Pyridoxine and anergy in Hodgkin's disease.
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Hodgkin Disease↗
Biomedical subjects
V T Oliverio
Publications and source records attributed to V T Oliverio.
Abnormalities of tryptophan metabolism and plasma pyridoxal phosphate in Hodgkin's disease.
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Adolescent↗
Reinvestigation of methotrexate metabolism in rodents.
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Animals↗
Preliminary pharmacologic and clinical evaluation of camptothecin sodium (NSC-100880).
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Adenocarcinoma↗
The absorption, distribution, excretion, and biotransformation of the carcinostatic 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea in animals.
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Animals↗
The uptake, distribution, and antitumor activity of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea in the murine glioma.
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Animals↗
Antibiotics alter methotrexate metabolism and excretion.
The chemotherapeutic agent methotrexate is metabolized by the intestinal flora of normal mice. This metabolism is reduced either by treatment of mice with the antibiotics neomycin and sulfathiazole, or in germ-free mice. In addition to affecting metabolism, these antibiotics alter physiological distribution of methotrexate so that excretion by the intestinal route is significantly enhanced.
Animals↗
Characteristics of folic acid transport in the L1210 leukemia cell.
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Animals↗
Plasma pyridoxal phosphate depletion by the carcinostatic procarbazine.
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Animals↗
A fluorometric method for determination of camptothecin in plasma and urine.
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Alkaloids↗
Comparative carcinogenicity of N-isopropyl-alpha-(2-methylhydraziono)-p-toluamide. HCI (procarbazine hydrochloride), its degradation products, other hydrazines, and isonicotinic acid hydrazide.
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Amides↗
Carrier-mediated transport of the folic acid analogue, methotrexate, in the L1210 leukemia cell.
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Animals↗
Antitumor activity and some pharmacologic properties of anthramycin methyl ether.
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Animals↗
Studies of resistance to methylglyoxal-bis-guanylhydrazone and its metabolic fate in tumor-bearing rodents.
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Animals↗
Monoamine oxidase inhibition by a new carcinostatic agent, N-isopropyl-a92-methylhydrazino)-p-toluamide (MIH).
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Animals↗
The metabolic fate of tritiated methotrexate. II. Absorption and excretion in man.
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Adult↗
The metabolic fate of tritiated methotrexate. I. Absorption, excretion, and distribution in mice, rats, dogs and monkeys.
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Animals↗
The physiological disposition of the carcinostatic 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) in man and animals.
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Animals↗