Table 2 Mean gastric emptying time in minutes ; and type of feed Pre intervention GET Test BM n 9 ; HMF n 5 ; Control BM n 19 ; HMF n 1 ; 76.44 86.31 76 Post intervention GET 71.33 78.92 74.48 p value 0.016 0.022 0.773.
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Newer agents for the acute treatment of migraine attacks have helped many migraine sufferers to maintain their productivity and quality of life. Efficacy and speed of onset vary by choice of medication and route of administration. Nasal spray formulations of triptans offer migraine sufferers a convenient, safe and rapid way to stop or lessen the effects of migraine, particularly when used early in an attack while pain is still mild. Moreover, nasal spray formulations offer prompt therapeutic intervention for patients with nausea and those in whom GI function may have been compromised by migraine.
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Abstract The terahertz region of the electromagnetic spectrum spans the frequency range between the mid-infrared and the millimeter microwave .For some imaging cases , using of viability terahertz signals is preferred to nuclear and x-ray imaging ee electron lasers , lamps , gas lasers and recently semiconductor electronic mixers and femtosecond laser are techniques to produce terahertz signals. Basic THz mixer elements are produced by standard semiconductor science and technology .Recent demonstrations, using pulsed near-infrared femtosecond laser systems, of the viability of THz medical imaging and spectroscopy have sparked international Interest ; yet much research still needs to be undertaken to optimize both the power and bandwidth in such THz systems . In this article, it is described imaging techniques, and commercial applications of T-ray imaging. T-ray computed tomography, Tray diffraction tomography, and tomographic imaging with a Fresnel binary lens are three Tray terahertz wave ; tomographic imaging modalities that are compared in this paper.
It was believed that the drug might reduce levels of an immune system chemical called tumor necrosis factor tnf and cloxacillin, for instance, dogs.
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Women saw themselves as hard workers, dedicated to the cause, and part of the team. They managed complex situations and often helped promote the health of their co-workers, both male and female, in their multiple roles. It is important that NPs understand the experiences of military women in order to provide sensitive and comprehensive health care. Promotion of women's health throughout the military will benefit all women. References.
The lack of any need for federal At the margin, malpractice abuse has surely steered some patients across state lines to find better intervention is eloquently proven health care, and it has surely influenced young phyby state med-mal reform being sicians' choice of specialties and of geographic locaubiquitous. More than three tions . But intrastate regulation of in-state conduct is dozen states have passed damage simply not interference with interstate commerce -- caps. All 50 states have either if I wrong on this count, then there is no area immune from federal jurisdiction, and we don't live in passed or are currently considera federal republic. Naturally, there's an effect on coming some kind of med-mal reform. merce when any individual or company withdraws from a state. But if a move from one state to another is the result of unfriendly in-state negligence claims, then as long as there is no discrimination against out-of-state parties, the effect is not uniquely related to the interstate aspect of commerce and cromolyn!
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The radioligand binding characteristics of `251-R ; 4-iodo2, 5dimethoxyphenylisopropylamine [Y-R ; DOI] and 3Hketanserin were compared in rat and bovine cortical membranes. In rat cortex, `251-R ; DOI labels a relatively low density of binding sites B , 2.5 & 0.2 pmol gm tissue ; with high affinity CD 0.63 & 0.09 nh! ; . In bovine cortex, specific binding of `a51-R ; DOI represents less than 20% of total binding at radioligand concentrations above 0.6 nM, and, therefore, the data cannot be analyzed adequately by Scatchard transformation. By contrast, 3H-ketanserin displays saturable, specific high-affinity binding in both rat cortex CD 1 .O -t 0.1 nM; B , 11 * 0.4 pmol gm tissue ; and bovine cortex KD 1.2 + 0.2 nu; B , 5.3 + 0.4 pmol gm tissue ; . K, values for 30 drugs were determined for 125l-R ; DOIlabeled sites in rat cortex and 3H-ketanserin-labeled sites in bovine cortex. L-Hydroxytryptamine 5-HT ; displays 250-fold higher selectivity for the 1251-R ; DOI-labeled sites Ki 3.0 ? 0.7 nM ; than for the 3H-ketanserin-labeled sites K, 750 ? 50 nM ; Structural congeners of R ; DOI display 80- to 160-fold higher affinity for the `V-R ; DOI binding site than for the 3H-ketanserin-labeled binding site. d-LSD and putative 5-HT, antagonists are approximately equipotent at both sites. Significant correlations were found between drug affinities for r251-R ; DOI-labeled sites in rat cortex and putative 5-HT sites labeled previously by "Br-R ; DOB r 0.93, p O.Ol ; , putative 5-HT sites labeled by 3H-ketanserin in bovine cortex r 0.63, p O.Ol ; , and 5-HT binding sites that have been characterized by other investigators r 0.78, p 0.01 ; . No significant correlations were found between drug affinities for 125l-R ; DOI-labeled sites in rat cortex and 5-HT , 5-HT , 5-HT , or 5-HT, sites, as determined by previous investigators. We conclude that Y-R ; DOI labels a novel 5-HT binding site subtype tentatively designated the 5HT binding site ; that is present in rat cortex but is either absent or minimally present in bovine cortex. By contrast, 3H-ketanserin labels both the putative 5-HT site in rat cortex as well as a separate, distinct recognition site that is present in both rat and bovine cortex, tentatively designated the 5-HT site.
