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Bocksberger JP, Gachoud JP, Richard J, Dick P. Comparison of the efficacy of moclobemide and fluvoxamine in elderly patients with a severe depressive episode. Eur Psychiatry 1993; 8: 319324. Bougerol T, Uchida C, Gachoud JP, Kohler M, Mikkelsen H. Efficacy and tolerability of moclobemide compared with fluvoxamine in depressive disorder DSM III ; . A French Swiss double-blind trial. Psychopharmacology 1992; 106 Suppl ; : S102108. Bramanti P, Ricci RM, Roncari R et al. An Italian multicenter experience with fluvoxamine, a new antidepressant drug, versus imipramine. Curr Ther Res Clin Exp 1988; 43: 718725. de Jonghe F, Swinkels J, Tuynman-Qua H. Randomized doubleblind study of fluvoxamine and maprotiline in treatment of depression. Pharmacopsychiatry 1991b; 24: 2127. De Wilde JE, Mertens C, Walekin JS. Clinical trials of fluvoxamine vs chlorimipramine with single and three times daily dosing. Br J Clin Pharmacol 1983; 15: 427431. Dick P, Ferro E. A double-blind comparative study of the clinical efficacy of fluvoxamine and chlorimipramine. Br J Clin Pharmacol 1983; 15: 419s425s. Dominguez RA, Goldstein BJ, Jacobsen AF, Steinbook RM. A double-blind controlled study of fluvoxamine and imipramine in depression. J Clin Psychiatr 1985; 46: 8487. Gonella G, Baignoli G, Ecari U. Fluvoxamine and imipramine in the treatment of depressive patients: a double-blind controlled study. Curr Med Res Opin 1990; 12: 177184. Guelfi JD, Dreyfus JF, Pichot P, GEPECP. A double-blind placebo controlled clinical trial comparing fluvoxamine with imipramine. Br J Clin Pharmacol 1983; 15: 411s417s. Harris B, Szulecka TK, Anstee JA. Fluvoxamine versus amitriptyline in depressed hospital out patients: a multicentre doubleblind comparative trial. Br J Clin Res 1991; 2: 8999. Itil TM, Shrivastava RK, Mukherjee S, Coleman BS, Michael ST. A double-blind placebo-controlled study of fluvoxamine and imipramine in out patients with primary depression. Br J Clin Pharmacol 1983; 15: 433s438s Kasper S, Voll G, Vieira A, Kick H. Response to total sleep deprivation before and during treatment with fluvoxamine or maprotiline in patients with major depression--results of a double-blind study. Pharmacopsychiatry 1990; 23: 135142. Klok CJ, Brouwer GJ, Van Praag HM, Doogan D. Flovoxamine and clomipramine in depressed patients: a double-blind clinical study. Acta Psychiatr Scand 1981; 64: 111. Lapierre YD, Browne M, Horn E et al. Treatment of major affective disorder with fluvoxamine. J Clin Psychiatr 1987; 48: 6568. Lydiard RB, Laird LK, Morton WA Jr et al. Fluvoxamine, imipramine, and placebo in the treatment of depressed outpatients: effects on depression. Psychopharmacol Bull 1989; 25: 6870. March JS, Kobak KA, Jefferson JW, Mazza J, Greist JH. A doubleblind, placebo-controlled trial of fluvoxamine versus imipramine in outpatients with major depression. J Clin Psychiatr 1990; 51: 200202. Mullin JM, Pandita-Gunawardena VR, Whitehead AM. A doubleblind comparison of fluvoxamine and dothiepin in the treatment of major affective disorder. Br J Clin Pract 1988; 42: 5155. Nathan RS, Perel JM, Pollack BG, Kupfer DJ. The role of neuropharmacologic selectivity in antidepressant action: fluvoxamine versus desipramine. J Clin Psychiatr 1990; 51: 367372. Norton KRW, Sireling LI, Bhat AV, Rao B, Paykel ES. A doubleblind comparison of fluvoxamine, imipramine and placebo in depressed patients. J Affect Disord 1984; 7: 297308. Ottevanger EA. Fluvoxamine and clomipramine in depressed hospitalised patients: results from a randomised, double-blind study. Encephale 1995; 21: 317321. Perez A, Ashford JJ. A double-blind, randomized comparison of fluvoxamine with mianserin in depressive illness. Curr Med Res Opin 1990; 12: 234241. Phanjoo AL, Wonnacott S, Hodgson A. Double-blind comparative multicentre study of fluvoxamine and mianserin in the treatment of major depressive episode in elderly people. Acta Psychiatr Scand 1991; 83: 476479.

