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Deferred income taxes reflect the tax consequences on future years of temporary differences between the tax bases of assets and liabilities and their financial reporting amounts. U.S. income taxes are provided on those earnings of foreign subsidiaries and subsidiaries operating in Puerto Rico under tax incentive grants, which are intended to be remitted to the parent company. Undistributed earnings reinvested indefinitely in foreign subsidiaries as working capital and plant and equipment aggregated , 194, 000 at December 31, 2003. It is not practicable to determine the amount of deferred income taxes not provided on these earnings. Abbott's U.S. income tax returns for 1992 and prior years have been audited by the Internal Revenue Service and are closed. In the U.S., Abbott's income tax returns for years after 1992 are open. Earnings before taxes, and the related provisions for taxes on earnings, were as follows.
Other less common adverse events seen in clinical trials include: 1 case of anaphylactic reaction occurred in Phase 2 following rechallenge of drug after withdrawal due to rash rare urticaria; eosinophilia; transient thrombocytopenia rare and leukopenia 2000 WBC mm3 rare ; . Adverse events during a second year of treatment with leflunomide in clinical trials were consistent with those observed during the first year of treatment and occurred at a similar or lower incidence. In post-marketing experience, the following have been reported rarely: Body as a whole: opportunistic infections, severe infections including sepsis that may be fatal; Gastrointestinal: pancreatitis; Hematologic: agranulocytosis, leukopenia, neutropenia, pancytopenia, thrombocytopenia; Hypersensitivity: angioedema; Hepatic: hepatitis, jaundice cholestasis, severe liver injury such as hepatic failure and acute hepatic necrosis that may be fatal; Respiratory: interstitial lung disease, including interstitial pneumonitis and pulmonary fibrosis, which may be fatal; Nervous system: peripheral neuropathy; Skin and Appendages: erythema multiforme, Stevens-Johnson syndrome, toxic epidermal necrolysis, vasculitis including cutaneous necrotizing vasculitis. Adverse Reactions Pediatric Patients ; The safety of ARAVA was studied in 74 patients with polyarticular course juvenile rheumatoid arthritis ranging in age from 3-17 years 47 patients from the active-controlled study and 27 from an open-label safety and pharmacokinetic study ; . The most common adverse events included abdominal pain, diarrhea, nausea, vomiting, oral ulcers, upper respiratory tract infections, alopecia, rash, headache, and dizziness. Less common adverse events included anemia, hypertension, and weight loss. Fourteen pediatric patients experienced ALT and or AST elevations, nine between 1.2 and 3-fold the upper limit of normal, five between 3 and 8-fold the upper limit of normal. DRUG ABUSE AND DEPENDENCE ARAVA has no known potential for abuse or dependence. OVERDOSAGE In mouse and rat acute toxicology studies, the minimally toxic dose for oral leflunomide was 200 - 500 mg kg and 100 mg kg, respectively approximately 350 times the maximum recommended human dose, respectively ; . There have been reports of chronic overdose in patients taking ARAVA at daily dose up to five times the recommended daily dose and reports of acute overdose in adults or children. There were no adverse events reported in the majority of case reports of overdose. Adverse events were consistent with the safety profile for ARAVA see ADVERSE REACTIONS ; . The most.
