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Mass flow rate liquids ; : Promass A, I, M, F 0.05% [1 2 x zero stability flow rate ; x 100]% of rate Mass flow rate gas ; : Promass A, I, M, F 0.25% [1 2 x zero stability flow rate ; x 100]% of rate Volume flow rate liquids ; : Promass A, M, 0.10% [1 2 x zero stability flow rate ; x 100]% of rate Promass I 0.20% [1 2 x zero stability flow rate ; x 100]% of rate Promass F 0.05% [1 2 x zero stability flow rate ; x 100]% of rate zero stability see table page 127.

Also weigh equally in favor of a finding that jurisdiction and venue are proper in the Eastern District of Tennessee. Thus, Defendant's proposed alternative forum is a place where this action "might have been brought." With regard to the second question, the burden is on the moving party to establish that transfer to another forum is appropriate. Gulf Oil Corp. v. Gilbert, 330 U.S. 501, 67 S. Ct. 839, 843, 91 L. Ed. 1055 1947 ; . See also, Moeckel v. Caremark RX, Inc., 385 F. Supp. 2d 668, 686 M.D. Tenn. 2005 Blane v. Amer. Inventors Corp., 934 F. Supp. 903, 907 M.D. Tenn. 1996 ; . "Unless the balance is strongly in favor of the defendant, the plaintiff's choice of forum should rarely be disturbed." Id. Here, the Court finds that, based on the record before it, a change of venue is not appropriate. There is nothing in the record to indicate that transferring this case to the Eastern District will be more convenient for potential fact witnesses or Plaintiffs' treating physicians. In addition, with the exception of one of the Plaintiffs in the Anderson case out of the thirty-eight Plaintiffs in the three related cases before the Court, there is no evidence that the parties are any closer to the Eastern District than to the Middle District, or that any documentary evidence or other proof is closer to the Eastern District than to the Middle District. Finally, there is no evidence that the situs of material events is any closer to the Eastern District than to the Middle District or that changing venue to the Eastern District will make the parties' ability to bear the expense of litigation any easier. Thus, the totality of the factors to be considered in this decision do not clearly justify a change of venue. Deciding whether to transfer a case is within the sound discretion of the Court to be exercised in light of all the circumstances of a case. Phelps, 30 F. 3d 658, 663 Cir. 1994.

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Step Therapy Step Therapy promotes appropriate utilization of first-line drugs and or therapeutic categories. Step Therapy requires that participants receive one or more first-line drug s ; , as defined by program criteria before prescriptions are covered for second-line drugs in defined cases where a step approach to drug therapy is clinically justified. To promote use of cost-effective first-line therapy, PEIA uses step therapy in the following therapeutic classes: Angiotensin-Converting Enzyme ACE ; Inhibitors Accuretic, Accupril, Aceon, Altace, Capoten Capozide, Lexxel, Lotesin HCT, Lotrel, Mavik, Monopril HCT, Prinivil, Prinizide, Tarka, Uniretic, Univasc, Vasotec, Vaseretic ; Angiotensin II Receptor Antagonists Atacand HCT, Teveten HCT, Avapro, Cozaar, Benicar HCT, Micardis HCT, Diovan HCT, Avalide, Hyzaar ; Disease-modifying Antirheumatic Drugs e.g., Enbrel, Kineret, Humira ; Inspra Leukotriene Inhibitors e.g., Accolate, Singulair, Zyflo ; Non-Steroidal Anti-inflammatory Drugs brand-name NSAID e.g., Celebrex, Vioxx, Arthrotec, Bextra, Mobic ; , Proton Pump Inhibitors e.g., Prilosec, Prevacid, Nexium, Aciphex, Protonix ; , Selective Serotonin Reuptake Inhibitors e.g., Celexa, Lexapro, Luvox, Paxil, Paxil CR, Prozac, Prozac Weekly, Zoloft ; , Straterra Xopenex This list is subject to change during the plan year, if circumstances arise which require adjustment. Changes will be communicated to members through the PEIA News. The changes will be included in PEIA's Plan Document, which is filed with the Secretary of State's office, and will be incorporated into the next edition of the Summary Plan Description. Quantity Limits Under the PEIA PPB Plan Prescription Drug Program, certain drugs have preset coverage limitations quantity limits ; . Quantity limits ensure that the quantity of units supplied in each prescription remains consistent with clinical dosing guidelines and PEIA's benefit design. Quantity limits encourage safe, effective and economic use of drugs and ensure that members receive quality care. Select medications from the quantity limit list are provided on the list starting below. If you are taking one of the medications listed below and you need to get more of the medication than the plan allows, ask your pharmacist or doctor to call Express Scripts to discuss your refill options. Anzemet, Emend, Kytril, Zofran coverage limitations: Anzemet is limited to 1 tablet per prescription Emend 80mg is limited to 2 capsules per prescription. Emend 125mg is limited to 1 capsule per prescription. Emend Tri-fold Pack is limited to 1 package per prescription. Kytril is limited to 2 tablets per prescription Zofran 24 mg is limited to 1 tablet per prescription Zofran 4 mg and 8 mg are limited to 12 tablets per prescription Zofran Solution is limited to 3 bottles per prescription.