But to my mind, pit-bull tactics are not legitimate in the critical debates about judicial funding and judicial management. Instead, I shall continue to work cooperatively and courteously with the executive and the legislative branches. There are no easy answers. No arm of government has a lock on the all the right responses to the question how best to deliver justice in our complex world. In shaping our judiciary to meet the needs of the 21st century, I do believe that involvement of the representatives of the private sector, community organizations, and public interest groups is crucial. Just as they have in decisions concerning Logan Airport and the reformation of statehouse administration, private citizens can help inform the discussion about advancing the judiciary's core missions. Recently I assembled a committee of some of the finest management and fiscal minds in the commonwealth into a Visiting Committee on Management in the Courts to assess the managerial practices and policies of the court system and make recommendations to improve the delivery of service in the administration of justice. Committee members, chaired by J. Donald Monan, S.J. Chancellor of Boston College, are prominent citizens who have been elected or appointed or promoted to positions at the highest levels. They have collective decades' worth of experience successfully running large institutions, both public and private, managing huge sums of money, both public and private, and planning for change and development. It was not easy to convince these individuals to donate their scarce time to assisting the courts, but they have. The members of the Visiting Committee will conduct interviews with members of the judicial branch and the citizens we serve, they will review documents and speak to experts, they will look at best practices elsewhere, and in six months they will report to the justices with concrete suggestions for reforming judicial administration. I eagerly await their findings. I have heard it said that justice is like oxygen. When it is flowing freely, no one notices. When the supply gets cut off, it may well be too late to notice. By focusing on the delivery of justice as well as on the ideal of justice, we can all take action to ensure that justice in the commonwealth of Massachusetts flows freely for many generations to come and ddavp.
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Option 1. YES. I want to receive these laboratory tests. I understand that Medicare will not decide whether to pay unless I receive these laboratory tests. Please submit my claim to Medicare. I understand that you may bill me for laboratory tests and that I may have to pay the bill while Medicare is making the decision. If Medicare does pay, you will refund to me any payments I made to you that are due to me. If Medicare denies payment, I agree to be personally and fully responsible for payment. That is, I will pay personally, either out of pocket or through any other insurance that I have. I understand I can appeal Medicare's decision. Option 2. NO. I have decided not to receive these laboratory tests. I will not receive these laboratory tests. I understand that you will not be able to submit a claim to Medicare and that I will not be able to appeal your opinion that Medicare won't pay. I will notify my doctor who ordered these laboratory tests that I did not receive them, for instance, clemastine fumarate syrup.
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Department of psychiatry and behavioral sciences, stanford university school of medicine, stanford, california 94305-5723, usa anticonvulsant drugs acs ; have diverse antiseizure, psychotropic, and biochemical effects and stimate.
