Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Sarah M. Moran"'
Autor:
Eleni Frangou, Annette Bruchfeld, Gema M. Fernandez-Juarez, Jürgen Floege, Dimitrios Goumenos, Sarah M. Moran, Stefanie Steiger, Kate I. Stevens, Kultigin Turkmen, Andreas Kronbichler
Publikováno v:
Počki, Vol 12, Iss 4, Pp 175-175 (2023)
No abstract
Externí odkaz:
https://doaj.org/article/cf4b30c185194b9fae88c0f3f547e889
Autor:
Shamma Al Nokhatha, Eithne Nic an Ríogh, Ted Fitzgerald, Cliona Cowhig, Louis Aslett, Arthur White, Matthew D. Griffin, Michael R. Clarkson, Alyssa Verrelli, Declan DeFreitas, Yvonne O’Meara, John Holian, Eamonn Molloy, Liam Casserly, Mark A. Little, Sarah M. Moran, Cathal Walsh, Julie Power, Jennifer Scott, Niall Conlon
Publikováno v:
HRB Open Research, Vol 5 (2022)
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a rare multisystem autoimmune disease. There is a need for interoperable national registries to enable reporting of real-world long-term outcomes and their predicto
Externí odkaz:
https://doaj.org/article/5feb6a7cd1fb43caacda30430c4c53c3
Autor:
Sarah M. Moran, Sean Barbour, Christine Dipchand, Jocelyn S. Garland, Michelle Hladunewich, Arenn Jauhal, Joanne E. Kappel, Adeera Levin, Sanjay Pandeya, Heather N. Reich, Susan Thanabalasingam, Dorothy Thomas, Jeffrey C. Ma, Christine White
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Purpose of program: This article will provide guidance on how to best manage patients with glomerulonephritis (GN) during the COVID-19 pandemic. Sources of information: We reviewed relevant published literature, program-specific documents, and guidan
Externí odkaz:
https://doaj.org/article/13af96c33d0041a392519d7e772c0f9c
Autor:
Christine A. White, Joanne E. Kappel, Adeera Levin, Sarah M. Moran, Sanjay Pandeya, Susan J. Thanabalasingam
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 7 (2020)
Purpose of program: To provide guidance on the management of patients with advanced chronic kidney disease (CKD) not requiring kidney replacement therapy during the COVID-19 pandemic. Sources of information: Program-specific documents, pre-existing,
Externí odkaz:
https://doaj.org/article/b1769599003f4757addbe9c55d95739f
Autor:
Niall Conlon, Elizabeth Groarke, John Holian, Tomás P. Griffin, Matthias Kretzler, Mark A. Little, Paul V. O’Hara, Kirsty McLoughlin, Matthew D. Griffin, Michael R. Clarkson, Conor Judge, Jason Wyse, Jennifer Scott, Sarah M Moran, Jean Dunne
Publikováno v:
J Am Soc Nephrol
Background Up to 70% of patients with ANCA-associated vasculitis (AAV) develop GN, with 26% progressing to ESKD. Diagnostic-grade and noninvasive tools to detect active renal inflammation are needed. Urinary soluble CD163 (usCD163) is a promising bio
Publikováno v:
Clin J Am Soc Nephrol
Kidney homeostasis is highly dependent upon the correct functioning of myeloid cells. These cells form a distributed surveillance network throughout the kidney, where they play an integral role in the response to organ threat. Dysregulation of reside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03ea67d1cabbb504e7dc54a8120fd0f0
https://europepmc.org/articles/PMC8823925/
https://europepmc.org/articles/PMC8823925/
Autor:
Jennifer Scott, Eithne Nic an Ríogh, Shamma Al Nokhatha, Cliona Cowhig, Alyssa Verrelli, Ted Fitzgerald, Arthur White, Cathal Walsh, Louis Aslett, Declan DeFreitas, Michael R. Clarkson, John Holian, Matthew D. Griffin, Niall Conlon, Yvonne O’Meara, Liam Casserly, Eamonn Molloy, Julie Power, Sarah M. Moran, Mark A. Little
Publikováno v:
HRB Open Research. 5:80
Background: Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a rare multisystem autoimmune disease. There is a need for interoperable national registries to enable reporting of real-world long-term outcomes and their predicto
Autor:
Michael J. Rauh, Matthew B. Lanktree, Caitlyn Vlasschaert, Kestenbaum B, Robinson-Cohen C, Sarah M Moran, Wilma M. Hopman, McNaughton Ajm, Rachel M. Holden, Jocelyn S. Garland
BackgroundClonal hematopoiesis of indeterminate potential (CHIP) is an inflammatory premalignant disorder resulting from acquired genetic mutations in hematopoietic stem cells. CHIP is common in aging populations and associated with cardiovascular mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d14e2a6f67cbfd70399ee59c78b5d1a
https://doi.org/10.1101/2021.06.30.21259343
https://doi.org/10.1101/2021.06.30.21259343
Autor:
Caitlyn Vlasschaert, Amy J.M. McNaughton, Michael Chong, Elina K. Cook, Wilma Hopman, Bryan Kestenbaum, Cassianne Robinson-Cohen, Jocelyn Garland, Sarah M. Moran, Guillaume Paré, Catherine M. Clase, Mila Tang, Adeera Levin, Rachel Holden, Michael J. Rauh, Matthew B. Lanktree
Publikováno v:
J Am Soc Nephrol
Clonal hematopoiesis of indeterminate potential (CHIP) is an inflammatory premalignant disorder resulting from acquired genetic mutations in hematopoietic stem cells. This condition is common in aging populations and associated with cardiovascular mo
Autor:
Sarah M Moran, Gerjan J. Dekkema, Coen A. Stegeman, Theo Bijma, Jan-Stephan F. Sanders, Mark A. Little, Louise Ryan, Wayel H. Abdulahad, Peter Heeringa
Publikováno v:
Nephrology, Dialysis, Transplantation, 34(2), 234-242. Oxford University Press
Nephrology Dialysis Transplantation
Nephrology Dialysis Transplantation
Background. Early detection of renal involvement in anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) is of major clinical importance to allow prompt initiation of treatment and limit renal damage. Urinary soluble cluster of