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Includes family members in treatment as well as clients dealing with their own alcohol, drug and or gambling problem. 2 The total of open individuals and new individuals does not sum across the rows due to the statistical procedure for removing duplicate cases. That is, duplicate counts are deletedwithin each service category to yield open or new cases within that category only. Under the provincial total, all duplicates are deleted across the service categories. Of a total of 2098 patients with ARF seen between January 1990 and December 1999, 124 had renal failure due to malaria. Plasmodium falciparum was responsible for 121. The remaining three had P.vivax on peripheral blood smears. There were 99 males and 25 females with a mean age of 33.5 17.2 years range: 575 years ; . Their presenting clinical features are shown in Table 1. All were febrile and a majority had oligo- or anuria; jaundice was detected in 62 50% ; patients on presentation. CNS involvement of varying severity, ranging from depressed sensorium to frank coma, was present in 50 patients. Laboratory parameters are shown in Tables 2 and 3. Moderate reduction in haemoglobin was common. Thrombocytopenia, a platelet count 150 000 mm3, was present in 87 patients. Serum LDH was tested in 39 patients and in 31 it was 500 IU l. The hyperbilirubinaemia of almost all icteric patients was of the conjugated variety.
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Wellman 84 the river. He said the new museum might be built in two or three years and that it would cost about 5 million dollars. We began talking about the real purpose of the museum. He said, "To provide a social place, to start the Green Corn Ceremony22 again." James told me the story of Gluskap, the first man and the first woman. He told me that the first woman gave her body so that the people had resources. Her bones became corn. The new museum, he explained, could revive this ceremony. He told me how he'd grown up with it every year when he was a kid, but for the past 30 years they didn't do it. I asked why, and he said it was because of volunteerism. The same people had been doing it year after year. He spoke so fervently that my eyes became glossy with the strength of his dream. He spoke of pride in "Penobscot identity" and the importance of having a place for ceremonies and dance. James' desire to have a new museum on the island and a field for dancing is linked to his strong connection to the island and his memories of the Green Corn Ceremony. According to James, the Green Corn Ceremony occurred once a year at the time of the first harvest. It was a festival in which people celebrated Penobscot identity and continued traditions. James' foremost concern is for his people and their needs. One day, he told me about cultural day at his son's school and how they had invited male Penobscot to dance. "The boys were too shy. They didn't want to dance. There was a bad feeling, " James said. "What we need are male role models who weren't afraid to get up there and dance." He looked me in the eye as he spoke. This time, however, James said that he had gone to his son's cultural day and that there were other Indians there. Some were dressed up with normal work cloths and others in traditional garments. "I wore my rainbow suit, " he told me. He leaned back on one of the basket cases, "They all danced and my son joined. People in the audience joined. I want. Study 083 Study 084 A double-blind comparative study of the effects of paroxetine and clomipramine on cognitive function in elderly patients with major depression A controlled double-blind randomised parallel group study comparing the effects of paroxetine and maprotiline in the treatment of outpatients with major and minor depression [RDC] DFG 29060 III 86 1 23 DFG 29060 III 86 1 24M A randomised, double-blind comparative study of paroxetine and imipramine including evaluation of effect profiles and correlation between plasma concentration and effect. A randomised double-blind comparative clinical study of paroxetine and imipramine including evaluation of efficacy profiles and safety A double-blind controlled group comparison of paroxetine and imipramine in the treatment of depressive states in psychiatric specialist practice A double-blind comparative study to assess the safety and tolerability of paroxetine 60mg two dosing regimins ; . Short and long-term. A double-blind comparative study of the withdrawal effects following abrupt discontinuation of treatment with paroxetine and mazindol.

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Corresponding author. Department of Microbiology--Infectious Disease, Hopital Maisonneuve-Rosemont, 5415 boul de l'Assomption, Montreal, Quebec, Canada H1T 2M4. Tel: + 1-514-252-3817; Fax: + 1-514-252-3898; E-mail: laverdim courrier.umontreal!

