Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Shashi K. Nagaraj"'
Autor:
Kyle W. Freischlag, Vivian Chen, Shashi K. Nagaraj, Annabelle N. Chua, Dongfeng Chen, Delbert R. Wigfall, John W. Foreman, Rasheed Gbadegesin, Deepak Vikraman, Eileen T. Chambers
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Background: Currently, there is no standardized approach for determining psychosocial readiness in pediatric transplantation. We examined the utility of the Psychosocial Assessment of Candidates for Transplantation (PACT) to identify pediatric kidney
Externí odkaz:
https://doaj.org/article/cc24796b041746e198695f1a7621d694
Autor:
Annette M. Jackson, Del Wigfall, John W. Foreman, Rasheed Gbadegesin, Allan D. Kirk, Eileen Tsai Chambers, Shashi K. Nagaraj, Annabelle N. Chua, Rebecca E Sadun, Kathryn H. Blew
Publikováno v:
American Journal of Transplantation. 20:884-888
Adolescent transplant recipients are at risk for nonadherence, development of de novo donor-specific antibody (dnDSA), and allograft loss. Belatacept, a selective T cell costimulatory blocker, is associated with reduced dnDSA, improved renal function
Autor:
Sunil Babu, Guilia Antognoli, Elena Gutierréz, Yoshitaka Miyakawa, Moglie Le Quintrec, Jan Menne, David J. Kavanagh, Tatiana Kirsanova, Edwin K.S. Wong, Maria Vinogradova, Philip Campbell, Guillaume Favre, Michael Fischereder, Spero R. Cataland, Iino Fumie, Hermann Haller, Vladimir A. Dobronravov, Paramit Chowdhury, Guillaume Jeantet, Marie Scully, Sonia Boyer-Suavet, Thomas D. Barbour, Yosu Luque, Leonardo Caroti, Stephan Ortiz, Shashi K. Nagaraj, Cyril Garrouste, Masayoshi Okumi, Anja Gaeckler, Maria Cappuccilli, Chiu-Ching Huang, Anja Muhlfeld, Gema Ariceta, Gaetano La Manna, Eric Rondeau, Nils Heyne, Giorgia Comai, Natalia Ramos Terrada, Eric Goffin, Paola Rodriguez, Gregory Greenwood, Eugene Swenson, Barbara Seitz-Polski, Nilufer Broeders, Gowthami M. Arepally, Manuel Praga Terente, Marc Vallee, Johan Morelle, Siân V. Griffin, Nicole Lietar, Doyeun Oh, Theo Kasimatis, I-Ru Chen, Ulf Schönermarck, Susan Huang, Jin Seok Kim, Fiona G. Brown, François Provôt, Lino Cirami, Sung-Soo Yoon, Yahsou Delmas
Publikováno v:
Kidney international, Vol. 97, no.6, p. 1287-1296 (2020)
Kidney International
Kidney International, Nature Publishing Group, 2020, 97, pp.1287-1296. ⟨10.1016/j.kint.2020.01.035⟩
Kidney international, Vol. 97, no. 6, p. 1287-1296 (2020)
Kidney International
Kidney International, Nature Publishing Group, 2020, 97, pp.1287-1296. ⟨10.1016/j.kint.2020.01.035⟩
Kidney international, Vol. 97, no. 6, p. 1287-1296 (2020)
Ravulizumab is a long-acting C5 inhibitor engineered from eculizumab with increased elimination half-life, allowing an extended dosing interval from two to eight weeks. Here we evaluate the efficacy and safety of ravulizumab in adults with atypical h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::645216d81d77d6e0af0d5786a23bf3d8
https://hdl.handle.net/2078.1/240266
