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Patients and methods : the opera overactive bladder: performance of extended release agents ; trial was a randomized, double-blind, active-control study performed at 71 us study centers from november 21, 2000, to october 18, 200 extended-release formulations of oxybutynin at 10 mg d or tolterodine at 4 mg d were given for 12 weeks to women with 21 to 60 urge urinary incontinence uui ; episodes per week and an average of 10 or more voids per 24 hours.

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Wyeth and Progenics Pharmaceuticals have shifted their intravenous form of the opioid antagonist methylnaltrexone into Phase III trials for post-operative ileus. The condition refers to a lack of passage due to paralysis of the bowel and currently has no effective pharmaceutical treatment -- further surgery is the only option. The study, approved under an FDA Special Protocol Assessment and granted Fast Track status this quarter, will involve 500 patients undergoing segmental colectomy. If the outcome is promising, analysts suggest sales of $220 million by 2012. In this issue of the Journal, Drs Bernie Brenner and Michael Rice : nzma .nz journal 119-1229 1846 ; discuss the funding of tolterodine Detrusitol ; for overactive bladder. In 1999 Pharmacia & Upjohn--now Pfizer Pharmaceuticals Group--submitted a proposal for the listing of tolterodine on the Pharmaceutical Schedule for patients who are intolerant or non-responsive to a course of oxybutynin. The application was considered twice by the Pharmacology and Therapeutics Advisory Committee PTAC ; that same year. After initially recommending the application be declined, PTAC eventually recommended that tolterodine be listed but with a low priority. PTAC considered that the price asked for tolterodine was too high for the limited additional benefit in tolerability over oxybutynin. In general, applications with low priority PTAC recommendations are treated with less urgency than higher priority recommendations. PHARMAC and the supplier were unable to reach agreement over the listing of tolterodine. Pfizer did not respond to a letter from PHARMAC sent in July 2003 signalling an intention to recommend that the application be declined. PHARMAC subsequently declined the application in January 2005. * A decision to decline an application does not necessarily prevent further contractual arrangements at a later date; it does however clearly indicate to suppliers that PHARMAC is no longer progressing the application at this stage. This study compared the risk of adverse pregnancy outcomes for the second birth between 31683 women from Norway who changed partners between their first and second births and 456458 women with the same partner for both births. After adjusting for age, education, interval between births and other confounding variables, these researchers report an increased risk for preterm delivery, low birth weight and infant mortality in those women who changed partners as opposed to those who had the same partner for both births. The hypothesis that the authors put forward is that the change in lifestyle and an increase in less healthy lifestyle smoking, alcohol ; are most likely responsible for the difference.

Anatomical changes in the frontolimbic areas of the brain e.g., the orbitofrontal cortex, anterior cingulate, and gyrus rectus ; have recently been associated with depression, including white-matter hyperdensities and an increased volume of cerebrospinal fluid CSF ; .3335 The severity of the Table 1 Definition of Depression * hyperdensities, especially those involving the amygdala and periventricular region, correlates with the degree of depression and cognitive prob1. Depressed mood most of the day nearly every day, as indicated by lems36, 37 and may also help to predict treatmenteither subjective report e.g., feels sad or empty ; or observation refractory or unstable depression.30, 38 White-matter made by others e.g., appears tearful ; . lesions are more significant in men with late-onset 2. Markedly diminished interest or pleasure in all anhedonia ; , or depression.39, 40 Gray matter decreases in patients almost all activities most of the day, nearly every day as indicated by with early-onset depression.19, 33, 41 either subjective account or observation made by others ; Cerebrovascular lesions in the region of the stri3. A significant weight loss when not dieting or weight gain e.g., a atopallidothalamocortical pathways and other change of more than 5% of body weight in a month ; , or decrease or areas have been associated with depression, cogniincrease in appetite nearly every day. tive problems, apathy, and lack of insight.16, 31 There 4. Insomnia or hypersomnia