Ben-Avraham, Z.: Development of asymmetric basins along continental transform faults, Tectonophysics, 215, 209220, 1992. Ben-Avraham, Z. and Zoback, M.: Transform-normal extension and asymmetric basins: An alternative to pull-apart models, Geology, 20, 423426, 1992. Ben-Avraham, Z. and Tibor, G.: The northern edge of the Gulf of Elat, Tectonophysics, 226, 319 331, Ben-Gai, Y., Freislander, U., and Rotstein, Y.: High resolution seismic survey in Evrona area, Isr. Inst. Pet. Res. Geophys., Rep. 836 121 92, Ben-Gai, Y., Rotstein, Y., and Bartov Y.: High resolution seismic reflection survey in Avrona area, Isr. Inst. Pet. Res. Geophys., Rep. 1 357 93, Bonilla, M. G., Mark, R. K., and Lienkaemper, J. J.: Statistical relations among earthquakes magnitude, surface ruptures length, and surface fault displacement, Bulletin of the Seismol. Soc. of America, 74, 6, 23792411, Enzel, Y., Amit, R., Harrison, J. B. J., and Porat, N.: Morphologic dating of fault scarps and terrace risers in the southern Arava, Israel: Comparison to other age-dating techniques and implications to paleoseismicity, Isr. J. Earth Science, 43, 91103, 1994. Enzel, Y., Amit, R., Porat, N., Zilberman, E., and Harrison, J. B. J.: Estimating the ages of fault scarps in the Arava, Israel, Tectonophysics, 253, 305317, 1996. Freislander, U.: Semi-high resolution seismic reflection survey in Shezaf, Paran and Yotveta areas, Isr. Inst. Pet. Res. Geophys., Rep. 846 257 92, Freislander, U.: The subsurface of the southern Araca Valley Results from Seismic Survey, Isr. Inst. Pet. Res. Geophys., Rep. 846 257 92 c ; , 1995a. Freislander, U.: The subsurface of the central Aravs Valley Results from Seismic Survey, Isr. Inst. Pet. Res. Geophys., Rep. 846 257 92 d ; , 1995b. Freund, R., Garfunkel, Z., Zak, I., Goldberg, M., Weissbrod, T., and Derin, B.: The shear along Dead Sea Rift, Philos. Trans. R. Soc. London A., 267, 107130, 1970. Galli, P.: Active tectonics along the Wadi-Arava Jordan Valley transform fault, J. Geophys. Res., 104, B2, 27772796, 1999. Garfunkel, Z.: Generalized geological map of the Adjacent of the Southern Araca Valley, sheet 2 in Hebrew ; , 1969. Garfunkel, Z.: The Tectonics of the western margins of the southern Arava, Ph.D. thesis, Hebrew Univ., Jerusalem in Hebrew with English abstract ; , 1970. Garfunkel, Z.: Internal structure of the leaky transform rift ; in relation to the plate kinematics, in: Freund, R. and Garfunkel, Z. Eds. ; : Dead Sea Rift, Tectonophysics, 80, 81108, 1981. Garfunkel, Z., Zak, I., and Freund, R.: Active faulting along the Dead Sea transform rift ; , Tectonophysics, 80, 126, 1981. Gerson, R. and Grossman, S.: Later stages in morphotectonic evolution of southern Arwva Valley rift, The State of Israel, Ministry of Energy and Infrastructure, Rep. ES-191, 1991. Gerson, R., Grossman, S., Amit, R., and Greenbaum, N.: Indicators of faulting events and periods of quiescence in desert alluvial fans, Earth Surface Processes and Landforms, 18, 181202, 1993. Gev, I.: Water level at water wells Elat-109 and Elat-106, Evrona, Southern Araava Valley, personal communication, 1999. Joffe, S. and Garfunkel, Z.: Plate kinematics of the circum Red Sea a reevaluation, Tectonophysics, 141, 522, 1987.
To what you have just said. DR. WOOD: Okay. Dr. Farrar?.
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In the course of its returns review, the company determined that in some instances its estimates of inventory in the distribution channel did not properly reflect relevant data in its f-7 king pharmaceuticals, inc notes to consolidated financial statements continued ; possession, and that it thereby inadvertently under-accrued for estimated future chargeback amounts.
Reports of serious hepatic reactions associated with the use of Aventis's disease-modifying antirheumatic drug Arava leflunomide ; have prompted European regulators to require increased liver enzyme monitoring. The European Medicines Evaluation Agency stated that although confounding factors were present in many of the liver injury cases, a causal relationship could not be excluded. The revised label says that the liver enzyme ALT must be checked before therapy initiation and at monthly or more-frequent intervals during the first six months of treatment and every eight weeks thereafter. It also advises against treatment with both Arava and methotrexate [Scrip, 21 March 2001]. Aventis is in discussions with the FDA regarding the need, if any, for labeling changes for Arava. U.S. labeling suggests ALT monitoring at baseline and initially at monthly intervals, then, if stable, at intervals determined by the individual clinical situation [The Pink Sheet, 19 March 2001]. Estrogen Replacement Therapy and Ovarian Cancer Mortality Postmenopausal estrogen use is associated with increased risk for endometrial and breast cancer, but an association with ovarian cancer is not established and didronel.
