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  • Appetite suppressants and heart valve disorders
  • Supraadditive effect of d-fenfluramine plus phentermine on extracellular acetylcholine in the nucleus accumbens: possible mechanism for inhibition of excessive feeding and drug abuse.
  • Effects of phentermine and fenfluramine on extracellular dopamine and serotonin in rat nucleus accumbens: therapeutic implications.
  • Characterization of phentermine and related compounds as monoamine oxidase (MAO) inhibitors.
  • Diet drug-related cardiac valve disease: the Mayo Clinic echocardiographic laboratory experience.
  • Fluoxetine increases the anorectic and long-term dopamine-depleting effects of phentermine.
  • High performance liquid chromatography with UV detection for the simultaneous determination of sympathomimetic amines using 4-(4,5-diphenyl-1H-imidazole-2-yl)benzoyl chloride as a label.
  • Additive effects on rat brain 5HT release of combining phentermine with dexfenfluramine.
  • Fluorometric determination of DL-fenfluramine, DL-norfenfluramine and phentermine in plasma by achiral and chiral high-performance liquid chromatography.
  • Phentermine inhibition of recombinant human liver monoamine oxidases A and B.
  • Properties of microsomal enzyme systems that reduce N-hydroxyphentermine.
  • The effect of propranolol phentolamine and pimozide on drug-induced anorexia in the mouse.
  • Quantitative analysis of human heart valves: does anorexigen exposure produce a distinctive morphological lesion?
  • Intestinal metabolism of mephentermine and its biliary metabolites in male Wistar rats.
  • The formation of metabolites of mephentermine by microsomal and cytosolic preparations of male Wistar rat livers.
  • Standardization of a multi-wavelength UV detector for liquid chromatography-based toxicological analysis.
  • Influence of a pre-existing phospholipidosis on the accumulation of amiodarone and desethylamiodarone in rat alveolar macrophages.
  • Anterior polar cataract and lysosomal alterations in the lens of rats treated with the amphiphilic lipidosis-inducing drugs chloroquine and chlorphentermine.
  • Isolation of urinary p-hydroxylated metabolites of mephentermine and phentermine in male Wistar rats.
  • The disposition of phentermine and its N-oxidized metabolic products in the rabbit.
  • Newborn response to cationic amphiphilic drugs.
  • Lipidosislike renal changes in rats treated with chlorphentermine or with tricyclic antidepressants.
  • Effects of drug-induced pulmonary phospholipidosis on lung mechanics in rats.
  • Prevention of chlorphentermine-induced pulmonary phospholipidosis in rats by phenobarbital.
  • Complications in the cardiovascular system from neuroleptic treatment
  • Mechanism of oxidation of N-hydroxyphentermine by superoxide.
  • Association of chlorphentermine with phospholipids in rat alveolar lavage materials, alveolar macrophages and type II cells.
  • Chlorphentermine may produce dual stimulus effects: a preliminary investigation.
  • N-11C-Methylchlorphentermine and N,N-11C-dimethylchlorphentermine as brain blood-flow agents for positron emission tomography.
  • Action of fenfluramine, phenylpropanolamine, phentermine and diethylpropion on acoustic startle in rats.
  • Effect of chlorphentermine on incorporation of 14Ccholine in the rat lung phospholipids.
  • Mitochondrial alterations in the brain of the rat caused by chlorphentermine.
  • Alterations in peripheral nerves of rats treated with chlorphentermine or with iprindole.
  • Are the renin-containing granules of juxtaglomerular epithelioid cells modified lysosomes?
  • Role of the alveolar macrophage in the induction of pulmonary phospholipidosis by chlorphentermine. II. Drug uptake into cells in vitro.
  • Chlorphentermine-induced biochemical alterations in mitochondrial membranes.
  • Preparation and evaluation of 3-125Iiodo-4-aminophentermine as a brain perfusion imaging agent. Comparison with labeled phentermine derivatives.
  • Morphological and biochemical alterations of the lung after application of chlorphentermine.