nearly every day. is growing evidence that late-onset depression in 5. Psychomotor agitation or retardation nearly every day observable the "oldest old" population is linked to cardiovascuby others, not merely subjective feelings of restlessness or being lar and cerebrovascular burden.10, 31, 42 slowed down ; . Elevated cor ticosteroids activate the hypo6. Fatigue or loss of energy nearly every day. thalamicpituitaryadrenal H-P-A ; axis, deregu7. Feelings of worthlessness or excessive or inappropriate guilt which late the serotonergic system, and are associated may be delusional ; nearly every day not merely self-reproach or with hippocampal atrophy, cognitive impairment, guilt about being sick ; . and depression.8, 13, 18, 43, It is well recognized that 8. Diminished ability to think or concentrate, or indecisiveness, nearly depression is included in the differential diagnosis every day either by subjective account or as observed by others ; . for dementia in the elderly.45 9. Recurrent thoughts of death not just fear of dying ; , recurrent suicidal ideation without a specific plan, or a suicide attempt or a specific plan for committing suicide. Diagnosis 10. The symptoms do not meet the criteria for a Mixed Episode. The possibility of depression is always present in 11. The symptoms cause a clinically significant distress or impairment in the clinical encounter. The rate at which primary social, occupational, or other important areas of functioning. health care providers recognize clinical depression 12. The symptoms are not due to the direct physiological effects of a varies widely: from 19% to 94%.25 Cognitive impairsubstance e.g., a drug of abuse, or a medication ; or a general medment and other medical comorbidities often hinder ical condition e.g., hypothyroidism ; . the ability to arrive at an accurate diagnosis.46 Yet 13. The symptoms are not better accounted for by bereavement i.e., elderly patients overwhelmingly prefer the care of after loss of a loved one the symptoms persist for longer than two their primary physician to that of a mental health months or as characterized by marked functional impairment, morprofessional. With the advent of managed care bid preoccupation with worthlessness, suicidal ideation, psychotic plans, this trend is expected to increase. There is symptoms, or psychomotor retardation. little to no relationship between the rate of recog * As defined by the Diagnostic and Statistical Manual of Mental Disorders DSM-IV ; . nition by health care clinicians and the rate of treatAdapted from Almeida OP, Almeida SA: Int J Geriatr Psychiatry 1999; 14: 858865.50 ment or referral.3 and gliclazide. It stated: the problems with case reports and adverse drug experience reports were acknowledged by dr. DETROLLA DE-trol el-ay ; tolterodine tartrate extended release capsules ; Read the Patient Information that comes with DETROL LA before you start using it and each time you get a refill. There may be new information. This leaflet does not take the place of talking with your doctor about your condition or your treatment. Only your doctor can determine if treatment with DETROL LA is right for you and dibenzyline.
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TABLE I Genes That Are Specifically Upregulated by Insulin-like Growth Factor-1 in NIH-3T3 Fibroblasts Symbol Mitogenesis and differentiation Interleukin 3 receptor, -chain Colony stimulating factor, macrophage Glial cell line-derived neurotrophic factor Integrin -5 fibronectin receptor ; Early growth response-1 Jun oncogene Twist gene homolog Forkhead homolog 14 Wee 1-like protein kinase Insulin-like growth factor binding protein 10 Sex-determining region Y SRY ; -box containing gene 2 Interleukin 4 receptor alpha Mouse mRNA for dbpa murine homolog Expressed sequence tags, moderately similar to MAK16 S. cerevisae ; Ngfi-A binding protein 2 MAD mothers against decapentaplegic ; homolog 5 Drosophila ; Early development regulator Ets variant gene 6 TEL oncogene ; Apoptosis Mus musculus TDAG51 T-cell deathassociated gene ; Mus musculus Fas-binding protein Daxx ; Cellular processes Murine mRNA for replacement variant histone H3.3 Kinesin heavy chain member 1A Mouse chromatin nonhistone high-mobility group protein HMG-I Y vH3.3 Kin1A HMG-1 Y ; 618380 492514 616054 TDAG51 Daxx 694076 736796 9.00 IL-3R mCSF GNDF I 5 EGR-1 JUN TWIST FKH-14 Wee-1 IGF-BP10 SRY-2 IL-4R DBPA MAK16 NGFI-A BP-2 MAD5 EDR TEL 445664 634838 425671 Clone number IGF-1 Insulin and phenoxybenzamine. Preclinical studies using porcine and human detrusor muscle strips demonstrated that trospium chloride was many-fold more potent than oxybutynin and tolterodine in inhibiting contractile responses to carbachol and electrical stimulation.