Historically, it has been standard practice to use a linear time-integrated concentration i.e., C T, CT, or dosage ; to predict mortality-response relationships for chemical vapor exposures. The above concept has persisted as an accepted principle in military hazard assessment, currently serving as the basis for estimating injury from exposure to chemical and mecamylamine. The introduction of the 3 bin kerbside collection system has been a huge success for the collection of residential recycling and waste material. The City of Greater Geelong has adopted Best Practice and is seen as a leader in this area. Other initiatives introduced by the Council include: 1 ; The use of recycled paper within the organisation; 2 ; Water sensitive urban designs; 3 ; Efficient watering management of Council's assets; 4 ; Use of recycling bins within Council buildings; 5 ; Using recycled materials for construction purposes; 6 ; "Eco-Buy" - purchasing group for buying products made from recycled materials; 7 ; "Butt bins" at most offices; and 8 ; Lighting systems movement and brightness sensitive to reduce power consumption. Council needs to operate under the Waste Wise flag to give weight to its claim of leading in best practice waste management. Council has identified in its Waste Education Strategy that encouraging Waste Wise Schools, Community Groups and event managers is a key to reaching targets set, and adopted by Council, of EcoRecycling Victoria's Towards Zero Waste strategy.

Recent clinical studies where administration of an antiresorptive bisphosphonate in combination with PTH did not augment the increase in bone volume. Bisphosphonates have been shown to inhibit osteoclast activity at four levels: 1 ; inhibition of osteoclast recruitment, 2 ; inhibition of osteoclast adhesion, 3 ; shortening of osteoclast lifespan, and 4 ; direct inhibition of osteoclast activity 47 ; . According to the hypothesis presented here, the alteration in recruitment would impact the anabolic action of PTH, but the other actions should not compromise cells that may be key targets for anabolic actions of PTH. Furthermore, studies of combinatorial therapy where the antiresorptive calcitonin was administered in combination with PTH did not prove to augment the anabolic action of PTH 48 ; . In contrast, one study reported that the combination of OPG with PTH did not compromise the increase in bone strength that PTH mediated 49 however, this study was performed in rats and under an estrogen-depleted condition that could have modified the outcome. Other reports highlight cross talk mechanisms between osteoclasts and osteoblasts 50, 51 ; . Two preliminary studies suggest a juxtacrine interaction between osteoclasts and osteoblasts 52, 53 ; . To our knowledge, the present study is the first to provide data to support the role of osteoclastic cells in the action of an anabolic agent although it has been proposed 54 ; . Recent data support the concept of a stage-dependent impact of osteoclasts on the bone formation response. Pharmaceutical strategies were used to inhibit osteoclast acidification, and the data indicated that resorption could be inhibited at this late stage of osteoclast differentiation without altering bone formation 55 ; . Hence, the data presented here and in conjunction with other studies strongly suggest that cells in the intermediately differentiated population of osteoclasts may be key targets for PTH anabolic action. Interestingly, that cells in the marrow were targets of PTH action was proposed more than 10 years ago, but perhaps because of the focus then on catabolic actions of PTH, little was done to substantiate this work in regards to anabolic actions 56 ; . It also important to recognize that although the model system used here is not a model of osteoporosis but may be more applicable to clinical scenarios in bone regeneration for local tissue engineering strategies where PTH has also been found to be anabolic 57, 58 ; . Previous work from our laboratory and others indicate that cells of the osteoblastic lineage are critical for anabolic actions, but our in vitro data suggest that they are not the direct targets of PTH action for this anabolic effect. This does not preclude their ability to, while directly inhibiting mineralization, produce factor s ; that signal to cells in the marrow that then direct other osteoblastic cells to form bone. This multilevel regulation may also address the vagaries of an intermittent PTH administration regimen. Data from our ossicle model system point to a role of cells of the osteoblast lineage that are relatively early in their differentiation program and are not lining or terminally differentiated cells 28 ; . Collectively, these current and recent studies suggest that PTH targets stromal cells to signal to cells of the hematopoietic lineage to recruit to sites of remodeling. These cells differentiate and multinucleate, and before adhering to the bone matrix and resorbing bone, they signal either via a and mechlorethamine.