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Nefort Parisiensis in Lusitanicis suis perambulationibus feliciter detexit". In Tournefort's herbarium there is a specimen n. 6443 ; which bears the above label "Orobanche elegantissima verna flore lteo virid. Lusit. Grisley" and whose identity corresponds to what is currently known as Cistanche phelypaea. This is now designated the neotype. Cz, the different to avoid benicar providers paying narcan be quantified factors and benztropine.
Ations in hCG LH titers in her serum 8 ; . The patient had no previous exposure to hormone therapy. We describe a case of a 30-yr-old woman with unexplained infertility who has developed a neutralizing antibody to hCG that appeared to be maintained by repeated exposure to exogenous and endogenous hCG. This interfered with in vitro fertilization IVF ; treatment by blocking the action of exogenous hCG. Emergency training required certificates: Paid Coach Only-copy of card must be sent in ; First Aid Certification American Red Cross or other accredited association ; CPR Certification American Red Cross, American Heart Assoc., or other accredited assoc. ; Water Safety Instructor Certification Swimming Coach Only ; Lifeguard Certification Swimming Coach Only ; Human Resources Requirements: All Coaches ; TB Test Negative Result within last four years-copy of results must be sent in ; Fingerprinting Must be done through SFUSD HR Dept. ; Coaching Education Requirements: Paid High School Coach Only ; ASEP or NFHS Required after first year of paid coaching ; ASEP NFHS Waiver First year paid coaches only ; Coaching theory and techniques in the sport being coached, evidenced by: Paid Coach Only ; Prior services as an assistant athletic coach in the sport to be coached Program Name Prior work in a community youth athletic program Program Name Completion of a college level course in coaching theory and the techniques of sport: College University Prior participation in organized competitive athletics at the high school level or above and bepridil. P.V. Plazas et al. European Journal of Pharmacology xx 2007 ; casino online secret system winningx 5. Pretreatment counts averages of at least 2 measurements not influenced by 1 week apart and betaseron. Patients with androgen-independent prostate cancer fall into three broad categories: biochemical-only disease, asymptomatic disease with positive scans, and symptomatic disease Figure 5 ; . The variability of the natural history of the disease in these categories raises several major questions: who should be treated, when should they be treated, and how should they be treated? A patient with a rising PSA despite hormonal therapy should undergo staging with a physical exam, bone scan, and computed tomography scan of the abdomen pelvis. If they have biochemical-only disease, a decision must be made as to whether to treat these patients or to follow them. This first decision can be based, at least partially, on the speed at which the PSA is doubling PSADT ; as well as other factors such as patient age and overall health. Patients with slow doubling times 8 to 12 months ; are suitable for monitoring. Bone scans can be performed every six months or on a yearly basis. Patients with.

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No data were available across any health state for 5 of 959 patients. Table 1 shows the distribution of patients in each health state, according to treatment group, at baseline. State 2 moderate ; had the greatest number of patients. For the initial baseline period, there was no significant difference in the distribution of health states across treatment groups P .45 and betaxolol.