There are thousands of healthy hiv-positive people who don't take the drugs, who rely on natural regimens to support their immune function and phenytoin. The calculation of inflation is based on the AWP for each unit of a given product as reported on the day each prescription was filled. AWP was discounted by 12% for brands and 36% for generics. The inflation rate represents the difference between the weighted average discounted AWP per unit in 2003 for common drugs, while holding constant product market share, units per prescription and the brand generic ratio. The inflation rate of 6.9% for 2003 was slightly lower than the 7.5% reported last year. Therapy class inflation rates ranged from a high of 19.2% for estrogens to only 3% for antihistamines. Ironically, when ranked by drug cost rather than by number of prescriptions, estrogens were first last year with an inflation rate of 12.2%, and antihistamines were second at 11.8%. This disparity points out different strategies used by pharmaceutical manufacturers to cope with declining utilization. While manufacturers of estrogens apparently tried to preserve profits as their products fell out of favor, manufacturers of antihistamines kept prices in check, perhaps to remain competitive with OTC alternatives. As seen in previous years, the 7.6% inflation rate for brands far exceeded the generic inflation rate of 3.3%, even though the brand rate was slightly lower than last year. Generic inflation increased only slightly from the 3.1% reported last year. For one, to confirm the woman's ID. Second, you might know our John Doe. And finally, to give us your medical opinion." "My opinion?" I said in a monotone. "You'll get far more from the CSI team and the forensic pathologist." "Ever since that hit TV series, those CSI guys are insufferable." Helen chuckled. "Besides, maybe you can add something. You see a lot of stabbings, don't you?" "One or two." "Can you drop by here on your way home? The address is--" "I know the address." After all, I had once lived there, too and valsartan. | OII-B-1: Population Pharmacokinetic Analysis of Atomoxetine in Pediatric Patients J. Witcher, PhD, D. Kurtz, MS, M. Heathman, MS, J. Sauer, PhD, B. Smith, PhD, Eli Lilly and Company, Indianapolis, IN | OII-B-2: Efficacy, Safety and Pharmacokinetics of Levocetirizine in Allergic Children Aged 1-2 Years N. E. Cranswick, MD, M. Fuchs, MD, J. Turzikova, MD, Royal Children's Hospital, Bulovka Hospital, Parkville, Australia | OII-B-3: Tol6erodine TOL ; Prolonged Release PR ; in Children Aged 11-15 Years D. L. Blowey, MD, S. Abdel-Rahman, W. S. Bundrick, R. Jayanthi, P. Reddy, D. Rivas, M. Borin, N. Borgstein, Children's Mercy Hospitals & Clinics, Pfizer Global Research & Development, Kansas City, MO | OII-B-4: Pharmacokinetics of Methotrexate in Infants with Acute Lymphoblastic Leukemia P. Thompson, MD, Z. E. Dreyer, MD, S. Blaney, MD, S. Berg, MD, D. Murry, PharmD, L. Bomgaars, MD, Texas Children's Hospital, Houston, TX. Gen 31 ; . Similarly, in this study, we did not detect any decrease in serum CH50 levels 6 h after the third i.t. Ag exposure compared with the control saline i.t. ; , suggesting that there was no definite involvement of systemic complement activation during LAR development in this model. After the three repetitions of Ag challenge, we noted that the LAR was associated with a cellular infiltration of the bronchial submucosa that consisted predominantly of eosinophils and neutrophils. Similarly, in a previous report on dermal challenge with allergens in human allergic subjects, it was shown that a triple, but not a double, repetition of Ag exposure led to augmented LAR and increased cellular infiltration in the dermis 11 ; . We then attempted to assess the involvement of complement activation in the airway responses after repeated Ag challenge using two complement inhibitors, Futhan and sCR1 19, 20 ; . Both inhibitors suppressed IAR after single or double exposure to OA but not after triple exposure. In contrast, both inhibitors suppressed LAR and cellular infiltration after the third exposure. When the contribution of C5a to LAR was examined using a C5aRA, LAR, and cellular infiltration of the bronchial submucosa were simultaneously inhibited 22 ; . Taken together, these results suggest that endogenous production of C5a through local complement activation in the airway system after an Ag-Ab reaction might be causally related to the development of LAR. Because LAR has been considered to be intimately associated with symptomatic asthma and to be related to cellular infiltration of the bronchial submucosa and because drugs that inhibit LAR may have a potent antiinflammatory effect in the treatment of asthma, the results of the present study suggest that, in future, anticomplementary drugs may prove to be effective in antiasthmatic therapy 32 ; . Results of Northern hybridization revealed that C5aR mRNA was up-regulated in lungs after the triple OVA exposure, whereas C3aR up-regulation was hardly detected, similar to the results of a previous report using LPS stimulation 27 ; . However, we did not have a definite explanation for the different regulation between C5aR and C3aR mRNAs. This up-regulation of C5aR was inhibited by pretreatment with sCR1 or C5aRA. OVA exposure resulted in increased expression of cytokine and chemokine mRNAs including IL-4, IL-5, eotaxin, and IFN- ; however, complement inhibition or the blocking of C5aR resulted in decreased levels of these cytokines and chemokine in the lungs. The IL-12 message from lungs after the third exposure to Ag was reduced after pretreatment with a complement inhibitor or C5aRA and nevirapine.