In any situation in which the decision is made to switch from ARAVA to another anti-rheumatic agent with a known potential for haematologic suppression, it would be prudent to monitor for haematologic toxicity, because there will be overlap of systemic exposure to both compounds. ARAVA washout with cholestyramine or charcoal may decrease this risk, but also may induce disease worsening if the patient had been responding to ARAVA treatment. In dogs treated with leflunomide, a delayed healing of accidental cornea lesions was observed. This effect may be attributed to the immunosuppressive effect of leflunomide. Its clinical relevance is, however, unclear. Patients with tuberculin reactivity must be carefully monitored because of the risk of tuberculosis reactivation. Antigenicity ARAVA was not antigenic in the active systemic and passive cutaneous anaphylaxis test in guinea pigs and was devoid of sensitising properties. Mutagenicity Leflunomide A771726 ; was not mutagenic in bacteria Salmonella typhimurium and Escherichia coli ; or Chinese hamster ovary cells, did not cause chromosomal damage in vivo mouse and Chinese hamster bone marrow cells ; , and did not induce unscheduled synthesis of DNA in vitro in mammalian cells. A minor metabolite of leflunomide, trifluoromethylaniline, was mutagenic and caused chromosomal damage in in vitro assays, but it did not cause chromosomal damage in vivo Chinese hamster bone marrow cells ; at concentrations higher than those expected in humans. Carcinogenicity A two year carcinogenicity study of oral leflunomide in mice showed an increased incidence of malignant lymphoma in males given leflunomide 15 mg kg day [associated with plasma A771726 concentrations AUC ; similar to that expected in humans], an increase in bronchioalveolar adenomas in males given 5 mg kg day A771726 AUC similar to or about 50% lower than that expected in humans ; and an increase in bronchioalveolar adenomas and carcinomas in females given 1.5 mg kg day A771726 AUC at least 10-20 times lower than that expected in humans ; . The increase in the development of malignant lymphomas was probably due to the immunosuppressant effect of leflunomide. A no-effect dose or AUC for the development of lung tumours in female mice was not established, but the relevance of these findings for humans was not clear. Leflunomide showed no carcinogenicity activity in rats given oral leflunomide at doses up to 6 mg kg day associated with A771726 AUC 25-65 times lower than that expected in humans ; . The risk of malignancy, particularly lymphoproliferative disorders, is increased with the use of some immunosuppression medications. There is a potential for immunosuppression with ARAVA. No apparent increase in the incidence of malignancies and lymphoproliferative disorders was reported in the clinical trials of ARAVA, but larger and longer-term studies would be needed to determine whether there is an increased risk of malignancy or lymphoproliferative disorders with ARAVA. Effects on Fertility Oral administration of leflunomide at doses up to 4 mg kg day plasma A771726 concentrations AUC ; about 10-25 times lower than that expected in humans] in rats had no effect on fertility, however, impairment of spermatogenesis has been observed in rats, dogs and mice treated with oral leflunomide at higher doses or for longer periods plasma A771726 AUC similar to or much lower than that expected in humans ; . Use in Pregnancy Category X ; As A771726 is teratogenic in rats and rabbits; it may cause foetal harm in humans. ARAVA must not be given to pregnant women, or women of childbearing potential who are not using reliable contraception during treatment with ARAVA and for a certain period of time thereafter waiting period or abbreviated wash-out period; see below ; . Pregnancy must be excluded before the start of treatment with ARAVA. It is recommended that women of childbearing potential only receive ARAVA after it has been confirmed that they are using a reliable form of contraception. In a study in which ARAVA was Arava DS MKT #30095v3.0 Page 12.