Bourgain, C., Smitz, J., Vandesteen, N. et al. 1992 ; Endometrial estrogen and progesterone receptors in cycles treated for infertility. Prog. Histochem. Cytochem., 26, 132139. Bourgain, C., Smitz, J., Camus, M. et al. 1994 ; Human endometrial maturation is markedly improved after luteal supplementation of gonadotrophin-releasing hormone analogue human menopausal gonadotrophin stimulated cycles. Hum. Reprod., 9, 3240. Bulletti, C., de Ziegler, D., Flamigni, C. et al. 1997 ; Targeted drug delivery in gynaecology: the first uterine pass effect. Hum. Reprod., 12, 10731079. Buvat, J., Marcolin, G., Guittard, C. et al. 1990a ; Luteal support after luteinizing hormone-releasing hormone agonist for in vitro fertilization: superiority of human chorionic gonadotropin over oral progesterone. Fertil. Steril., 53, 490494. Buvat, J., Marcolin, G., Guittard, C. et al. 1990b ; Sutien lutal apres LHRHagonistes pour fcondation in vitro: La progesterone vaginale est suprieure la progesterone orale, et aussi efficace que la gonadotrophine chorionique hCG ; Contracept. Fertil. Sex., 18, 616617. Casanas-Roux, F., Nisolle, M., Marbaix, E. et al. 1996 ; Morphometric, immunohistological and three-dimensional evaluation of the endometrium of menopausal women treated by oestrogen and Crinone, a new slowrelease vaginal progesterone. Hum. Reprod., 11, 357363. Chakmakjian, Z.H. and Zacharian, N.Y. 1987 ; Bioavailability of progesterone with different modes of administration. J. Reprod. Med., 32, 443448. Check, J.H., Rankin, A. and Teichman, M. 1986 ; The risk of fetal anomalies as a result of progesterone therapy during pregnancy. Fertil. Steril., 45, 575577. Chez, R.A. 1978 ; Proceedings of the symposium "progesterone, progestins and fetal development". Fertil. Steril., 30, 1626. Cicinelli, E., Cignarelli, M., Resta, L. et al. 1993 ; Effects of the repetitive administration of progesterone by nasal spray in postmenopausal women. Fertil. Steril., 60, 10201024. Cicinelli, E., Nahoul, K., Petruzzi, D. et al. 1994 ; Nasal spray administration of unmodified progesterone: evaluation of progesterone serum levels with three different radioimmunoassay techniques. Maturitas, 19, 4352. Cicinelli, E., Borraccino, V., Petruzzi, D. et al. 1996 ; Pharmacokinetics and endometrial effects of the vaginal administration of micronized progesterone in an oil-based solution to postmenopausal women. Fertil. Steril., 65, 860862. Cicinelli, E., Cignarelli, M., Sabatelli, S. et al. 1998 ; Plasma concentrations of progesterone are higher in the uterine artery than in the radial artery after vaginal administration of micronized progesterone in an oil-based solution to postmenopausal women. Fertil. Steril., 69, 471473. Claman, P., Domingo, M. and Leader, A. 1992 ; Luteal phase support in invitro fertilization using gonadotrophin releasing hormone analogue before ovarian stimulation: a prospective randomized study of human chorionic gonadotrophin versus intramuscular progesterone. Hum. Reprod., 7, 487 489. Critchley, H., Buckley, C.H. and Anderson, D. 1990 ; Experience with a `physiological' steroid replacement regimen for the establishment of a receptive endometrium in women with premature ovarian failure. Br. J. Obstet. Gynaecol., 97, 804810. Davies, M.C., Anderson, M.C., Mason, B.A. et al. 1990 ; Oocyte donation: the role of endometrial receptivity. Hum. Reprod., 5, 862869. Daya, S. 1988 ; Efficacy of progesterone support in the luteal phase following in-vitro fertilization and embryo transfer: a meta-analysis of clinical trials. Hum. Reprod., 3, 731734. Deaton, J.L., Clark, R.R., Pittaway, D.E. et al. 1997 ; Clomiphene citrate ovulation induction in combination with a timed intrauterine insemination: the value of urinary luteinizing hormone versus human chorionic gonadotropin timing. Fertil. Steril., 68, 4347. Dehou, M.-F., Lejeune, B., Arijs, C. et al. 1987 ; Endometrial morphology in stimulated in vitro fertilization cycles and after steroid replacement therapy in cases of primary ovarian failure. Fertil. Steril., 48, 9951000. Dennerstein, L., Burrows, G.D., Hyman, G.J. et al. 1979 ; Hormone therapy and affect. Maturitas, 1, 247259. Devroey, P., Braeckmans, P., Camus, M. et al. 1988 ; Embryo donation in patients with primary ovarian failure. Hum. Reprod., 3 Suppl. 2 ; , 8587. Devroey, P., Palermo, G., Bourgain, C. et al. 1989 ; Progesterone administration in patients with absent ovaries. Int. J. Fertil., 34, 188193. De Ziegler, D., Bergeron, C., Cornel, C. et al. 1992 ; Effects of luteal estradiol on the secretory transformation of human endometrium and plasma gonadotropins. J. Clin. Endocrinol. Metab., 74, 322331.

