Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Debra Canter"'
Autor:
Kabita Nanda, Melissa E. Elder, Susan Nielsen, Kathleen M. O'Neil, Joanna M. Lubieniecka, Dawn M. Wahezi, Andreas Reiff, Erica F. Lawson, Gloria C. Higgins, Kimberly Morishita, Jennifer E. Weiss, Susan Kim, Andrew J. White, Debra Canter, Goran Ristic, Susanne M. Benseler, Deborah McCurdy, Mikhail Kostik, Mary B. Toth, Linda Wagner-Weiner, David A. Cabral, Lakshmi N. Moorthy, Aimee O. Hersh, Marisa S. Klein-Gitelman, Susan Shenoi, Eyal Muscal, Barbara A. Eberhard, Sarah Campillo, Angelyne Sarmiento, Tzielan Lee, Angela Byun Robinson, Heather Van Mater, Adam M. Huber, Marinka Twilt, Raju Khubchandani, Rae S. M. Yeung, Steven J. Spalding, Sirirat Charuvanij, Paul Dancey
Publikováno v:
Arthritis & Rheumatology. 68:2514-2526
Objective To uniquely classify children with microscopic polyangiitis (MPA), to describe their demographic characteristics, presenting clinical features, and initial treatments in comparison to patients with granulomatosis with polyangiitis (Wegener'
Publikováno v:
Hospital Pediatrics. 6:496-500
BACKGROUND: Diffuse alveolar hemorrhage (DAH) is a devastating clinical syndrome characterized by a falling hematocrit, respiratory insufficiency, and radiographic evidence of pulmonary infiltrates. Literature regarding management of DAH in childhood
Autor:
Debra Canter, Adisak Suwanichkul, Alvaro Orjuela, Scott E. Wenderfer, M. John Hicks, Sridevi Devaraj, Eyal Muscal, Charles G. Minard
Publikováno v:
American Journal of Nephrology. 41:241-247
Background/Aims: There is a critical need for more noninvasive biomarkers to identify nephritis in patients with systemic lupus erythematosus (SLE). Recent studies in a model mouse and an adult SLE patient cohort suggest that anti-basement membrane a
Autor:
Mohammad K. Eldomery, Olaug K. Rødningen, Cecilia Poli, Debra Canter, Berit Flatø, Ketil Heimdal, Nicholas L. Rider, Silje F. Jørgensen, Hasibe Artac, Hans Christian Erichsen, Francisco Javier Espinosa Rosales, Ivan K. Chinn, Alison A. Bertuch, Bo Yuan, Jordan S. Orange, Emily M. Mace, Wojciech Wiszniewski, Robert Lyle, Shalini N. Jhangiani, Tobias Gedde-Dahl, Carla M. Davis, Carl E. Allen, I. Celine Hanson, Magnus K. O. Burstedt, Thomas B. Issekutz, Mari Ann Kulseth, Yavuz Bayram, Eric A. Smith, Tram N. Cao, Stephen Jolles, Andrew C. Issekutz, Pubudu S. Samarakoon, Alice Y. Chan, Gozde Yesil, Eva Holmberg, Børre Fevang, Diana K. Bayer, John W. Belmont, Asbjørg Stray-Pedersen, Timothy J. Vece, Magdalena Walkiewicz, James R. Lupski, Ying Sheng, Trine Prescott, Liv T. N. Osnes, Cecilie F. Rustad, Nina Denisse Guerrero-Cursaru, Juan Carlos Aldave Becerra, Victor Wei Zhang, Philip M. Boone, Mohammad S. Ehlayel, Jason W. Caldwell, Tore G. Abrahamsen, José Luis Franco, Harshal Abhyankar, Henrik Hjorth-Hansen, Liliana Bezrodnik, Vegard Skogen, Nicola A.M. Wright, Lisa R. Forbes, Anne Grete Bechensteen, Christine R. Beck, Saul Oswaldo Lugo Reyes, Lee-Jun C. Wong, Shen Gu, Sarah K. Nicholas, Christina E. West, Filiz O. Seeborg, Mehmed M. Atik, Eric Boerwinkle, Luis A. Pedroza, Caterina Cancrini, Hanne Sørmo Sorte, Yaping Yang, Christine M. Eng, Richard A. Gibbs, Lenora M. Noroski, Alessandro Aiuti, Ender Karaca, Torstein Øverland, Claudia Milena Trujillo Vargas, Jordan K. Abbott, Geir E. Tjønnfjord, William T. Shearer, Javier Chinen, Ingunn Dybedal, Tomasz Gambin, Donna M. Muzny, Pål Aukrust, Ingvild Nordøy, María Soledad Caldirola, Jianhong Hu, Zeynep Coban Akdemir
Publikováno v:
The Journal of allergy and clinical immunology, vol 139, iss 1
WOS: 000393996800025
PubMed: 27577878
