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Journal Abstract Search
143 related items for PubMed ID: 3191501
1. Phase I trial and clinical pharmacological evaluation of hexamethylene bisacetamide administration by ten-day continuous intravenous infusion at twenty-eight-day intervals. Young CW, Fanucchi MP, Declan Walsh T, Baltzer L, Yaldaei S, Stevens YW, Gordon C, Tong W, Rifkind RA, Marks PA. Cancer Res; 1988 Dec 15; 48(24 Pt 1):7304-9. PubMed ID: 3191501 [Abstract] [Full Text] [Related]
2. Phase I clinical and pharmacokinetic study of hexamethylene bisacetamide (NSC 95580) administered as a five-day continuous infusion. Egorin MJ, Sigman LM, Van Echo DA, Forrest A, Whitacre MY, Aisner J. Cancer Res; 1987 Jan 15; 47(2):617-23. PubMed ID: 3791246 [Abstract] [Full Text] [Related]
3. Prolonged infusion of hexamethylene bisacetamide: a phase I and pharmacological study. Rowinsky EK, Ettinger DS, McGuire WP, Noe DA, Grochow LB, Donehower RC. Cancer Res; 1987 Nov 01; 47(21):5788-95. PubMed ID: 3664482 [Abstract] [Full Text] [Related]
4. Phase I bioavailability and pharmacokinetic study of hexamethylene bisacetamide (NSC 95580) administered via nasogastric tube. Ward FT, Kelley JA, Roth JS, Lombardo FA, Weiss RB, Leyland-Jones B, Chun HG. Cancer Res; 1991 Apr 01; 51(7):1803-10. PubMed ID: 2004365 [Abstract] [Full Text] [Related]
5. Phase I trial using adaptive control dosing of hexamethylene bisacetamide (NSC 95580). Conley BA, Forrest A, Egorin MJ, Zuhowski EG, Sinibaldi V, Van Echo DA. Cancer Res; 1989 Jun 15; 49(12):3436-40. PubMed ID: 2720696 [Abstract] [Full Text] [Related]
6. A phase I and pharmacological study of protracted infusions of crisnatol mesylate in patients with solid malignancies. Villalona-Calero MA, Petit T, Kuhn J, Cobb P, Kraynak M, Eckhardt SG, Drengler R, Simmons C, Santabarbara P, Von Hoff DD, Rowinsky EK. Clin Cancer Res; 1999 Nov 15; 5(11):3369-78. PubMed ID: 10589747 [Abstract] [Full Text] [Related]
7. Phase I clinical trial and pharmacokinetic study of the spicamycin analog KRN5500 administered as a 1-hour intravenous infusion for five consecutive days to patients with refractory solid tumors. Supko JG, Eder JP, Ryan DP, Seiden MV, Lynch TJ, Amrein PC, Kufe DW, Clark JW. Clin Cancer Res; 2003 Nov 01; 9(14):5178-86. PubMed ID: 14613997 [Abstract] [Full Text] [Related]
8. A dose-seeking trial of edatrexate in combination with vinblastine, adriamycin, cisplatin, and filgrastim (EVAC/G-CSF) in patients with advanced malignancies: promising antineoplastic activity against non-small cell lung carcinomas. Colón-Otero G, Marschke R, Camoriano JK, Sorensen JM, Sloan JA, Richardson RL. Cancer J Sci Am; 1997 Nov 01; 3(5):297-302. PubMed ID: 9327154 [Abstract] [Full Text] [Related]
18. Phase I trial of intraperitoneal iododeoxyuridine with and without intravenous high-dose folinic acid in the treatment of advanced malignancies primarily confined to the peritoneal cavity: flow cytometric and pharmacokinetic analysis. Morgan RJ, Newman EM, Doroshow JH, McGonigle K, Margolin K, Raschko J, Chow W, Somlo G, Leong L, Tetef M, Shibata S, Hamasaki V, Carroll M, Vasilev S, Akman S, Coluzzi P, Wagman L, Longmate J, Paz B, Yen Y, Klevecz R. Cancer Res; 1998 Jul 01; 58(13):2793-800. PubMed ID: 9661893 [Abstract] [Full Text] [Related]
19. Phase I and pharmacokinetic study of triapine, a potent ribonucleotide reductase inhibitor, administered daily for five days in patients with advanced solid tumors. Murren J, Modiano M, Clairmont C, Lambert P, Savaraj N, Doyle T, Sznol M. Clin Cancer Res; 2003 Sep 15; 9(11):4092-100. PubMed ID: 14519631 [Abstract] [Full Text] [Related]