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Introduction List of icons 1. 2. 3. amitriptyline amoxapine atomoxetine bupropion citalopram clomipramine desipramine dothiepin doxepin duloxetine escitalopram fluoxetine fluvoxamine imipramine isocarboxazid lofepramine maprotiline milnacipran mirtazapine moclobemide nefazodone nortriptyline paroxetine phenelzine protriptyline reboxetine selegiline sertraline tianeptine tranylcypromine trazodone trimipramine venlafaxine ix xi 1. ANTIRETROVIRALS NRTIs- abacavir Ziagen ; , abacavir lamivudine zidovudine Trizivir ; , didanosine ddI, Videx ; , lamivudine Epivir, 3TC ; , lamivudine zidovudine Combivir ; , stavudine d4T, Zerit ; , tenofovir Viread ; , zalcitabine ddC, HIVID ; , zidovudine AZT, Retrovir ; . PIs- amprenavir Agenerase ; , indinavir Crixivan ; , lopinavir ritonavir Kaletra ; , nelfinavir Viracept ; , ritonavir Norvir ; , saquinavir Fortovase, Invirase ; . NnRTIs- delavirdine Rescriptor ; , efavirenz Sustiva ; , nevirapine Viramune ; . Other- hydroxyurea Hydrea ; . OI DRUGS PHS "A1 OI"s- acyclovir Zovirax ; , azithromycin Zithromax ; , cidofovir Vistide ; , clarithromycin Biaxin ; , famciclovir Famvir ; , fluconazole Diflucan ; , foscarnet Foscavir ; , ganciclovir Cytovene ; , isoniazid Nydrazid, Rifamate, Rifater ; , itraconazole Sporonox ; , leucovorin, pyrazinamide Rifater ; , pyrimethamine Daraprim, Fansidar ; , rifampim Rifamate, Rifater, Rifadin, Rimactane ; , sulfadiazine, TMP SMX Bactrim, Cotrim, Septra ; . Other OIs- amikacin, atovaquone Mepron ; , ciprofloxacin Cipro ; , clindamycin Cleocin, Clinda-Derm ; , clotrimazole Mycelex ; , cycloserine Seromycin ; , dapsone, daunorubicin DaunoXome ; , doxorubicin Adriamycin, DOXIL, Rubex ; , epoetin alfa Epogen, Procrit ; , ethambutol Myambutol ; , ethionamide Trecator ; , fomivirsen sodium IV Vitravene ; , filgrastim Neupogen ; , ketoconazole Nizoral ; , metronidazole Flagyl ; , ofloxacin Floxin ; , para aminosalicyclic acid PAS ; , pentamidine Nebupent ; , rifabutin Mycobutin ; , streptomycin, trimetrexate glucuronate Neutrexin ; , valacyclovir Valtrex ; . Hepatitis C- Interferon alfa 2a, 2b Intron A, RoferonA ; . TREATMENTS FOR METABOLIC DISORDERS Diabetic- acarbose Precose ; , chlorpropamide Diabinese ; , metformin HCI Glucophage ; , glimepride Amaryl ; , glipizide Glucotrol ; , glyburide DiaBeta, Glynase, Micronase ; , insulins all insulins ; . Hyperlipidemia- atorvastatin lipitor ; , clofribate Atromid ; , gemfibrozil Lopid ; , fluvastatin Lescol ; , lovastatin Mevacor ; , pravastatin Pravachol ; , simvastatin Zocor ; . Wasting- dronabinol Marinol ; , megestrol acetate Megace ; , nandrolone decanoate Deca-Durabolin ; , oxandrolone Oxandrin ; , testosterone cypionate Birilon IM ; , testerone enanthate Delatestryl ; , thalidomide. ALL OTHERS acetaminophen various ; , alfentanil Alfenta ; , alglucerase Ceredase ; , alteplase Activase ; , amitriptyline Elavil, Etrafon, Triavil, Limbitrol ; , amoxapine Asendin ; , amoxicillin Amoxil, Wymox ; , amoxicillin calvulanate potassium Augmentin ; , ampicillin sodium