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Immediate release oxybutynin versus tolterodine Four DB studies compared the effectiveness of oxybutynin and tolterodine, in men and women predominantly women; 6777% ; with OAB. Duration of treatment ranged from 8 to 12 weeks.349, 350, 385, 386 Across the studies, between 27% and 60% of the study populations had previously received drug treatment for OAB or urge UI. The response to treatment in these groups was not considered separately in the study reports. Two of the four RCTs compared tolterodinee 2 mg b.d. with oxybutynin 5 mg b.d. starting at a lower dose of 2.5 mg b.d. ; . The primary outcome of dry mouth occurred in significantly more oxybutynin-treated patients than with tolterodune 61% versus 37% ; . No significant differences were seen between groups in efficacy outcomes n 378 ; .386 [EL 1 + ] study in Asian patients reported similar findings n 228 ; .385 [EL 1 + ] Two placebo-controlled RCTs of identical design compared toltterodine 2 mg b.d. with oxybutynin 5 mg t.d.s., although one only reported efficacy data for completers 53% of those randomised ; . Both found no significant differences between treatments in frequency or in leakage episodes, while significantly more people treated with oxybutynin reported dry mouth. Improvements in efficacy outcomes were significantly greater with tolterodine and oxybutynin compared with placebo n 293 ; , 349 [EL 1 + ] 277; 147 analysed ; .350 [EL 1-] Following completion of these two studies and two other RCTs ; , patients were offered continued open treatment with tolterodine 2 mg b.d. for a further 9 months.394 Overall 70% continued treatment, with 13% reducing the dose to 1 mg b.d. Reasons stated for withdrawal were adverse events 9% ; , lack of efficacy 6% ; , loss to follow-up or withdrew consent 10% ; . Bladder diary variables indicated sustained benefit in those who continued treatment. Dry mouth was the most common adverse effect 28% ; .394 [EL 3] Two open RCTs with specific objectives provide further comparative data for tolterodine and oxybutynin in women with OAB. Duration of treatment was 1012 weeks; one was a crossover study.387, 388 The main objective of one study was to assess whether urodynamic grade predicts response to treatment; this also reported no differences between tolterodine 2 mg b.d. and oxybutynin 5 mg t.d.s. in frequency or cystometric capacity n 128; 107 analysed ; .387 [EL 1-] The other RCT evaluated the impact of dry mouth with tolterodine 2 mg b.d. and oxybutynin 5 mg b.d. using a `Xerostomia Questionnaire.' The authors reported no significant differences between groups in this outcome, but no numerical results were presented.388 [EL 1 + ] Transdermal oxybutynin versus extended release tolterodine Transdermal oxybutynin 3.9 mg was compared with ER tolterodine 4 mg o.d. in a placebocontrolled DB RCT in men and women with frequency and urge UI n 361; 93% women ; . No significant differences were seen between active treatments in any outcome frequency, leakage episodes, QOL, adverse effects ; after 12 weeks' treatment. Improvements in frequency were significantly greater with tolterodine compared with placebo, and significantly greater benefit was seen in leakage episodes and subjective cure or improvement with both active drugs compared with placebo.351 [EL 1 + ] Immediate release oxybutynin versus extended release tolterodine Extended release tolterodine 4 mg o.d. was compared with IR oxybutynin 3 mg t.d.s. in a placebocontrolled DB RCT in men and women with urgency, frequency, and urge UI n 605; 70% women ; . No differences in efficacy measures were seen between tolterodine or oxybutynin, but fewer people treated with tolterodine experienced dry mouth after 12 weeks' treatment. Improvements in leakage episodes and frequency were significantly greater with active treatment compared with placebo. No significant differences were seen between the three groups in the proportion of people reporting improvement. Overall, 24% had received prior drug treatment for OAB; the response in these patients was not considered separately.352 [EL 1 + ] Treatment was continued in 31% of patients for up to 12 months; the results available indicate continued efficacy.395 [EL 3] Extended release oxybutynin versus immediate release tolterodine One DB RCT compared IR tolterodine 2 mg b.d. with ER oxybutynin 10 mg o.d. in men and women with urge UI, of whom 40% had previously been treated with antimuscarinic drugs n 378; 83% 69.
