Confirmed Angiosarcoma: Prognostic Factors and Outcome in 50 Prospectively Followed Patients

Autor: N. J. Espat, J. J. Lewis, J. M. Woodruff, C. Antonescu, J. Xia, D. Leung, M. F. Brennan

Publikováno v: Sarcoma, Vol 4, Iss 4, Pp 173-177 (2000)

Purpose. Angiosarcoma is a rare tumor with endothelial cell differentiation that may arise in any anatomic location.The purpose of this report was to identify prognostic factors on outcome in a group of prospectively followed patients with confirm

Externí odkaz: https://doaj.org/article/c8890bd0f06a48f4be002f758fc79d15

Adrenocortical carcinoma

Autor: R D, Schulick, M F, Brennan

Publikováno v: World Journal of Urology. 17:26-34

Adrenocortical carcinoma is rare, tends to occur in the first decade as well as the fourth and fifth decades of life, and is slightly more common in women. The tumors are classified as functional or nonfunctional, depending on tumor production of cor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::518b69367e8c6d86a1fb71de4ba1ea5d
https://doi.org/10.1007/s003450050101

Irish Society of Gastroenterology

Autor: J. Coleman, D. Bouchier Hayes, M. A. Daw, R. O’More, C. T. Keane, C. O’Morain, G. W. Johnson, E. F. A. Spencer, A. J. Wilkinson, T. L. Kennedy, J. S. A. Collins, K. B. Bamford, B. J. Collins, J. M. Sloan, R. J. Moorehead, A. H. G. Love, C. McCarthy, R. Collins, S. Beattie, J. McDevitt, C. Feighery, C. O’Farrelly, D. G. Weir, D. Kelleher, A. Whelan, Y. Williams, D. Kellegher, D. Weir, M. C. Prabhakar, M. Daw, F. Keane, E. W. M. McDermott, B. Duduric, M. F. Brennan, R. Gaffney, J. O’Leary, T. Doyle, A. Gaffney, D. B. Gough, K. C. H. Fearon, P. Winstanley, D. C. Carter, O. J. McAnena, F. A. Moore, E. E. Moore, R. Pogetti, V. M. Peterson, C. M. Abemathy, P. Parsons, N. N. Williams, J. M. Daly, M. Herlyn, D. Bouchier-Hayes, N. F. Course, P. G. Horgan, A. Fahy, C. Delaney, J. M. Fitzpatrick, T. F. Gorey, S. Jazrawl, T. N. Walsh, P. J. Byrne, P. Lawlor, T. P. J. Hennessy, K. R. O’Sullivan, P. M. Mathias, M. McNicholas, M. Logan, J. Masterson, P. Gillen, J. Hyland, E. Beausang, W. P. Joyce, N. Williams, W. Maxwell, I. Reid, I. Sharpe, J. G. Geraghty, W. A. Tanner, S. Patchett, H. Mulcahy, N. Afdhal, D. O’Donoghue, A. Lohan, A. Darzi, F. B. V. Keane, P. W. N. Keeling, R. C. Gibney, R. Keane, J. Drumm, T. J. Egan, P. V. Delaney, G. O’Sullivan, P. Harte, P. A. Grace, A. Qureshi, H. Osbome, D. J. Bouchier-Hayes, S. L. Bamford, J. Geraghty, F. B. Keane, J. E. Coleman, A. Gleeson, K. Mealy, M. Barry, O. Traynor, J. J. Keating, A. Chua, S. Ah-Kion, J. McNulty, L. G. Heaney, P. Murphy, J. H. Connolly, M. E. Callender, P. MacMathuna, M. Farrant, D. O. B. Hourihane, P. Donaldson, M. Lombard, D. Westaby, Roger Williams, N. F. Couse, J. Burke, G. Lennon, C. P. Delaneyc, S. O’Brien, A. O’Brien, M. X. Fitzgerald, J. E. Hegarty, N. Noonan, M. Healy, R. O’Moore, O. I. Corrigan, P. W. N. Keating, H. U. I. Li, R. C. Stuart, S. Jazrawi, D. Wai, H. Jaeger, A. M. Jackson, C. J. Mitchell, J. MacFie, C. P. Delaney, K. McGeeney, M. T. P. Caldwell, D. P. O’Donoghue, J. Connolly, E. Kay, T. Gorey, P. McKiernan, J. F. T. Glasgow, B. T. Johnson, R. Ferguson, I. Davidson, J. Hurley, P. Keeling, T. Crowley, A. A. Long, D. P. O’Brien, R. P. Waldron, M. J. Shearer, H. F. Given, G. McEntee, J. Monson, J. Donohue, D. Nagomey, K. C. Trimble, A. M. Molloy, J. M. Scott, J. McKeever, T. P. J. Hennessey

Publikováno v: Irish Journal of Medical Science. 162:152-166

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7d24c44a7e556650e68ec63e163452bd
https://doi.org/10.1007/bf02942108

Confirmed angiosarcoma: prognostic factors and outcome in 50 prospectively followed patients

Autor: N J, Espat, J J, Lewis, J M, Woodruff, C, Antonescu, J, Xia, D, Leung, M F, Brennan

Publikováno v: Sarcoma

Purpose. Angiosarcoma is a rare tumor with endothelial cell differentiation that may arise in any anatomic location.The purpose of this report was to identify prognostic factors on outcome in a group of prospectively followed patients with confirmed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::62cacaaf02a32f301a2b2f1d18912790
https://pubmed.ncbi.nlm.nih.gov/18521298

Altered patterns of RB expression define groups of soft tissue sarcoma patients with distinct biological and clinical behavior

Autor: D, Polsky, S, Mastorides, D, Kim, M, Dudas, L, Leon, D, Leung, J M, Woodruff, M F, Brennan, I, Osman, C, Cordon-Cardo

Publikováno v: Histology and histopathology. 21(7)

Function of the retinoblastoma tumor suppressor protein (pRB) may be compromised at a genetic level by gene loss or mutation or at a post-translational level by hyperphosphorylation. In this study, we examined adult soft tissue sarcomas (ASTS) to det

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc11cb2b6cf4ef639e4e8c1214e4cd73
https://pubmed.ncbi.nlm.nih.gov/16598673