marianne T. Sweetser, Bahru A. Habtemariam, John M. Gansner, Tracy L. McGregor, John C. Lieske
Publikováno v:
Kidney International Reports, Vol 7, Iss 3, Pp 494-506 (2022)
Introduction: Primary hyperoxaluria type 1 (PH1) is a rare genetic disease caused by hepatic overproduction of oxalate, leading to kidney stones, nephrocalcinosis, kidney failure, and systemic oxalosis. In the 6-month double-blind period (DBP) of ILL
Externí odkaz:
https://doaj.org/article/d1c32da830c840358e1a339f45ee8a45
Autor:
Benjamin O. Adegbite, Matthew H. Abramson, Victoria Gutgarts, Marcel F. Musteata, Kinsuk Chauhan, Alecia N. Muwonge, Kristin A. Meliambro, Steven P. Salvatore, Sebastian El Ghaity-Beckley, Marina Kremyanskaya, Bridget Marcellino, John O. Mascarenhas, Kirk N. Campbell, Lili Chan, Steven G. Coca, Ellin M. Berman, Edgar A. Jaimes, Evren U. Azeloglu
Publikováno v:
medRxiv
IntroductionDasatinib has been associated with nephrotoxicity. We sought to examine the incidence of proteinuria on dasatinib and determine potential risk factors that may increase dasatinib-associated glomerular injury.MethodsWe examine glomerular i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b094cfad1cf08e41e114ad9f348c8aa1
https://europepmc.org/articles/PMC10153335/
https://europepmc.org/articles/PMC10153335/
Autor:
Sally A. Hulton, Jaap W. Groothoff, Yaacov Frishberg, Michael J. Koren, J. Scott Overcash, Anne-Laure Sellier-Leclerc, Hadas Shasha-Lavsky, Jeffrey M. Saland, Wesley Hayes, Daniella Magen, Shabbir H. Moochhala, Martin Coenen, Eva Simkova, Sander F. Garrelfs, David J. Sas, Kristin A. Meliambro, Taylor Ngo, Marianne T. Sweetser, Bahru A. Habtemariam, John M. Gansner, Tracy L. McGregor, John C. Lieske
Publikováno v:
Kidney International Reports, 7(3), 494-506. Elsevier Inc.
Introduction: Primary hyperoxaluria type 1 (PH1) is a rare genetic disease caused by hepatic overproduction of oxalate, leading to kidney stones, nephrocalcinosis, kidney failure, and systemic oxalosis. In the 6-month double-blind period (DBP) of ILL