Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ian W Fellows"'
Autor:
Ian W Fellows, Helen Fellows
Publikováno v:
Medicine. 39:79-83
Anaemia is a common reason for referral to any gastroenterological service. Iron-deficiency anaemia is the most frequent, making up to 13% of referrals. The type of anaemia and any clinical symptoms often delineate the most appropriate investigations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3a3dce04bca129c596bc694602f79be
https://doi.org/10.1016/j.mpmed.2010.12.009
https://doi.org/10.1016/j.mpmed.2010.12.009
Publikováno v:
Blood Cells, Molecules, and Diseases. 23:288-291
ABSTRACT: We have examined normal individuals and all the patients currently being treated for hemochromatosis at the Norfolk and Norwich hospital for mutations in the HLA-H gene. We found a gene frequency in 200 normal subjects for the 845A (C282Y)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0848cf8e4666a0d6048fe901f1de57a3
https://doi.org/10.1006/bcmd.1997.0145
https://doi.org/10.1006/bcmd.1997.0145
Autor:
Vicky Bardsley, Jennie Z Wimperis, Gavin Willis, Barbara A. Jennings, Ray Lonsdale, Ian W Fellows
Publikováno v:
BMC Gastroenterology
BMC Gastroenterology, Vol 5, Iss 1, p 17 (2005)
BMC Gastroenterology, Vol 5, Iss 1, p 17 (2005)
Background Although most patients with hereditary haemochromatosis have HFE C282Y mutations, the lifetime risk to HFE C282Y homozygotes of developing fatal diseases such as hepatocellular carcinoma is uncertain. We have carried out a cross-sectional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851ec0d4f4c86a541b208f2caefa3027
https://pubmed.ncbi.nlm.nih.gov/15929796
https://pubmed.ncbi.nlm.nih.gov/15929796
Publikováno v:
Blood cells, moleculesdiseases. 31(2)
Most individuals diagnosed with hereditary hemochromatosis have mutations in both copies of the HFE gene, with such mutations being common in populations of north European origin. The number of individuals currently diagnosed and treated for hemochro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17009a4fde1a749940b7cc05c86be680
https://pubmed.ncbi.nlm.nih.gov/12972032
https://pubmed.ncbi.nlm.nih.gov/12972032
EDITOR—The conclusion of the letter by Allen and Williamson is based on speculation.1 They state that at least half of the individuals who are homozygous for the C282Y mutation of the HFE gene will develop symptoms and signs of haemochromatosis, bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f87174ab56f3c0e7e7393f2c0284504
https://europepmc.org/articles/PMC1127266/
https://europepmc.org/articles/PMC1127266/
Publikováno v:
Lancet (London, England). 354(9174)
Summary We found that C282Y homozygosity was not under-represented in an elderly male population. This suggests that life-threatening, haemochromatosis-related disease may not occur in many C282Y homozygotes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d01209272a7b4ec338cb9d1cf4d04284
https://pubmed.ncbi.nlm.nih.gov/10421310
https://pubmed.ncbi.nlm.nih.gov/10421310
Autor:
Andrew Yen, Megan Williams, Joseph D. Platko, Channing Der, Mark Hisaka, Alexander M. Feigin, C. Wang, C. D. Stiles, T. C. Cavalcanti, F. Guimaraesr, H. F. Gumerato, Q. S. Tahinc, Anita V. Ratnan, Hex Jby Su, Daniel D. Bxrle, Marc D. Basson, Fu Hong, Amalia Bianchi-Santamaria, Leonida Santamaria, Sergio Fedeli, A. Coral, P.A. Lamartiniere, B. C. Pence, M. J. Butler, D. M. Dunn, M. F. Miller, N. S. M. D. Wickramasinghe, H. Jo, J. M. McDonald, R. W. Hardy, G. Fernandes, B. Chandrasekar, J. T. Venkatraman, C. N. Kuratko, Mickie Bhatia, James B. Kirkland, Kelly