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Were promises made by the Crown to its allies, including ancestors of the Moose Deer Point First Nation? The first issue in this inquiry involves questions of fact more than of law namely, whether statements made by the Crown amounted to promises to its allies, and, if so, whether the allies to whom those promises were directed included ancestors of the Moose Deer Point First Nation. Our task is made easier by the following concession made by the Crown in its written submission: The evidence indicates that these Pottawatomi came to Canada after the War of 1812 for several reasons, including: actions taken by the Americans to move the Indians west; because they "did not dare to return" ICC Doc. 104-105 in the hope of avoiding forcible assimilation into non-native culture ICC Exhibit 9, at 18 and because of promises by the British that if they came to Upper Canada they would be "treated the same as other Indians." ICC Doc. 419 ; One group eventually settled at Moose Deer Point. ICC Doc. 38-39 ; Page 15 of the historical report prepared by Joan Holmes & Associates, Inc. in 1994 ICC Exhibit 2 ; lists various members of the King family who completed applications for band membership, or who were listed in reports of non-treaty Indians residing on reserves. The report compares the names of the applicants, and the names of siblings and parents, with lists of individuals and families residing at Moose Deer Point, and concludes that the group of Indians residing at Moose Deer Point were descended from Chief Ogemahwahjwon, who had fought for the British in the War of 1812, and that they were descendants of the Pottawatomi who migrated to Canada in the 1830's or 1840's. Despite various inconsistencies and gaps in the historical record, for the purposes of this inquiry Canada accepts this conclusion as accurate. Although there is no evidence that ancestors of the Moose Deer Point First Nation were present at the 1837 council at Manitouwaning [sic], there is evidence indicating that similar promises were likely made to the First Nation's ancestors at another council, probably in 1836, the last year presents were distributed at Macinac [sic] Island.305 and bevacizumab. Waist measurement at the narrowest point ; divided by hip measurement at the widest point ; . Weight carried around the waist an "apple" shape ; is associated with greater cardiovascular risk than weight distributed around the hips and thighs a "pear" shape ; . A healthy waist-to-hip ratio is below 0.9 for men or 0.8 for women. This measure may not be appropriate for HIV positive individuals with lipodystrophy and benicar. Sklarek, J, Mantovani, R, Erens, E, Heisler, D, Niederman, MS, Fein, AM: AIDS in a bodybuilder using anabolic steroids. New England Journal of Medicine 1984; 311 26 ; : 1701 letter ; . Niederman, MS: When is bronchoscopy indicated for diagnosis of tuberculosis? The Journal of Respiratory Diseases 1993; 14 7 ; : 815 letter ; . Niederman, MS, Fein, AM, Feinsilver, SH, Ilowite, JI: Benefits of a multidisciplinary pulmonary rehabilitation program. Chest 1994; 105 2 ; : 641 letter ; . Niederman MS: Chest films, pneumonia diagnosis, and maternal and fetal well-being. Consultant 1995; 35 6 ; : 781 letter ; . Niederman, MS, Mandell, LA: Current Concepts: CommunityAcquired pneumonia. New England Journal of Medicine 1996; 334 13 ; : 861. Niederman, MS: Gram's stains and cultures: What role in managing VAP? The Journal of Critical Illness 1998; 13 2 ; : 80-81. Niederman, MS: Editorial response to article- Update in pulmonary disease Annals of Internal Medicine 1998; 128 3 ; : 208-215 ; . Annals of Internal Medicine 1998; 129 6 ; : 510. Niederman, MS: Community-acquired pneumonia commentary- Outpatient Treatment is safe for low risk pneumonia cases. Pulmonary Reviews 1998; 3 7 ; : 60. Echols, RM, Fink MP, Snydman DR, Niederman MS: Antimicrobial Agents and Chemotherapy. In press 1995 letter and bexarotene.

