Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kerri Gallagher"'
Autor:
Paul Edgar Gray, Bella Shadur, Susan Russell, Richard Mitchell, Michael Buckley, Kerri Gallagher, Ian Andrews, Kevin Thia, Joseph A. Trapani, Edwin Philip Kirk, Ilia Voskoboinik
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Bi-allelic null mutations affecting UNC13D, STXBP2, or STX11 result in defects of lymphocyte cytotoxic degranulation and commonly cause familial hemophagocytic lymphohistiocytosis (FHL) in early life. Patients with partial loss of function are increa
Externí odkaz:
https://doaj.org/article/9b1fec07a2704ab881fd21c60040f714
Autor:
Nicholas Ho, Judith M. Spies, Kerri Gallagher, Heidi N. Beadnall, Benjamin P. Trewin, Stephen Adelstein, Michael Barnett, Joshua Barton
Publikováno v:
Multiple Sclerosis and Related Disorders. 43:102175
Background B-cell depleting treatments are widely used to modify the course of neuromyelitis optica spectrum disorder (NMOSD). Despite recent successful Phase 3 trials of several novel NMOSD therapies, limited availability and high cost constrains th
Autor:
Kerri Gallagher, Ilia Voskoboinik, Richard Mitchell, Pamela Palasanthiran, Paul Gray, Kevin Y. T. Thia, Bella Shadur, Susan Russell
Publikováno v:
Journal of the Pediatric Infectious Diseases Society. 8(1)
Single gene defects that impair lymphocyte cytotoxicity can predispose to severe viral infection that normally remains subclinical. The classic severe presentation is hemophagocytic lymphohistiocytosis. Here, we report the case of a neonate who prese
Autor:
Ilia Voskoboinik, Susan Russell, Michael F. Buckley, Edwin P. Kirk, Paul Gray, Kevin Y. T. Thia, Bella Shadur, Joseph A. Trapani, Kerri Gallagher, Richard Mitchell, Ian Andrews
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 8 (2017)
Frontiers in Immunology, Vol 8 (2017)
Bi-allelic null mutations affecting UNC13D, STXBP2 or STX11 result in defects of lymphocyte cytotoxic degranulation, and commonly cause familial haemophagocytic lymphohistiocytosis (FHL) in early life. Patients with partial loss of function are incre
Publikováno v:
Pathology. 51:S131
Autor:
Kerri Gallagher, Bonnie Hiener, Catriona M. McNeil, Sarah Palmer, Ajantha Solomon, Sharon R Lewin, Roger Garsia, Fiona Wightman, Nicolás Urriola, Sanjeev Kumar
Publikováno v:
AIDS. 29:504-506
Long-lived latently infected resting CD4+ T cells are the main reason why current antiretroviral therapy (ART) is unable to cure HIV infection [1]. Recent work has suggested that the expression of immune checkpoint markers, such as programmed death-1
Autor:
Kerri Gallagher, Stephen Adelstein, Andrew Williams, Watson W. S. Ng, Dana Bird, Vicky Wong, Kara Smithers, Tri Giang Phan
Publikováno v:
Clinical Diagnostic Laboratory Immunology. 8:471-474
We evaluated methods for the detection of autoantibodies to extractable nuclear antigens (ENAs) to determine the strategy that yielded the most cost effective and clinically meaningful result. We prospectively compared counterimmunoelectrophoresis (C
Autor:
Matthew C. Cook, David A. Fulcher, Stephen Adelstein, Theo Demalmanche, Dan Suan, Gary Chew, Sharon Choo, Pravin Hissaria, Kerri Gallagher, Sue Wong, Joy Mundy, Chris Czajko, Louise Wienholt, Elizabeth Moore, Karla Lemmert
Publikováno v:
Pathology. 43:S41-S42
Common variable immunodeficiency (CVID) is a heterogeneous B-cell immunodeficiency disorder often characterised by failure of memory B-cell development and antibody secretion. Attempts have been made to stratify patients into clinical subsets based o
Autor:
William J. Maskill, Kerri Gallagher, Ian D. Gust, Kevin A. Rickard, D. F. Kenny, Antony Basten, Roger Garsia, P. A. Gatenby
Publikováno v:
Australian and New Zealand Journal of Medicine. 17:371-378
One hundred and sixty-one Australian patients with hereditary bleeding disorders comprising hemophilia A (120), hemophilia B (18), von Willebrand's disease (16), and seven symptomatic female hemophilia A or B carriers were screened for clinical and s
Autor:
Paul A. Gatenby, Kerri Gallagher, Henry M. Kronenberg, Douglas E. Joshua, Antony Basten, Kaye Cameron, John Gibson
Publikováno v:
Australian and New Zealand journal of medicine. 18(7)