https://hdl.handle.net/2078.1/240266
Autor:
Holger Prokisch, Evan H. Baugh, Valentina Del Dotto, Michele Carbonelli, Rocco Liguori, Mirjana Gusic, Wolfgang Sperl, Tommaso Pippucci, Nicholas Stong, Pamela Magini, Enrico Bertini, William C. Copeland, Alessandra Maresca, Francesca Diomedi-Camassei, Shashi K. Nagaraj, Ioana Cutcutache, Bertil Macao, Alessandro Iannaccone, Francesco Emma, Piero Barboni, Marco Seri, Vandana Shashi, Zsolt Szilagyi, Farid Ullah, Camille Peron, Valerio Carelli, Chiara La Morgia, Ivano Di Meo, Martin Armstrong, Jennifer A. Sullivan, Saskia B. Wortmann, Nicholas Katsanis, Leonardo Caporali, Kamal Khan, Maria Falkenberg, Valeria Tiranti, Mays A. El-Dairi, Erica E. Davis, Maria Lucia Valentino, Margaret A. Gustafson, Claudia Zanna, Rosalba Carrozzo, Sylvia Boesch, Flavia Palombo, Francesca Tagliavini, Robert Kopajtich, Matthew Page
Publikováno v:
J. Clin. Invest. 130, 108-125 (2020)
Inherited optic neuropathies include complex phenotypes, mostly driven by mitochondrial dysfunction. We report an optic atrophy spectrum disorder, including retinal macular dystrophy and kidney insufficiency leading to transplantation, associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f59384a409cfa55c80cfd8e64162ba11
https://europepmc.org/articles/PMC6934201/
https://europepmc.org/articles/PMC6934201/
Autor:
David T. Selewski, Tarak Srivastava, Shashi K. Nagaraj, Eileen D. Brewer, Jennifer D. Varner, Rachel M Engen, Christoph Licht, Cynthia Silva, John Barcia, Christoph P. Hornik, Annabelle N. Chua, Delbert R. Wigfall, Rasheed Gbadegesin, Adam Bensimhon, Natasha Jawa, Patricia L. Weng, Caroline Straatmann, Michelle N. Rheault, Jonathan H. Pelletier, Scott E. Wenderfer, Karan R. Kumar, Eileen Tsai Chambers, T. Keefe Davis, Keisha L. Gibson, Mahmoud Kallash, John W. Foreman, Larry A. Greenbaum
Publikováno v:
Pediatric Nephrology. 33:1773-1780
BACKGROUND AND OBJECTIVES: Steroid resistant nephrotic syndrome (SRNS) due to focal segmental glomerulosclerosis (FSGS) and minimal change disease (MCD) is a leading cause of end stage kidney disease in children. Recurrence of primary disease followi
Autor:
Himani Vaidya, Sherry S. Ross, John S. Wiener, Shan Elahi, Adebowale Adeyemo, Shashi K. Nagaraj, Delbert R. Wigfall, Rasheed Gbadegesin, Patrick D. Brophy, Indra R. Gupta, Guanghong Wu, Jonathan C. Routh, John W. Foreman, Gentzon Hall, C. Egla Rabinovich, Alison Homstad, Peter J. Conlon, Jennifer Stout
Publikováno v:
Pediatric Nephrology. 31:247-253
Primary vesicoureteral reflux (PVUR) is the most common malformation of the kidney and urinary tract, and reflux nephropathy is a major cause of chronic kidney disease in children. Recently, we reported mutations in the tenascin XB gene (TNXB) as a c
Autor:
David N. Howell, Michelle P. Winn, John W. Foreman, Paul J. Phelan, Gentzon Hall, Andrew F. Malone, Delbert R. Wigfall, Shashi K. Nagaraj, Rasheed Gbadegesin
Publikováno v:
Clinical Kidney Journal