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| Arava 2007Biologic response modifiers are genetically engineered drugs that interfere with specific components of the autoimmune response. Because of their precise targets, these drugs do not damage the entire immune system the way that general immunosuppressants do. They are producing dramatic results in some studies. T-Cells-Blockers. Alefacept Amevive ; blocks overactive T-cells, but appears to leave other immune factors alone. It has been approved for moderate to severe plaque psoriasis. Studies report that between 40% to 71% of patients experience at least a 50% improvement in symptoms, and the response appears to persist and even improve in many people. In a few patients the psoriasis worsened. ; Response rates have been better than those observed with methotrexate. Of concern is possible liver toxicity in some patients and a risk for infections. Alefacept may pose less risk for infections than other biologic agents or immunosuppressants, however. Efalizumab Raptiva ; is a particularly promising T-cell blocker that is awaiting approval. In one study, up to 58% of patients achieved a 75% or greater improvement in symptoms. Tumor Necrosis Factor Blockers. Etanercept Enbrel ; and infliximab Remicade ; block tumor necrosis factor TNF ; , an inflammatory immune factor called a cytokine that is very important in the psoriasis disease process. Both TNF-blocking agents are given by injection. Enbrel has been approved for treating psoriatic arthritic and Remicade is awaiting approval. Both agents are proving to be effective for moderate-to-severe psoriasis as well. In a 2003 study of infliximab, by week 10 up to 88% of patient who took the drug experienced improvement that was equal or greater than 75%. Higher rates were observed with higher doses. ; Studies also report that about half of patients taking etanercept show significant improvement. Side effects usually reported in studies of patients taking these agents for rheumatoid arthritis ; include the following: The most common adverse effects of all three are minor reactions at the injection site, but there are few other immediate side effects. Because these agents affect immune factors, there is some risk for severe infections particularly in susceptible individuals, such as those with uncontrolled diabetes, people taking other immunosuppressants, or anyone with a current active infection. For example, cases of tuberculosis and histoplasmosis a fungal infection in the lungs ; have been reported in patients taking TNF-modifiers. While millions of healthy people unknowingly carry the TB organism, it does not become active in most people with healthy immune systems. ; Patients should be tested for TB before initiating treatment. There have been a few reports of aplastic anemia. In rare cases, both etanercept and infliximab have been associated with nerve damage that resembles the disease process in multiple sclerosis. This involves demyelination the loss of myelin, the insulation coat over nerve fibers ; and can result in confusion, numbness, changes in vision, and difficulty walking. There have been reports of a lupus-like symptoms in a few patients taking these drugs, but it is not clear if such findings are significant. To date, the symptoms have resolved when patients stopped taking the drugs. Many patients develop an immune reaction to infliximab itself, which makes the drug less effective overtime. Nevertheless, in one study, benefits persisted for at least two years after stopping the drug. Infliximab has been linked to a few deaths in patients with pre-existing congestive heart failure. There is some suggestion that anti-TNF drugs increase the risk for lymphomas. Leflunomide. Leflunomide Arava ; blocks autoimmune antibodies and is a powerful anti-inflammatory agent. It is proving to be active against psoriatic arthritis. Reports of adverse effects are comparable to those with methotrexate. Common problems include nausea, diarrhea, hair loss, and rash. Potentially serious side effects include infections and liver injury. Interleukins. Interleukins are other powerful inflammatory agents of the immune system. Interleukins being investigated as sources or targets of therapy include IL-4, IL-2, IL-8, IL-11, and IL-12. For example, in a 2003 study, 75% of patients with severe psoriasis who were treated with interleukin-4 rhuIL-4 ; experienced improvement rates of more than 68 and evista.
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The smiles of Ilana Meallem and Mutassim Abu El Hawa can light up any room. Recently, those smiles and the vital message of the Arava Institute lit up the studios of CNN International. I can proudly say that what you see in that broadcast is what you get when you meet these two engaging Arava alumni in person. Hearing their experiences first-hand made me even more committed to the work we are doing for this unique institution. PROMISE continued on page 2 and fosamax.
| Correspondence: Stacey L. Berg, M.D., Texas Children's Hospital, 6621 Fannin Street, MC3-3320, Houston, TX 77030, USA. Telephone: 713-770-4588; Fax: 713-770-4202. Accepted for publication October 23, 1995. AlphaMed Press 10837159 96 .00 0.
Advantages: 1. Grofit is the hub for manure "production" of the Southern Arava dairy operations. 2. The site is used today for burial of large-scale waste. On the other hand, there are environmental and economic advantages to having various sites throughout the Southern Arava: 1. The prevailing winds are northerly they blow southward ; . 2. The community of Grofit is 1, 200 meters north of the site. Yotvata and public buildings are 3, 000 meters south of the site. On the face of it, it appears that odors are not expected in sensitive-use areas. In addition, the proposal must be checked against the environmental impact statement drafted for the proposed site and rocaltrol.
These 50 drugs represent the most prescribed brand-name drugs that have available generic equivalents. This price list for generic drugs is based on the Maximum Allowable Cost, which applies to various drug card members only. The prices on this list do not show retail prices, so those with other health insurance coverage or without coverage may expect to pay slightly more for generic medications. Also, prices vary between pharmacies so call around to compare drug prices.