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MARIANO MARCOS STATE UNIVERSITY-BATAC MATS COLLEGE OF TECHNOLOGY MEIN COLLEGE INC.-ZAMBOANGA CITY MINDANAO ELECTRONICS INSTITUTE-SCHOOL OF MIDWIFERY MINDANAO POLYTECHNIC STATE COLLEGE DMMMPSC ; MINDANAO STATE UNIVERSITY-ILIGAN INSTITUTE OF TECHNOLOGY MINDANAO STATE UNIVERSITY-MARAWI CITY MISAMIS INSTITUTE OF TECHNOLOGY NATIONAL COLLEGE OF SCIENCE & TECHNOLOGYDASMARINAS NATIONAL COLLEGE OF SCIENCE & TECHNOLOGY-SAN FERNANDO NATIONAL UNIVERSITY NEGROS ORIENTAL STATE UNIVERSITY CVPC ; DUMAGUETE NEW ERA UNIVERSITY NORTHWESTERN UNIVERSITY NOTRE DAME OF DADIANGAS COLLEGE NOTRE DAME OF KIDAPAWAN COLLEGE NOTRE DAME OF MARBEL UNIVERSITY NOTRE DAME UNIVERSITY NUEVA VIZCAYA STATE UNIVERSITY- NVPC ; BAMBANG OUR LADY OF THE PILLAR'S COLLEGE PAMANTASAN NG LUNGSOD NG MAYNILA PAMANTASAN NG LUNGSOD NG PASIG PANGASINAN COLLEGE OF SCIENCE & TECHNOLOGY PATRIA SABLE CORPUZ COLLEGE PHILIPPINE COLLEGE OF SCIENCE & TECHNOLOGYCALASIAO POLYTECHNIC STATE COLLEGE OF ANTIQUE POLYTECHNIC UNIVERSITY OF THE PHILIPPINESBATAAN POLYTECHNIC UNIVERSITY OF THE PHILIPPINES-MAINSTA. MESA POLYTECHNIC UNIVERSITY OF THE PHILIPPINESMARAGONDON POLYTECHNIC UNIVERSITY OF THE PHILIPPINES-STO. TOMAS POLYTECHNIC UNIVERSITY OF THE PHILIPPINESTAGUIG RIZAL TECHNOLOGICAL UNIVERSITY SAINT FRANCIS OF ASSISSI COLLEGE SAINT JOHN TECHNOLOGICAL COLLEGE OF THE PHILIPPINES SAINT JOSEPH INSTITUTE OF TECHNOLOGY SAINT LOUIS UNIVERSITY SAINT MARY'S UNIVERSITY SAINT PAUL UNIVERSITY-TUGUEGARAO SAINT PETER'S COLLEGE-ILIGAN CITY SAINT VINCENT COLLEGE-DIPOLOG CITY SAMAR STATE UNIVERSITY SAMAR S.P.C. ; SAN SEBASTIAN COLLEGE-RECOLETOS SOUTHERN LUZON POLYTECHNIC COLLEGE-LUCBAN SYSTEMS PLUS COLLEGE FOUNDATION, INC-ANGELES CITY SPCCF ; TECHNOLOGICAL INSTITUTE OF THE PHILIPPINESMANILA TECHNOLOGICAL INSTITUTE OF THE PHILIPPINESQUEZON CITY TECHNOLOGICAL UNIVERSITY OF THE PHILIPPINESMANILA TECHNOLOGICAL UNIVERSITY OF THE PHILIPPINESTAGUIG TECHNOLOGICAL UNIVERSITY OF THE PHILIPPINESVISAYAS.