  • Generalized lipidosis in newborn rats and Guinea pigs induced during prenatal development by administration of amphiphilic drugs to pregnant animals.
  • Chlorphentermine-induced changes of the peripheral vestibular sense organ of the rat.
  • Multinucleation in alveolar macrophages from rats treated with chlorphentermine.
  • Ion exchange method for determining mephentermine sulfate in drug formulations: collaborative study.
  • Chlorphentermine-induced lipidosis of the cochlea and the cochlear nucleus
  • Effect of chlorphentermine on the lipids of rat lungs.
  • Alterations in monoamine oxidase activity after single and repeated exposure of rats to chlorphentermine.
  • Chlorphentermine-induced alterations in pulmonary phospholipid content in rats.
  • Corneal lipidosis in rats treated with amphiphilic cationic drugs.
  • Phospholipidosis in the alveolar macrophage induced by cationic amphiphilic drugs.
  • Particle binding, phagocytosis, and plastic substrate adherence characteristics of alveolar macrophages from rats acutely treated with chlorphentermine.
  • Chlorphentermine-induced alterations in the lungs of vitamin E-deficient and supplemented rats: 1. Biochemical and morphometric analysis of the pulmonary response.
  • Negative-ion mass spectrometry of amphetamine congeners.
  • Neonatal toxicity in rats following in utero exposure to chlorphentermine or phentermine.
  • Impairment of renal function in rats with generalized lipidosis as induced by chlorphentermine.
  • A compartmental model for the uptake of chlorphentermine in isolated perfused rat lung.
  • Drug-induced phospholipidosis. II. Alterations in the phospholipid pattern of organs from mice, rats and guinea-pigs after chronic treatment with chlorphentermine.
  • Modification by phenobarbital of chlorphentermine-induced changes in lung morphology and drug-metabolizing enzymes in newborn rats.
  • Effects of several lipidosis-including drugs upon the area postrema and adjacent medullary nuclei of adult rats. I. Alterations is perikarya and dendrites.
  • In vivo and in vitro reversibility of chlorphentermine-induced phospholipidosis in rat alveolar macrophages.
  • Chlorphentermine-induced lipidosis in the rat retina: a functional and morphological study.
  • Experimentally induced lipidosis in uterine and vaginal epithelium of rats.
  • Metabolism of mephentermine and its derivatives by the microsomal fraction from male Wistar rat livers.
  • Influence of some sympathomimetic amines on the experimental gastric ulcers in rats.
  • Phentermine+fenfluramine produce cocaine-like discriminative cues.
  • Combined phentermine/fenfluramine administration enhances depletion of serotonin from central terminal fields.
  • Cardiac valvulopathy associated with exposure to fenfluramine or dexfenfluramine: U.S. Department of Health and Human Services interim public health recommendations, November 1997.
  • Chloroquine- and chlorphentermin-induced lipidosis in rat retina
  • Effects of phentermine on striatal dopamine and serotonin release in conscious rats: in vivo microdialysis study.
  • Efficacy of administration of dexfenfluramine and phentermine, alone and in combination, on ingestive behavior and body weight in rats.
  • The fen-phen finale: a study of weight loss and valvular heart disease.
  • The prevalence of cardiac valvular insufficiency assessed by transthoracic echocardiography in obese patients treated with appetite-suppressant drugs.
  • Effects of fenfluramine and phentermine (fen-phen) on dopamine and serotonin release in rat striatum: in vivo microdialysis study in conscious animals.
  • Metabolic N-oxidation products of aliphatic amines as potential mediators in amine pharmacology.
  • Clinical-pharmacological studies on the effect of mephentermin and methamphetamine on the hemodynamics of the lung circulation
  • The effect of seven vasopressors of halothane MAC in dogs.
  • Metabolic and inotropic effects of verapamil in perfused rat heart.
  • The identification and analysis of the metabolic products of mephentermine.
  • Ionamin online references
  • Beneficial effects of pharmacotherapy on weight loss, depressive symptoms, and eating patterns in obese binge eaters and non-binge eaters.







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