A. Meckling-Gill, Nurul H. Sarkar, HuiWu Li, Wei Zhao, Trevor G. Atkinson, Danielle Martin, Helen de Salis, Christine Teixeira, Christine Pratt, A. A. Kulkarni, M. Sajan, K. Datta, P. Roy, A. P. Kulkarni, Rayudu Gopalakrishna, Zhen-hai Chen, Usha Gundimeda, S. J. Braunhut, D. Medeiros, M. R. Freeman, M. A. Moses, G. Y. Yang, A. M. Shamsuddin, Ivana Vucenik, Guang-Yu Yang, Abulkalam M. Shamsuddin, E. A. Paisley, James Kaput, H. J. Mangian, W. J. Visek, R. J. Hohl, K. Lewis, King-Thom Chung, Wen Chen, Yonggui Zhou, Peter P. Fu, Ronald W. Hart, Ming W. Chou, Valerian E. Kagan, Jack C. Yalowich, Julia Y. Tyurina, Vladimir A. Tyurin, V. B. Ritov, R. Goldman, D. A. Stoyanovsky, E. V. Menshikova, V. E. Kagan, Gerhard Zugmaier, Robert Jäger, Marco Gottardis, Klaus Havemann, Cornelius Knabbe, Ruth A. Hagerman, Susan M. Fischer, Mary F. Locniskar, H. S. Black, G. Okotie-Eboh, J. Gerguis, J. I. Urban, J. I. Thornby, H. Merrill, Leonard A. Sauer, Robert T. Dauchy, Jeanne M. Connolly, David P. Rose, H. L. Gensler, K. Gerrish, Y-M. Peng, M-J. Xu, Laura J. Jenski, Mustapha Zerouga, Lian Zhang, William Stillwell, P. Homayoun, M. K. Gupta, F. Lente, U. Tuason, T. Budd, M. Yazlovitskaya, George Melnykovych, Jenny A. Matthew, Steve Middleton, Alison Prior, Hugh J. Kennedy, Ian W. Fellows, Ian T. Johnson, Ping-Ping Lee, Margot M. Ip, C. Gercel-Taylor, D. D. Taylor, T. P. Pretlow, L. Hudson, M. A. O’Riordan, T. G. Pretlow, L. A. Cohen, E. Zang, A. Rivenson, Adria R. Sherman, Deborah Hrabinski, Vance Berger, Craig Dees, Don Henley, Murray Ardies, Curtis Travis, Doris M. Benbrook, Kevin Brewer, Coy Heldermon, Evelyn Nunez, Przemko Walisewaki, C. P. Reynolds, P. Einhorn, P. Schindler, J. J. Zuo, A. A. Khan, V. I. Avramis, J. G. Villablanca, D. P. Gaposchkin, S. A. Broitman, Singer C. Kosacoisky, M. Shlyankevich, R. Lee, K. Garden, Y.-C. Lee, Y.-J. Surh, Meena S. Katdare, Michael P. Osborne, Nitin T. Telang, Narayan Shivapurkar, Zhaocheng Tang, Oliver Alabaster, Jerzy A. Jaskeiwicz, Yu Zhao, Yoshiharu Shimomura, David W. Crabb, Robert A. Harris, Jan Zaleski, Patricia A. Richter, Gloria Y. Kwei, Frederick C. Kauffman, L. Hilakivi-Clarke, I. Onojafe, E. Cho, R. Clarke, M. E. Lippman
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781489909510
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b312403e0d86026b1b086f5702a8c41
https://doi.org/10.1007/978-1-4899-0949-7_14
https://doi.org/10.1007/978-1-4899-0949-7_14
Publikováno v:
EP Europace. 15:314-314
A 54-year-old woman underwent diagnostic ajmaline challenge as screening for Brugada syndrome. She received 1 mg/kg of ajmaline. The test was negative and there were no immediate complications. Three weeks later she developed pruritis, jaundice, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b663f0aaedb42900ee557755e3d095
https://doi.org/10.1093/europace/eus206
https://doi.org/10.1093/europace/eus206
Autor:
A.R. Davidson, M.W. Dronfield, A.M. Riordan, J. R. Crampton, S. Hishon, G. Neale, H.J. Kennedy, R. J. Dickinson, J. O. Hunter, R.E. Cowan, R.C.M. McGouran, G.N.W. Kerrigan, Ian W Fellows, J.H.B. Saunders
Publikováno v:
Lancet (London, England). 342(8880)
Elemental diet is as effective in producing remission of Crohn's disease (CD) as is corticosteroid treatment, but most patients relapse soon after resumption of a normal diet. We have investigated the efficacies of dietary modification and oral corti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82691d14fcc3374734830abd0a47c885
https://pubmed.ncbi.nlm.nih.gov/7903741
https://pubmed.ncbi.nlm.nih.gov/7903741