Zobrazeno 1 - 10
of 205
pro vyhledávání: '"L W Powell"'
Autor:
Yves Deugnier, Louise E. Ramm, D. Jeannette, C. Andrew, L. W. Powell, M. Emilie, M. Jeff, T. Bruno, Grant A. Ramm, A. Gregory, Laine Fabrice, Edouard Bardou-Jacquet
Publikováno v:
Journal of Hepatology. 68:S419
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dc2bb15deb95ecfe2c520f290a48fde
https://doi.org/10.1016/s0168-8278(18)31078-x
https://doi.org/10.1016/s0168-8278(18)31078-x
Autor:
Katrina J. Allen, Dallas R. English, Graham G. Giles, Christine E. McLaren, Nicholas J. Osborne, John L. Hopper, Lyle C. Gurrin, Martin B. Delatycki, Gregory J. Anderson, C.C. Constantine, Melissa C. Southey, L. W. Powell, Dorota M. Gertig, John K. Olynyk
Publikováno v:
Gastroenterology. 135:1945-1952
Background & Aims There are few longitudinal studies of serum ferritin (SF) and transferrin saturation (TS) levels in individuals homozygous for the C282Y mutation. We characterized the development of elevated iron measures in C282Y homozygotes follo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7ce3a2f35fe8453da80c82f8a8f9f9a
https://doi.org/10.1053/j.gastro.2008.08.056
https://doi.org/10.1053/j.gastro.2008.08.056
SummarySummary: In the treatment of peptic ulcer, antacids should only be used when required for pain relief; for this purpose, any of the relatively non-“potent” antacids such as tablet preparations appear adequate. Antacids containing calcium c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef64f04f57ecba601d744632172f05a6
https://doi.org/10.1159/000391665
https://doi.org/10.1159/000391665
Autor:
David M. Frazer, Darrell H. G. Crawford, K N Millard, L. W. Powell, Sarah J. Wilkins, Jeannette L. Dixon, Gregory J. Anderson, Kim R. Bridle, Grant A. Ramm, V.N. Subramaniam
Publikováno v:
Journal of Gastroenterology and Hepatology. 18:B59-B90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b00dd0c9328646bc88663fe7e8c868
https://doi.org/10.1046/j.1440-1746.18.s2.5.x
https://doi.org/10.1046/j.1440-1746.18.s2.5.x
Autor:
M Johnson, F Cordingley, Darrell H. G. Crawford, Peter E. Hickman, W Ferguson, L F Hourigan, J Shaw, L. W. Powell, K McDonell, Goce Dimeski, J Ascough, B Ormiston, A Pink
Publikováno v:
Gut. 46:405-409
BACKGROUND—C282Y hereditary haemochromatosis is an appropriate condition for population screening. Transferrin saturation, the best screening test to date, is relatively expensive, labour intensive, and cannot be automated. Unsaturated iron binding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::608c1ebe858cf4bfe771570bf4050ed1
https://doi.org/10.1136/gut.46.3.405
https://doi.org/10.1136/gut.46.3.405
Autor:
L W, Powell, T R, Yapp
Publikováno v:
Clinics in Liver Disease. 4:211-228
The recent cloning of the hemochromatosis gene (HFE) and the demonstration that a single missense mutation is responsible for 90% or more of patients with the disease, have stimulated renewed interest in all aspects of this common disease. The molecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d5a51ba4256463c5d85c7faca3f089
https://doi.org/10.1016/s1089-3261(05)70104-5
https://doi.org/10.1016/s1089-3261(05)70104-5
Autor:
James C. Barton, Christine E. McLaren, Gregory J. Anderson, Lyle C. Gurrin, Mary J. Emond, V. N. Subramaniam, L. W. Powell, Gordon D. McLaren, Pradyumna D. Phatak, Paul C. Adams, Grant A. Ramm
Publikováno v:
Hepatology. 62:1918-1919
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6bea6b877a8cc95312fb1966a543d03
https://doi.org/10.1002/hep.27851
https://doi.org/10.1002/hep.27851
Autor:
L W Powell, D K George
Publikováno v:
Alimentary Pharmacology and Therapeutics. 11:631-639
Haemochromatosis was first recognized as a disease entity over a century ago and its hereditary nature recognized over 60 years ago. However it was only in late 1996 that the haemochromatosis gene was cloned and a single C282Y mutation confirmed as b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a61f6d7e6d1bfe2389901465c224019
https://doi.org/10.1046/j.1365-2036.1997.00197.x
https://doi.org/10.1046/j.1365-2036.1997.00197.x
Autor:
J.L. Dixon, L. W. Powell, Daniel F. Wallace, L. Summerville, Katherine E. Arden, Gregory J. Anderson, Grant A. Ramm, V.N. Subramaniam, Jeffrey Searle
Publikováno v:
ResearcherID
Background: A severe form of iron overload with the clinicopathological features of haemochromatosis inherited in an autosomal dominant manner has been described in the Solomon Islands. The genetic basis of the disorder has not been identified. The d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af228cea37d7d2e5070da902eb4cef21
https://doi.org/10.1136/gut.52.8.1215
https://doi.org/10.1136/gut.52.8.1215
Autor:
Peter Malfertheiner, Paul C. Adams, Antonello Pietrangelo, N. Lynch, Louis Griffel, Pradyumna D. Phatak, Claus Niederau, J. Gross, L. W. Powell, Wolfgang Stremmel, Alberto Piperno, Herbert L. Bonkovsky, U. Stoelzel, Y. Zhang, Mark W. Russo, M. Wurster, Gordon D. McLaren, Pierre Brissot
Background and Aims: Hereditary hemochromatosis (HH) is characterized by increased intestinal iron absorption. Consequences of iron overload include organ dysfunction, cirrhosis and hepatocellular carcinoma. Although phlebotomy is the standard of car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd05e3e43edd0772cf43996ef1820f2f