Studies on the preparation and rearrangement of certain steroid oxides

Autor: E M, HICKS, C J, BERG, E S, WALLIS

Publikováno v: The Journal of biological chemistry. 162

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9ea61973061691d135796707d0ce9b7e
https://pubmed.ncbi.nlm.nih.gov/21018772

Mammary tumor formation in p53- and BRCA1-deficient mice

Autor: V L, Cressman, D C, Backlund, E M, Hicks, L C, Gowen, V, Godfrey, B H, Koller

Publikováno v: Cell growthdifferentiation : the molecular biology journal of the American Association for Cancer Research. 10(1)

The inheritance of a mutant copy of the BRCA1 gene greatly increases a woman's lifetime risk for ovarian and breast cancer. While a homologous gene has been identified in mouse, mice carrying mutations in this gene do not display a detectable increas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4d09a59590d93e34b500a7b7d7749531
https://pubmed.ncbi.nlm.nih.gov/9950212

Progressive neuronal degeneration of childhood (Alpers syndrome) with hepatic cirrhosis

Autor: D. McGibben, E. M. Hicks, I. V. Allen, D. C. Wilson

Publikováno v: European journal of pediatrics. 152(3)

Four children, from two families, suffered from fatal degeneration of the cerebral grey matter. Their disease was characterised by intractable epilepsy, epilepsia partialis continua, progressive deterioration, and terminal hepatic dysfunction. EEG sh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c9882ebf854f5dfdae97b78b1f068b3
https://pubmed.ncbi.nlm.nih.gov/8444257

Proceedings of the ulster paediatric society and irish paediatric association, joint clinical meeting; 5th — 7th may, 1989

Autor: P. Higgins, C. Boreham, S. Cullen, C. M. Hill, A. Sloane, V. E. Boston, C. McKenna, Emma Curtis, A. Kurien, D. Duff, Fitzgerald Rj, S. Brown, M. Tsuji, I. J. Temperlery, M. A. Avaria, T. C. Taylor, Mark Lawler, N. O’Brien, Hilary Hoey, B. Denham, I. V. Allen, E. Hicks, T. J. Flood, T. R. J. Tubman, Ronnie Moore, Michael D. Shields, H. C. Mulholland, G. P. P. Fox, JM Savage, C. Norse, C. Fitzpatrick, O. Conor Ward, P. Greally, D. C. Wilson, E. Tempany, J. Jenkins, F. Breatnach, Ann M. Bergin, P. H. Robinson, D. A. Brown, D. McGibben, N. V. O’Donohoe, Hugh Monaghan, N. C. Rollins, J. Lim, Brian Denham, J. F. T. Glasgow, D. Primrose, H. Monaghan, D. J. Reena, J. Crane, E. A. Magill, O. Hensey, N. Anderson, D. C. Carson, J. B. G. Watson, Anthony Staines, S. R. McCann, B. O’Shea, El Hussein Rfidah, P. Cervi, M. D. Rollins, R. J. Stewart, A. Maguire, J. F. Jackson, J. McMenamin, B. Craig, M. D. O’Hara, G. McClure, A. O’Meara, E. Conneally, E. Fitzgerald, G. Murray, Peter Humphries, T. G. Mathews, B. Connolly, M. Tynan, J. McAloon, O. C. Ward, Mary D. King, P. Crean, J. Hankins, Angela H. Bell, J. Hurley, Mc Creid, E. M. Hicks, Denis Gill, F. McManus, V. H. Patterson, S. Sallan, I. J. C. Wallace

Publikováno v: Irish Journal of Medical Science. 158:284-290

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ac97623612838e6b8f83292e844203e
https://doi.org/10.1007/bf02942073

Reye's syndrome

Autor: J F, Glasgow, E M, Hicks, J G, Jenkins, S R, Keilty, G W, Black, T F, Fannin

Publikováno v: British journal of hospital medicine. 34(1)

Reye's syndrome, an uncommon childhood encephalopathy of uncertain aetiology, is an important cause of mortality and permanent handicap. Since its recognition treatment has changed, current management focusing upon prevention or control of raised int

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6f455dc17c0c2ea1d0165c5ef62f24c1
https://pubmed.ncbi.nlm.nih.gov/4016409