Distinct signal transduction pathways. J Immunol. 1991; 146: 846-853. Semac I, Palomba C, Kulangara K, et al. AntiCD20 therapeutic antibody rituximab modifies the functional organization of rafts microdomains of B lymphoma cells. Cancer Res. 2003; 63: 534-540. Hofmeister JK, Cooney D, Coggeshall KM. Clustered CD20 induced apoptosis: src-family kinase, the proximal regulator of tyrosine phosphorylation, calcium influx, and caspase 3-dependent apoptosis. Blood Cells Mol Dis. 2000; 26: 133-143. Bezombes C, Grazide S, Garret C, et al. Rituximab antiproliferative effect in B lymphoma cells is associated with acid-sphingomyelinase activation in raft microdomains. Blood. 2004; 104: 11661173. O'Keefe TL, Williams GT, Davies SL, Neuberger MS. Mice carrying a CD20 gene disruption. Immunogenetics. 1998; 48: 125-132. Li H, Ayert LM, Lytton J, Deans JP. Store-operated cation entry mediated by CD20 in membrane rafts. J Biol Chem. 2003; 278: 42427-42434. Bourget I, Di Berardino W, Breittmayer JP, et al. CD20 monoclonal antibodies stimulate extracellular cleavage of the low affinity receptor for IgE Fc epsilon RII CD23 ; in Epstein-Barr-transformed B cells. J Biol Chem. 1994; 269: 6927-6930. Bourget I, Breittmayer JP, Grenier-Brossette N, Cousin JL. CD20 monoclonal antibodies downregulate IgM at the surface of B cells. Eur J Immunol. 1993; 23: 768-771. Flieger D, Renoth S, Beier I, Sauerbruch T, Schmidt-Wolf I. Mechanism of cytotoxicity induced by chimeric mouse human monoclonal antibody IDEC-C2B8 in CD20-expressing lymphoma cell lines. Cell Immunol. 2000; 204: 55-63. Shan D, Ledbetter JA, Press OW. Signaling events involved in anti-CD20-induced apoptosis of malignant human B cells. Cancer Immunol Immunother. 2000; 48: 673-683. Mathas S, Rickers A, Bommert K, Dorken B, Mapara MY. Anti-CD20- and B-cell receptor-mediated apoptosis: evidence for shared intracellular signaling pathways. Cancer Res. 2000; 60: 71707176. Golay J, Zaffaroni L, Vaccari T, et al. Biologic response of B lymphoma cells to anti-CD20 monoclonal antibody rituximab in vitro: CD55 and CD59 regulate complement-mediated cell lysis. Blood. 2000; 95: 3900-3908. Valentine MA, Licciardi KA. Rescue from antiIgM-induced programmed cell death by the B cell surface proteins CD20 and CD40. Eur J Immunol. 1992; 22: 3141-3148. Shan D, Ledbetter JA, Press OW. Apoptosis of malignant human B cells by ligation of CD20 with monoclonal antibodies. Blood. 1998; 91: 16441652. Genestier L, Bonnefoy-Berard N, Rouault JP, Flacher M, Revillard JP. Tumor necrosis factor-alpha up-regulates Bcl-2 expression and decreases calcium-dependent apoptosis in human B cell lines. Int Immunol. 1995; 7: 533-540. Hockenbery DM, Oltvai ZN, Yin XM, Milliman CL, Korsmeyer SJ. Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell. 1993; 75: 241251. Baffy G, Miyashita T, Williamson JR, Reed JC. Apoptosis induced by withdrawal of interleukin-3 IL-3 ; from an IL-3-dependent hematopoietic cell line is associated with repartitioning of intracellular calcium and is blocked by enforced Bcl-2 oncoprotein production. J Biol Chem. 1993; 268: 6511-6519. Byrd JC, Kitada S, Flinn IW, et al. The mechanism of tumor cell clearance by rituximab in vivo in patients with B-cell chronic lymphocytic leukemia: evidence of caspase activation and apoptosis induction. Blood. 2002; 99: 1038-1043. Lieberman J. The ABCS of granule-mediated cy and bidil.

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