Background: Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous disorders thus far associated with mutations in more than 300 genes. The clinical phenotypes derived fr
PubMed: 27577878
Background: Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous disorders thus far associated with mutations in more than 300 genes. The clinical phenotypes derived fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2abf0338cd9012533e4851a811cd28aa
https://escholarship.org/uc/item/8188960d
https://escholarship.org/uc/item/8188960d
Autor:
Marietta De Guzman, Angelo P. Giardino, Debra Canter, Jeannine Yoon, Patricia Rosillo, Eyal Muscal
Publikováno v:
Pediatric Dimensions. 1
Autor:
Levi B. Watkin, Marietta M. de Guzman, Scott D. McKinley, Karen W. Eldin, Timothy J. Vece, Lisa R. Forbes, Jordan S. Orange, Robert Paul Guillerman, Ivan K. Chinn, Michael C. Braun, Debra Canter, Grant Bertolet, Sarah K. Nicholas
Publikováno v:
Journal of clinical immunology. 36(4)
Inherently defective immunity typically results in either ineffective host defense, immune regulation, or both. As a category of primary immunodeficiency diseases, those that impair immune regulation can lead to autoimmunity and/or autoinflammation.
Autor:
Isabella Quinti, Damiano Abeni, Stefano Tabolli, Debra Canter, Patrizia Giannantoni, Joud Hajjar, Federica Pulvirenti, Cinzia Milito, Jordan S. Orange
Publikováno v:
The journal of allergy and clinical immunology. In practice. 4(6)
Background Generic health status quality of life (QoL) instruments have been used in patients with common variable immune deficiency (CVID). However, by their nature, these tools may over- or underestimate the impact of diseases on an individual's Qo
Autor:
Sara K Sexson Tejtel, Andrea A Ramirez, Amy Liou, Thomas Seery, Debra Canter, Marietta DeGuzman, Carolyn Altman
Publikováno v:
Circulation. 131
Background: Kawasaki disease is the leading cause of acquired heart disease in children in the US. While it remains a rare disease, the purpose of this study is to evaluate the incidence of KD Methods: To evaluate our hypothesis we used the Pediatric
Autor:
Thomas J. Seery, Sara K Sexson Tejtel, Amy Liou, Caroly A Altman, Debra Canter, Marietta DeGuzman, Andrea A Ramirez
Publikováno v:
Circulation. 131
Kawasaki disease (KD) is the leading cause of acquired heart disease in children with a subset presenting in shock. We sought to describe the incidence and outcomes of KD shock in the US. Methods: The Pediatric Health Information Systems (PHIS), 1/20
Autor:
Asbjørg Stray-Pedersen, Levi B. Watkin, Debra Canter, Sharon D. Dell, N. Tony Eissa, Claudia Gonzaga-Jauregui, John Hicks, Mickie H. Cheng, Dongfang Liu, Eric Boerwinkle, Noah Zaitlen, Feroz R. Papa, Kirk D. Jones, Emily M. Mace, Pui-Yan Kwok, Michael Waterfield, Birthe Jessen, Wojciech Wiszniewski, Timothy J. Vece, Sarah K. Nicholas, Ling Fung Tang, Suzanne M. Leal, Mark S. Anderson, Regie Lyn P. Santos-Cortez, Kwanghyuk Lee, James R. Lupski, Michael Rosenblum, Jordan S. Orange, George Makedonas, Shalini N. Jhangiani, Christopher S. Law, Samantha Penney, Richard A. Gibbs, Karen Nahmod, Max Jan, Youbao Sha, Lisa R. Forbes, Tomasz Gambin, Anthony K. Shum, Donna M. Muzny, Maike Thamsen
Publikováno v:
Nature genetics, vol 47, iss 6
Advances in genomics have allowed unbiased genetic studies of human disease with unexpected insights into the molecular mechanisms of cellular immunity and autoimmunity1. We performed whole exome sequencing (WES) and targeted sequencing in patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d083805f033f211e5f9deafbb44d842
https://europepmc.org/articles/PMC4513663/
https://europepmc.org/articles/PMC4513663/