Background Mutations in podocin (NPHS2) are the most common cause of childhood onset autosomal recessive steroid-resistant nephrotic syndrome (SRNS). The disease is characterized by early-onset proteinuria, resistance to immunosuppressive therapy and
Autor:
Loren D.M. Pena, Yong-Hui Jiang, Kelly Schoch, Rebecca C. Spillmann, Nicole Walley, Nicholas Stong, Sarah Rapisardo Horn, Jennifer A. Sullivan, Allyn McConkie-Rosell, Sujay Kansagra, Edward C. Smith, Mays El-Dairi, Jane Bellet, Martha Ann Keels, Joan Jasien, Peter G. Kranz, Richard Noel, Shashi K. Nagaraj, Robert K. Lark, Daniel S.G. Wechsler, Daniela del Gaudio, Marco L. Leung, Laura G. Hendon, Collette C. Parker, Kelly L. Jones, David B. Goldstein, Vandana Shashi, Mercedes E. Alejandro, Carlos A. Bacino, Ashok Balasubramanyam, Bret L. Bostwick, Lindsay C. Burrage, Shan Chen, Gary D. Clark, William J. Craigen, Shweta U. Dhar, Lisa T. Emrick, Brett H. Graham, Neil A. Hanchard, Mahim Jain, Seema R. Lalani, Brendan H. Lee, Richard A. Lewis, Mashid S. Azamian, Paolo M. Moretti, Sarah K. Nicholas, Jordan S. Orange, Jennifer E. Posey, Lorraine Potocki, Jill A. Rosenfeld, Susan L. Samson, Daryl A. Scott, Alyssa A. Tran, Tiphanie P. Vogel, Jing Zhang, Hugo J. Bellen, Michael F. Wangler, Shinya Yamamoto, Christine M. Eng, Donna M. Muzny, Patricia A. Ward, Yaping Yang, Yong-hui Jiang, Nicole M. Walley, Alan H. Beggs, Lauren C. Briere, Cynthia M. Cooper, Laurel A. Donnell-Fink, Elizabeth L. Krieg, Joel B. Krier, Sharyn A. Lincoln, Joseph Loscalzo, Richard L. Maas, Calum A. MacRae, J. Carl Pallais, Lance H. Rodan, Edwin K. Silverman, Joan M. Stoler, David A. Sweetser, Chris A. Walsh, Cecilia Esteves, Ingrid A. Holm, Isaac S. Kohane, Paul Mazur, Alexa T. McCray, Matthew Might, Rachel B. Ramoni, Kimberly Splinter, David P. Bick, Camille L. Birch, Braden E. Boone, Donna M. Brown, Daniel C. Dorset, Lori H. Handley, Howard J. Jacob, Angela L. Jones, Jozef Lazar, Shawn E. Levy, J. Scott Newberry, Molly C. Schroeder, Kimberly A. Strong, Elizabeth A. Worthey, Jyoti G. Dayal, David J. Eckstein, Sarah E. Gould, Ellen M. Howerton, Donna M. Krasnewich, Laura A. Mamounas, Teri A. Manolio, John J. Mulvihill, Tiina K. Urv, Anastasia L. Wise, Ariane G. Soldatos, Matthew Brush, Jean-Philippe F. Gourdine, Melissa Haendel, David M. Koeller, Jennifer E. Kyle, Thomas O. Metz, Katrina M. Waters, Bobbie-Jo M. Webb-Robertson, Euan A. Ashley, Jonathan A. Bernstein, Annika M. Dries, Paul G. Fisher, Jennefer N. Kohler, Daryl M. Waggott, Matthew T. Wheeler, Patricia A. Zornio, Patrick Allard, Hayk Barseghyan, Esteban C. Dell'Angelica, Ani Dillon, Katrina M. Dipple, Naghmeh Dorrani, Emilie D. Douine, Ascia Eskin, Brent L. Fogel, Matthew R. Herzog, Hane Lee, Allen Lipson, Sandra K. Loo, Julian A. Martínez-Agosto, Stan F. Nelson, Christina G.S. Palmer, Jeanette C. Papp, Neil H. Parker, Janet S. Sinsheimer, Eric Vilain, Allison Zheng, Christopher J. Adams, Elizabeth A. Burke, Katherine R. Chao, Mariska Davids, David D. Draper, Tyra Estwick, Trevor S. Frisby, Kate