sulbactam sodium Unasyn ; , Arco-Lase Plus, asparaginase Elspar ; , aspirin Easprin ; , buprenorphine Buprenex ; , buproprion Wellbutrin ; , buspirone Buspar ; , butalbital Various ; , carbamezapine Atretol, Tegretol, Epitol ; , cefazolin sodium Ancef, Kefzol ; , chlordiazepoxide Limbitrol ; , choline Trilisate ; , clonazepam Klonopin ; , clorazepate Tranxene, Gen-xene ; , codine Various ; , desipramine Norpramin ; , dezocine Dalgan ; , diazepam Dizac, Balium ; , diclofenac Cataflam, Voltaren ; , difenoxin HCI Motofen ; , diflunisal Dolobid ; , dihydrocodeine DHCplus, Synalgos ; , diphenoxylate HCI Lomotil ; , disoium clavulanate potassium Timentin ; , doxepin Adapin, Sinequan, Zonalon ; , doxycycline calcium Vibramycin Calcium ; , enoxacin Penetrex ; , erythromycin all forms ; , ethosuximide Zarontin ; , ethotoin Peganone ; , etodolac Lodine ; , felbamate Felbatol ; , fenoprofen Nalfon ; , fentanyl Duragesic, Sublimaze ; , fluoxetine Prozac ; , fosphenytoin Cerebyx ; , furazolidone Furoxone ; , gabapentin Neurontin ; , gentamicin Garamycin, G-myticin ; , hepatitis A vaccine, hepatitis B vaccine, h. influenza B vaccine, hydrocodone Various ; , hydromorphone Dilaudid ; , ibuprofen IBU, Motrin ; , imiglucerase Cerezyme ; , imipramine Tofranil ; , indomethacin Indocin ; , influenza vaccine, ketoprofen Orudis, Oruvail ; , ketorolac Toradol ; , lamotrigine Lamictal ; , levofloxacin Levaquin ; , levomethadyl Orlaam ; , levorphanol LevoDromoran ; , lomefloxacin HCI Maxaquin ; , loperamide HCI Imodium ; , maprotiline Ludiomil ; , meclizine Antivert ; , mefenamic Ponstel ; , meperidine Demerol, Mepergan ; , mephenytoin Mesantoin ; , mephobarbital Mebaral ; , methadone Dolophine ; , methotrimeprazine Levoprome ; , methasuximide Celontin ; , midrin, mirtazipine Remeron ; , MMR measles, mumps, rubella ; , morphine various ; , nabumetone Relafen ; , nalbuphine Nubain ; , naproxen Anaprox, Naprelan ; , nefazodone Serzone ; , nortriptyline Pamelor ; , octreotide acetate Sandostatin ; , ondansetron HCI Zofran ; , opium Tincture ; , orphenadrine Norflex, Norgesic, Mio-Rel ; , oxaprozin Daypro ; , oxycodone Various ; , oxymorphone Numorphan ; , paroxetine Paxil ; , penicillin Pen-Vee K ; , pegademase Adagen ; , pegaspargase Oncaspar ; , pentazocine Talacen, Talwin ; , pentobarbital Nembutal ; , perphenazine Etrafon, Triavil ; , phenacemide Phenurone ; , phenelzine Nardil ; , phenobarbital, phenytoin Dilantin ; , primidone Mysoline ; , piroxicam Feldene ; , pneumococcal Pneumovax ; , polio vaccine, prochlorperazine Compazine ; , promethazine HCI Phenergan ; , propoxyphene Darvocet, Darvon, Wygesic ; , protriptyline Vivactil ; , salsalate Disalcid, Mono-Gesic, Salflex ; , sertraline Zoloft ; , sufentanil Sufenta ; , sulindac Clinoril ; , tetanus-diptheria vaccine, ticarcillin, tolmetin Tolectin ; , tramadol Ultram ; , tranylcypromine Parnate ; , traumeel, trazodone Desyrel ; , trimethobenzamide HCI Tigan ; , trimipramine Surmontil ; , trovofloxacin Trovicin ; , valproic acid Depakene ; , varicella vaccine, venlaxafine Effexor and meclizine.