So, when you want to know more about cancer, call the Cancer Information Service 1-888-939-3333; Monday to Friday, 9 a.m. to 6 p.m. The Canadian Cancer Society's Information Service - Canada's only national, bilingual, toll-free service - offers comprehensive, credible information to cancer patients, their families, the public and healthcare professionals. Copied from: When You Want to Know More About Cancer and videx. Hydroxytolterodine is also the major metabolite of tolterodine nilvebrant et al, 1997, eur j pharmacol, 3 5-207!
When asthma treatment is taken consistently, most people can achieve good symptom control using lowdose inhaled corticosteroids and a bronchodilator as needed. Unfortunately, adherence to treatment can be compromised by concerns over safety, problems with inhaler technique and the difficulty of accepting the need to take medication even when you feel well. This unfortunately leads to asthma being less well controlled that it could be. People may say their asthma is well controlled, but when asked specific questions about symptoms, it's clear they have uncontrolled disease. Nevertheless, the number of people requiring hospitalization or dying from asthma has fallen significantly in recent years. Once COPD is established, it's difficult to reverse the changes. Despite the presence of a fixed airflow obstruction, it's clear that improved symptom control and a reduction in the frequency of exacerbations can be and digoxin and tolterodine, because medications. Department of biochemistry and molecular biology, school of medicine, university of louisville, louisville, kentucky 40292, usa angiotensin ii- and k + -stimulated aldosterone production in the adrenocortical glomerulosa cells requires induction of the steroidogenic acute regulatory protein star. Designated drug and Prescription drug Approval No. Date of listing in the NHI reimbursement price Date of initial marketing in Japan International birth date 8AM-77 Apr 1996 Apr 1996 Jan 1996 and dipyridamole. Prices of drugs produced by a manufacturer other than the originator of the brand drug are highlighted in bold. N A indicates that prices were not available at the time this report was written. * non-institutional prices.
Janet Meyers and Michel Pacqu from Child Survival Technical Support Plus CSTS + ; visited AMREF African Medical and Research Foundation ; in Kenya and CWI Concern Worldwide Incorporated ; in Bangladesh to identify solutions to problems and challenges to the implementation of the MAMAN package and to assess the possibility of measuring annual progress. The visit included working with PVO staff, local partners as well as other interested stakeholders. AMREF, Kenya was in the first year of the Child Survival and Health Grants Program CSHGP ; and CWI, Bangladesh was in its second year of implementation. During the visit practical problems and solutions to problems were identified and discussed. A description of findings during the visit is given below: AMREF, Kenya: CSHGP supported project of AMREF reconstructed the MAMAN package to make it applicable to the Kenyan setting and found that a separate work plan was not needed for implementing it. The project assigned specific roles for the district medical office, AMREF staff, communities and families to implement the package. After the initial implementation, a lot quality assurance sampling LQAS ; survey was conducted. Data from this survey were compared with baseline survey data of a subset of mothers having 0-11 month old children. After one year of implementation, improvement of TT coverage and maternal postpartum visits were observed. Proportions of babies received clean cord care, drying and wrapping, colostrums feeding, postnatal visit were 75, 44, 91 and 20 percent respectively. Fourteen percent mothers received AMTSL during their childbirths. However, these indicators were not included during baseline survey. No improvement was noticed in skilled attendance at delivery and immediate initiation of breastfeeding. Due to paucity of information, AMREF proposed to implement an operation research protocol to generate evidence of feasibility and effectiveness of MAMAN. CWI, Bangladesh: CWI, White Ribbon Alliance, and Child Survival Technical Support Plus CSTS + ; conducted a technical consultative meeting around the MAMAN package where the following key points emerged: About components of MAMAN package: The two postpartum visits suggested by MAMAN the first within 24h and the second between 3rd to 6th postpartum day ; should be conducted keeping in mind that cultural taboos may prevent some women leaving the home during the first 7 days after delivery of the baby. Answers to who would conduct these visits, where they would be conducted and what messages would be imparted, may be available from upcoming research from ICDDR, B.