Frost, Valerie Gartner, Rena A. Godfrey, Mitchell Goheen, Gretchen A. Golas, Mary G. Gordon, Catherine A. Groden, Mary E. Hackbarth, Isabel Hardee, Jean M. Johnston, Alanna E. Koehler, Lea Latham, Yvonne L. Latour, C. Christopher Lau, Denise J. Levy, Adam P. Liebendorfer, Ellen F. Macnamara, Valerie V. Maduro, Thomas C. Markello, Alexandra J. McCarty, Jennifer L. Murphy, Michele E. Nehrebecky, Donna Novacic, Barbara N. Pusey, Sarah Sadozai, Katherine E. Schaffer, Prashant Sharma, Sara P. Thomas, Nathanial J. Tolman, Camilo Toro, Zaheer M. Valivullah, Colleen E. Wahl, Mike Warburton, Alec A. Weech, Guoyun Yu, Andrea L. Gropman, David R. Adams, William A. Gahl, May Christine V. Malicdan, Cynthia J. Tifft, Lynne A. Wolfe, Paul R. Lee, John H. Postlethwait, Monte Westerfield, Anna Bican, Joy D. Cogan, Rizwan Hamid, John H. Newman, John A. Phillips, Amy K. Robertson
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
PurposeTo describe examples of missed pathogenic variants on whole-exome sequencing (WES) and the importance of deep phenotyping for further diagnostic testing.MethodsGuided by phenotypic information, three children with negative WES underwent target
Autor:
Patricia L. Weng, Keisha L. Gibson, Larry A. Greenbaum, Karan R. Kumar, Eileen D. Brewer, Tarak Srivastava, Michelle N. Rheault, Shashi K. Nagaraj, John W. Foreman, Jennifer D. Varner, Natasha Jawa, Eileen Tsai Chambers, Annabelle N. Chua, Delbert R. Wigfall, Cynthia Silva, Caroline Straatmann, David T. Selewski, John Barcia, T. Keefe Davis, Rachel M Engen, Christoph Licht, Jonathan H. Pelletier, Scott E. Wenderfer, Mahmoud Kallash, Rasheed Gbadegesin, Adam Bensimhon, Christoph P. Hornik
Publikováno v:
Pediatric Nephrology. 34:539-539
The original version of this article unfortunately contained a mistake. The subtitle “A Midwest Pediatric Nephrology Consortium (MWPNC) study” was missing. The correct title including subtitle is given above.
Autor:
Gaston Zilleruelo, Patrick D. Brophy, Vijay Kusnoor, Coral Hanevold, Bonita Falkner, Robert H. Mak, Johan Vande Walle, Michael Aigbe, Sándor Túri, Howard Trachtman, James A. Stewart, Donald L. Batisky, Randall Jenkins, Robert Achtel, Tivadar Tulassay, Melissa H Henshaw, Naomi Neufeld, Irene Restaino, Jeffery Blummer, Laszio Szabo, Jennifer Sugg, Jerilynn Radcliffe, Renli Teng, John Barcia, Robert Williams, Eva Marova, Joseph T. Flynn, David Headley, Ronald J. Portman, Juan C. Kupferman, Maria Horakova, Shashi K. Nagaraj, Ana Paredes, Kenneth A. Miller, Janice E. Sullivan, Lydia Hazan, Michael L. Moritz, William A. Primack, Joseph R. Sherbotie, Myra Chiang, Jonathan M. Sorof, L. Richard Feldenberg, Farahnak Assadi, Alexander Jurko, James W. Hainer
Publikováno v:
J Clin Hypertens (Greenwich)
This 4‐week randomized, double blind, placebo‐controlled study (N=240), 1‐year open label trial (N=233), and single‐dose pharmacokinetic study (N=22) evaluated candesartan cilexetil (3 doses) in hypertensive children aged 6 to 17 years. Seven