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The study was approved by the medical ethics committee of our institution. Informed consent was obtained from all patients. We studied 35 patients Group D ; ranging in age from 35 to 60 who were diagnosed as having major depression according to Diagnostic and Statistical Manual of Mental Disorders, 4th edition, criteria 11 ; and 35 patients Group C ; ranging in age from 35 to 60 who were selected randomly as controls. All depressed patients had been taking antidepressants imipramine, clomipramine, maprotiline, or mianserin ; for more than a year. Clomipramine is a low anticholinergic antagonist, imipramine is a moderate anticholinergic antagonist, and maprotiline and mianserin are low muscarine antagonists. The mean half-life is 21 h for clomipramine, 15 h for imipramine, 46 h for maprotiline, and 18 h for To hydroxyzine, 25-50 mg p.o. t.i.d. He gradually less restless and his abdominal distress abated. We hydroxyzine treatment 14 days after the discontin and medrol. 27. Steiner M, Steinberg S, Stewart D, Carter D, Berger C, Reid R, et al. Fluoxetine in the treatment of premenstrual dysphoria. N Engl J Med 1995; 332: 1529-34. Diegoli MS, da Fonseca AM, Diegoli CA, Pinotti JA. A double-blind trial of four medications to treat severe premenstrual syndrome. Int J Gynaecol Obstet 1998; 62: 63-7. Romano S, Judge R, Dillon J, Shuler C, Sundell K. The role of fluoxetine in the treatment of premenstrual dysphoric disorder. Clin Ther 1999; 21: 615-33. Eriksson E, Hedberg MA, Andersch B, Sunblad C. The serotonin reuptake inhibitor paroxetine is superior to the noradrenaline reuptake inhibitor maprotiline in the treatment of premenstrual syndrome. Neuropsychopharmacology 1995; 12: 167-76. Freeman EW, Rickels K, Sondheimer SJ, Polansky M. Differential response to antidepressants in women with premenstrual syndrome premenstrual dysphoric disorder. Arch Gen Psychiatry 1999; 56: 932-9. Yonkers KA, Halbreich U, Freeman E, Brown C, Endicott J, Frank E, et al. Symptomatic improvement of premenstrual dysphoric disorder with sertraline treatment. JAMA 1997; 278: 983-8. Cohen LS. Sertraline for premenstrual dysphoric disorder. JAMA 1998; 279: 357-8. Sundblad C, Modigh K, Andersch B, Eriksson E. Clomipramine effectively reduces premenstrual irritability and dysphoria. Acta Psychiatr Scand 1992; 85: 39-47. Dimmock PW, Wyatt KM, Jones PW, O'Brien PM. Efficacy of selective serotonin-reuptake inhibitors in premenstrual syndrome. Lancet 2000; 356: 1131-6. Berger CP, Presser B. Alprazolam in the treatment of two subsamples of patients with late luteal phase dysphoric disorder. Obstet Gynecol 1994; 84: 379-85. Freeman EW, Rickels K, Sondheimer SJ, Polansky M. A double-blind trial of oral progesterone, alprazolam, and placebo in treatment of severe premenstrual syndrome. JAMA 1995; 274: 51-7. Hammarbck S, Bckstrom T. Induced anovulation as treatment of premenstrual tension syndrome. Acta Obstet Gynecol Scand 1988; 67: 159-66. Leather AT, Studd JW, Watson NR, Holland EF. The treatment of severe premenstrual syndrome with goserelin with and without `add-back' estrogen therapy. Gynecol Endocrinol 1999; 13: 48-55. Brown CS, Ling FW, Andersen RN, Farmer RG, Arheart KL. Efficacy of depot leuprolide in premenstrual syndrome. Obstet Gynecol 1994; 84: 779-86. Hahn PM, Van Vugt DA, Reid RL. A randomized, placebo-controlled, crossover trial of danazol for the treatment of premenstrual syndrome. Psychoneuroendocrinology 1995; 20: 193-209. Magill PJ. Investigation of the efficacy of progesterone pessaries in the relief of symptoms of premenstrual syndrome. Br J Gen Pract 1995; 45: 589-93. Vanselow W, Dennerstein L, Greenwood KM, de Lignieres B. Effect of progesterone and its 5 alpha and 5 beta metabolites on symptoms of premenstrual syndrome according to route of administration. J Psychosom Obstet Gynaecol 1996; 17: 29-38. Wang M, Hammarbck S, Lindhe BA, Bckstrom T. Treatment of premenstrual syndrome by spironolactone. Acta Obstet Gynecol Scand 1995; 74: 803-8. Meden-Vrtovec H, Vujic D. Bromocriptine Bromergon, Lek ; in the management of premenstrual syndrome. Clin Exp Obstet Gynecol 1992; 19: 242-8 and maprotiline.

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Table 1. Clinical, demographic characteristics, and fasting serum biochemical values of the subjects and mefloquine. 0125 U.S.A. The Use of a New Machining Additive in Ferrous Parts to Improve Machinability Bruce Lindsley, Sunil Patel, Hoeganaes Corporation & Suresh Shah, Gregory Falleur, Chanley Chambers, Cloyes Gear & Products, Inc. 0085 Canada Role of Binder Lubricants in Green Machining Carl Blais, Etienne Robert-Perron, Universit Laval & Sylvain Pelletier, Yannig Thomas, Industrial Materials Institute IMI-CNRC ; 0001 India Studies on the Machining Characteristics of 5%SiC-Aluminum Metal Matrix Composite Krishna Mohana Rao Gurram, P. Chandrasekhar, A. Srinivasa Rao, S. Siva Rama Krishna, N. Muniraja, JNTU College of Engineering.

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