Zobrazeno 1 - 10
of 52
pro vyhledávání: '"B.M. McFarlane"'
Autor:
M. G. Saleh, I.G. McFarlane, Leila Maria Moreira Beltrão Pereira, B.M. McFarlane, Sérgio Mies, C. Bridger, P. Massarolo, Victorino Spinelli
Publikováno v:
Transactions of the Royal Society of Tropical Medicine and Hygiene. 91:310-314
To investigate the possible involvement of autoimmune mechanisms in the development of hepatosplenic schistosomiasis (HSS), 234 patients with chronic Schistosoma mansoni infections were screened for a wide range of non-organ-specific autoantibodies a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c23ee34bdd7485ea9a94b868cd717a5a
https://doi.org/10.1016/s0035-9203(97)90088-2
https://doi.org/10.1016/s0035-9203(97)90088-2
Autor:
A. Boschi, I.G. McFarlane, Luciano Attard, Roger Williams, Cynthia Bridger, B.M. McFarlane, M. G. Saleh, Gabriella Verucchi, Francesco Chiodo, Antonella Fuzio, Christopher J. Tibbs
Publikováno v:
Journal of Medical Virology. 42:66-72
Serial serum samples from 16 Italian patients presenting with acute hepatitis C virus (HCV) infections (which progressed to chronic hepatitis in six) were screened for the non-organ-specific autoantibodies most frequently associated with autoimmune h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae9a0fe4947dbe3b80c2bf8df2e31980
https://doi.org/10.1002/jmv.1890420113
https://doi.org/10.1002/jmv.1890420113
Publikováno v:
Journal of Gastroenterology and Hepatology. 5:244-251
In patients with chronic active hepatitis (CAH), the absence of the conventional serum auto-antibodies (antinuclear, smooth muscle and liver-kidney microsomal) is often taken as evidence against an auto-immune aetiology and as indicative that the dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35ec203e4b44b3e0310d9d217bd6c89a
https://doi.org/10.1111/j.1440-1746.1990.tb01624.x
https://doi.org/10.1111/j.1440-1746.1990.tb01624.x
Publikováno v:
Hepatology. 11:408-415
Autoantibodies reacting with the galactose-specific hepatic asialoglycoprotein receptor—a liver-specific component expressed on the surfaces of hepatocytes—are often found in patients with chronic active hepatitis of presumed autoimmune origin. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6fea575ad2d7cc51fa1a022ba435a42
https://doi.org/10.1002/hep.1840110312
https://doi.org/10.1002/hep.1840110312
Publikováno v:
Autoimmunity. 35(8)
No longitudinal study has investigated whether autoantibody titres and serum IgG levels correlate with disease activity in autoimmune liver disease. To determine this, we investigated prospectively 19 patients on 254 occasions between 10 months to 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee00494d9c4771bb592e9d1976313d4b
https://pubmed.ncbi.nlm.nih.gov/12765477
https://pubmed.ncbi.nlm.nih.gov/12765477
Autor:
T. I. Michalak, Joseph Lau, GraemeJ.M. Alexander, Roger Williams, A. L. W. F. Eddleston, B.M. McFarlane
Publikováno v:
Scopus-Elsevier
SUMMARY The susceptibility of hepatocytes from patients with chronic hepatitis B to complement-dependent cytotoxicity mediated by heterologous antibodies to hepatitis B virus core (anti-HBc) and surface (anti-HBc) antigens and to hepatic asialoglycop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbe770fd665c8e9f395822eb2f191575
https://europepmc.org/articles/PMC1534334/
https://europepmc.org/articles/PMC1534334/
Autor:
B.M. McFarlane, John Koskinas, Peter T. Donaldson, Ian G. McFarlane, Christopher J. Tibbs, Masashi Mizokami, Roger Williams, Kayhan T. Nouri-Aria
Publikováno v:
Gastroenterology. 107(5)
Background/Aims: Previous reports have suggested that the hepatitis C virus (HCV) may induce autoimmune hepatitis. The aim of this study was to examine this hypothesis by investigating humoral and cellular immune responses to HCV-related antigens and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cfc39cabbc54eab6806d770c9b94915
https://pubmed.ncbi.nlm.nih.gov/7523229
https://pubmed.ncbi.nlm.nih.gov/7523229
Publikováno v:
Journal of hepatology. 21(5)
Recent work has shown that there is antigenic similarity between common bacterial proteins and epitopes on biliary epithelial cells. Following evidence that the sera of all of a series of patients with primary biliary cirrhosis contained antibodies t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c3a29bf4451ad6dabf5f1faad4770ac
https://pubmed.ncbi.nlm.nih.gov/7890908
https://pubmed.ncbi.nlm.nih.gov/7890908
Autor:
B.M. McFarlane, Freni Ma, Felix Stickel, G. Gerken, Ian G. McFarlane, Karl-Hermann Meyer zum Büschenfelde, Kendo Kiyosawa, Edward L. Krawitt, Ulrich Treichel, Nuntiata Alessi, Takeshi Seki, Seichi Furuta
Publikováno v:
Gastroenterology. 107(3)
The asialoglycoprotein receptor (ASGPR) is an established, liver-specific autoantigen. This multicenter study investigated the specificity of anti-ASGPR autoantibodies for autoimmune hepatitis (AIH) in different ethnic groups.Nine hundred fourteen se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33cd0ee035ea15d26400665c88a69f41
https://pubmed.ncbi.nlm.nih.gov/8076767
https://pubmed.ncbi.nlm.nih.gov/8076767
Antibodies to hepatitis C virus in autoimmune liver disease: evidence for geographical heterogeneity
Autor:
Philip J. Johnson, Giorgio Ballardini, Heather M. Smith, Roger Williams, B.M. McFarlane, I.G. McFarlane, F.B. Bianchi, C. Bridger, Diego Vergani, M. Lenzi
Publikováno v:
Lancet (London, England). 338(8762)
To resolve conflicting reports about the occurrence of antibodies against hepatitis C virus (HCV) in patients with autoimmune chronic active hepatitis (AI-CAH), sera from UK and Italian patients were tested with the original anti-HCV assay (Ortho) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d48a9c3ad1ad7d31f98bb8dc511bf6b
https://pubmed.ncbi.nlm.nih.gov/1677111
https://pubmed.ncbi.nlm.nih.gov/1677111