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In addition, the notice contains instructions regarding how stockholders may request receipt of proxy materials electronically by e-mail in future years and actonel.
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As discussedabove, we have thoroughly evaluatedthe extensivedata availableto us regarding Arava. On the basisof this review, we have determinedthat, on the whole, thesedata do not demonstrate Arava presentsa risk of serioushepatotoxicity or other that toxicity severeenough, or that it is insufficiently effective, to justify removing this drug from the market.24We will continueto evaluateArava' risk-benefit profile as new s information becomesavailable and will take appropriateregulatory action as needed. However, as explainedabove, currently available scientific information doesnot support.
The Novartis Learning activities in 2002 also helped to build up project leadership skills. A strong project leadership ability is critical in keeping Novartis at the forefront of the fast-paced, highly competitive healthcare industry. The project management curriculum offered more than 600 Novartis managers the unique opportunity to enhance their capability in managing very demanding and complex projects, especially within Research and Development and eulexin.
Cardiovascular Common: Rare: Common: Uncommon: Very rare: Other Common: Weight loss, asthenia Recent, concomitant or consecutive use of potentially myelotoxic agents may be associated with a higher risk of haematological effects. In most reported cases of pancytopenia, SJS and TEN, co-medication was given which is associated with the risk of pancytopenia or SJS or TEN. Very rare cases of severe liver injury, with fatal outcome in isolated cases, have been reported during treatment with ARAVA. This risk may be increased when ARAVA is combined with other DMARDS. Most of the cases occurred within the first 6 months of treatment. Although confounding factors were present in many cases, a causal relationship to leflunomide cannot be excluded. It is considered essential that monitoring recommendations are strictly adhered to. Respiratory, thoracic and mediastinal disorders Nervous system.
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Business is booming for the "clean" fruit. Bell pepper production in Arava Valley has grown a hundred times since the programme started, from less than million a year in 1998 when the programme started to 0 million in exports last year. Pesticide use has fallen. Across the valley in Jordan, Abdullah Ja'afreh sees his fruit farm production rising. He and other growers are exporting to their Gulf neighbours and entering Eastern European markets. Yields have improved and there's better quality fruit for the local market. "The Medfly is not the big problem it once was. Ten years ago you would see infestation on guavas. Now not, " Mr. Ja'afreh says. The IAEA and FAO first helped to set up pilot projects and supply sterile male Medflies to Israel and Jordan in 1998, four years after Israel and Jordan signed a peace treaty and related cooperation agreements. The Palestinian Authority joined the partnership one year later, and now has the capacity to adopt the technology. The IAEA funded the partnership for many years, and so did the USA, including a fouryear, .5 million grant. The sterile flies are bred in a commercial mass-rearing facility in Israel called Biofly. Among the specialists there is Inbar Shouster-Dagan, who was trained on mass-rearing techniques at the IAEA's Seibersdorf Laboratories and in Chile. She says that 20 million sterile male flies are produced there each week for release into the wild. Plans today are to expand the science alliance. In the Gaza Strip, Palestinian fruit growers already have placed bulk orders for sterile Medflies, and hopes are high that the SIT project can resume as political conditions allow. Interest is strong in other areas of Israel and Jordan. In Ashqelon near Gaza, Michael Noy manages fruit and vegetable farms with a 0 million annual turn-over. He also wants to benefit from SIT-based campaigns. "Every year more and more chemicals are banned, " Mr. Noy explains. "Ten years from now there may be no other option. Consumers want quality fruit." Farther north, beyond the Arava Valley in Jordan, the story is much the same. Farmers rely heavily on pesticides to control Medflies and other pests. Even so, Ahmad Mustafa Massadeh complains that the Medfly destroys about 25% of his crop. Mary Bahdousheh coordinates the Medfly project in Jordan, as the Head of Agricultural Pest Control. Unlike the mistrust clouding the Medfly partnership with Israel in the mid-1990s, years of cooperation and communication since then have paid off, she says. With the IAEA's and avodart.
Revenue mil ; .45 Income mil ; .63 ; Assets mil ; .18 Liability mil ; .87 for the year ended 12 31 2006.
3 recent data have raised concerns about the patch's efficacy in women with greater baseline body weight, however and propecia and Cheap arava online.