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We then will ask you what your goal is, and if the side-effects of your medications are tolerable to get to that goal. Severe dry mouth Zinner et al., 2002 ; , and there is a 23% lower incidence of dry mouth reported with once-daily extendedrelease tolterodine capsules than with twice-daily immediaterelease tablets Clemett and Jarvis, 2001 ; . Propiverine hydrochloride, a safe and effective antimuscarinic drug as effective as oxybutynin, has a lower severity and incidence of dry mouth Noguchi et al., 1998; Madersbacher et al., 1999.

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Downloaded from archophthalmol on September 20, 2007 2003 American Medical Association. All rights reserved. 2.1 Ontology One key component of the Semantic Web technology involves the development and use of standard machine-readable ontologies to facilitate knowledge representation and semantic interoperability. Unlike data models, which are focused on typing and structural association of attributes, ontologies convey much more richly the semantics meanings ; of data. The Semantic Web uses ontologies to capture domain concepts, their relationships, and associated data: an ontology is "the specification of a conceptualization" of a knowledge domain [7]. The Semantic Web data integration approach [8] presents standard machinereadable ontologies ubiquitously on the web, in the form of triple-associations [9] or, more elegantly, of a description logic [10]. The ontologies are thereby exposed to processing by Web-aware agents, as well as to human access and interpretation. This facilitates extensible knowledge representation and semantic interoperability, and critically deepens our ability to treat the Web as a true knowledge base. An ontology consists of relatively generic knowledge that can be reused by different kinds of applications within a knowledge domain. In multi-domain investigations such as neuroscience, constructing mappings across the domains becomes a critical interoperability concern. One general approach to multi-domain data integration involves mapping between domain schemas or ontologies and a common cross-domain or "upper" schema or ontology. A significant number of ontologies have been developed in different biomedical domains including the neuroscience domain ; . They vary in size and expressiveness. The less expressive ontologies are called "weak ontologies" e.g., standard vocabularies and taxonomies ; and the more expressive ones are called "strong ontologies" e.g., thesauri ; . There is an increasing need for using expressive bio-ontologies to facilitate machine-based data integration and data mining. Recognizing this need, community efforts have begun to build ontologies for use by computer applications deployed in different domains of biosciences. Examples include the Gene Ontology [11] a controlled vocabulary describing gene and gene product attributes in any organism ; , Plant Ontology [12] a controlled vocabulary describing plant structures and growth and developmental stages ; , and Unified Medical Language System [13] which consists of a vocabulary database about biomedical and health related concepts ; . To provide a common access to these separately developed bio-ontologies, the Open Biomedical Ontologies [14] a centralized web resource for providing access to a variety of ontologies related to biomedical sciences ; has been created. Many of these bio-ontologies can be crossreferenced or inter-linked to facilitate more comprehensive knowledge acquisition and engineering. In addition to domain-specific ontologies, there is a desire to create an upper ontology that is limited to concepts that are meta, generic, abstract and philosophical, and therefore are general enough to address at a high level ; a broad range of domain areas. Concepts specific to given domains will not be included; however, this standard will provide a structure and a set of general concepts upon which domain-specific ontologies e.g. microarrays, proteomics, and pathways ; could be constructed. Examples of upper ontologies in the biological domain include Functional Genomics Investigation Ontology FuGO ; : fugo.sourceforge ; and EXPO.

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Figure 1. Adjusted mortality curves for patients hospitalized with heart failure and diabetes receiving prescription for thiazolidinedione TZD ; at hospital discharge and patients not treated with insulin-sensitizing drug. Knuth DE: Searching. In: Varga RS, Harrison MA, editors. The art of computer programming Volume 3: sorting and searching. Addison-Wesley, 1973: 391-2. 2. Greenfield RH. An experiment to measure the performance of phonetic key compression retrieval schemes. Methods Inf Med 1977; 16: 230-3. Feller WF. An introduction to probability theory and its applications. 3rd edition. Wiley, 1967; 1: 33 Fenna D: Phonetic reduction of names. Computer Programs in Biomedicine 1984; 19: 31-6. HB Newcombe Handbook of record linkage. Oxford: Oxford Medical Publications, 1988: 183-4. J Y Mortimer MA, J A Salathiel BSc PHLS AIDS Centre Communicable Disease Surveillance Centre 1.
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