Acacia trees in the Negev and Arava are in substantial danger of extinction due to high mortality levels up to 60% ; and low recruitment Ashkenazi, 1995; Ward and Rohner, 1997 ; . A major cause of lack of recruitment is infestation of seeds by.
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Or 2. Section 23 Other terms The amount of an ARAVA loan for a right-of-occupancy building as a rental building loan and a loan to purchase a rental building shall be at most 90 per cent of the loan value of the object of the loan. Otherwise, what is prescribed or provided on a rental building loan, a loan to purchase a rental building or a long-term or short-term renovation loan for rental housing shall apply to a right-of-occupancy loan, unless otherwise provided in this or some other act or regulations issued under them.
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Symptoms of an allergic reaction may include a very itchy skin rash.
Obesity linked to risk of pancreatic cancer october 18, 2001 scientists say that maintaining a healthy weight may help reduce the risk of developing this hard-to-treat form of cancer.
There have been reports of chronic overdose in patients taking Arava at daily dose up to five times the recommended daily dose and reports of acute overdose. There were no adverse events reported in the majority of case reports of overdose. Adverse events were consistent with the safety profile for ARAVA. The most frequent adverse events observed were diarrhoea, abdominal pain, leukopenia, anaemia and elevated liver function tests. Management In the event of a significant overdose or toxicity, cholestyramine or charcoal administration is recommended to accelerate elimination. Cholestyramine given orally at a dose of 8 g three times a day for 24 hours to three healthy volunteers decreased plasma levels of A771726 by approximately 40% in 24 hours and by 49 - 65% in 48 hours. Administration of activated charcoal powder made into a suspension ; orally or via nasogastric tube 50 g every 6 hours for 24 hours ; has been shown to reduce plasma concentrations of the active metabolite A771726 by 37% in 24 hours and by 48% in 48 hours and buy didronel.
If you would like to make a contribution, please contact the commission at 501-296-1788 800-459-1517 voice ; 501-296-1794 tdd ; , or send your donation to: ar spinal cord commission 1501 university, suite 470 little rock, ar 72207 new findings in pressure ulcer prevention and treatment pressure ulcers are a common, debilitating and costly complication of sci, often requiring long periods of immobility, hospitalization and or surgery.
In addition to decreases in mean total serum cholesterol in the 39 patient subset, LDL cholesterol was reduced by an average of 14.3%. HDL and VLDL cholesterol, as well as triglycerides, were essentially unchanged from baseline. VGytensin * is not a cholesterollowering agent and is not indicated in the treatment of hyperlipidemia.
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DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug No. Administration 993-01181 of Arava Food Notice. The Food and Drug period Administration for Arava and FDA ; is has determined this made to and Drug Administration, HHS. Regulatory Review Period for Purposes of Patent.
Breast-Ovarian Families From a Breast Cancer Risk Evaluation Clinic, 2247 Martin C, see Isla D Martin CG, see Elting LS Martin PM, see Broet P Martin P-M, see Chinot O-L Martinez A, see Vicini FA Martinez E, see Villafranca E Martinez-Cedillo J, see Campos D Martino B, see Specchia G Martins RG, see Goulart BHL Martone B, see Sosman JA Marty M, see Delaloge S Marty V, see Lee P Marubini E, see Camerini T --see Menard S --see Pizzocaro G Marzullo F, see Paradiso A Mascarenhas B, see van Londen GJ Mascari R, see Kirkwood JM Mascaro JM, see Albanell J Masera G, see Rizzari C Masi G, see Falcone A Maslak P, see Schwartz GK Massarweh S, Dhingra. Unusual Sites of Malignancy; Case 3: Solitary Splenic Metastasis in Lung Cancer Spontaneous Rupture, 1574 Massimino M, Cefalo G, Trecate G, Simonetti F. Pediatric Tumors; Case 1: Sucking and Recovery After Brain Surgery, 273 Masson J, see Guermazi A Massuti B, see Isla D Mataix R, see Sureda A Materazzo C, see Grasselli G --see Zambetti M Mathews J, see Quinn DI Mathur D, see Buchholz TA Matsouka C, see Dimopoulos MA Matthews J, see Lillington DM --see McLachlan S-A Matthews JC, see Saleem A Matulonis U, see Burstein HJ Mauceri G, see Gebbia V Mauch P, see Soiffer RJ Mauch PM, see Backstrand KH.
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