15. Which one of the following is a relatively common change in antimicrobial pharmacokinetics in critically ill patients compared to noncritically ill patients? A. Increased volume of distribution. B. Increased absorption of oral and transdermal drugs. C. Decreased clearance because of hypermetabolic state. D. Increased protein binding. 16. Which one of the following empiric dosing adjustments should be considered in critically ill patients compared to data from healthy volunteers? A. B. C. Decrease the dose. Increase the dose. Increase dosing interval. Monitor free unbound ; serum concentrations, for instance, clemastine syrup.
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Bureaucratically challenged, especially by pharmacists and non-clinical personnel. Combine the formularies in the National Capitol Area. Patients should be able to visit the closest MTF and get refills or new prescriptions. Cut back on non-Prime prescriptions from non-MTF civilian ; providers. Electronic requests for non-formulary drugs. Removal of OTCs or OTCs available to patients without a prescription. Allow SPP medication requests to be filled at satellite clinics for the patient's convenience. DoD should have one formulary--most conversions are started due to [transfers] from one MTF to another. Make it easier to add medication to the formulary. 1 ; Standardize the process. 2 ; Different medications [should not] require different forms. 3 ; Pharmacy never gives the patient the form, so I have to try to find one. Clinic does not always have one. 4 ; Sometimes I'm not sure what form is needed. Need more coordination of formularies in the National Capitol Area Washington, D.C. ; between the Air Force, Army, and Navy. Particularly for consultants, it can be difficult to care for people if they can't get a drug refilled at their local MTF and have to get it at consultant's MTF only or [through a] civilian source. 1 ; Get rid of OTCs--patients waste valuable appointment slots for "refills" of OTCs. 2 ; DoD should allow for samples--it's the only way we can gain experience with new drugs. [There should be] electronic processing of "special drug requests." These requests [now] require the physician to hand-carry the form through the approval process or [else] it gets left on someone's desk indefinitely. Better, searchable drug database with classes of drugs and costs available [in the database]. Needs to be quick and easy to use. 1 ; Updated formulary. 2 ; Updated computer program for prescribing. Computerized formulary with drug class groups and desmopressin.
NOTICE IS HEREBY GIVEN to recipients, providers of services, and to the public of additions, effective February 19, 2003, to the state Medical Assistance maximum allowable cost MAC ; list for outpatient prescribed drugs. At least once each calendar year, the United States Department of Health and Human Services, Centers for Medicare & Medicaid Services, publishes a federal upper limit FUL ; payment schedule for many commonly prescribed multiple-source drugs. The FUL is set at a rate equal to 150 percent of the published price for the least costly therapeutic equivalent drug that can be purchased by pharmacists. This FUL payment schedule constitutes the federal MAC list. For many multiple source drugs that are not on the federal MAC list, the Department establishes a state MAC list. The Department requires Medical Assistance pharmacy providers to submit their usual and customary costs. Pharmacy providers are reimbursed at the lower of: the federal or state MAC, plus a dispensing fee; the submitted usual and customary charge to the general public; or a discount off of average wholesale price, plus a dispensing fee. On January 13, 2003 at 27 SR 1117-1130, the Department published notice of the MAC list, showing the federal and state MACs. Effective February 19, 2003, the following drugs will have a state MAC: MAC Generic Name ACETAZOLAMIDE 125MG TABLET 0.0761 ACETIC ACID HYDROCORTISONE 2-1% DROPS 1.6372 AMITRIPTYLINE HCL 25MG TABLET 0.082 AMOXAPINE 100MG TABLET 1.0207 AMOXAPINE 150MG TABLET 1.1172 AMPICILLIN TRIHYDRATE 250MG 5ML ORAL SUSP 0.0389 ANTIPYRINE BENZOCAINE GLYCERIN 5.4-1.4% DROPS 0.1048 BETAMETHASONE DIPROPIONATE 0.05% CREAM 0.1314 BETAMETHASONE DIPROPIONATE 0.05%OINT. ML ; 0.2146 BETAMETHASONE VALERATE 0.10% OINT. ML ; 0.0717 BISACODYL 10MG SUPP. RECT 0.1043 BUSPIRONE HCL 5MG TABLET 0.1373 CEPHRADINE 250MG CASULE 0.3653 CHLOROTHIAZIDE 250MG TABLET 0.0488 CHLOROTHIAZIDE 500MG TABLET 0.1205 CHLORPROMAZINE HCL 100MG TABLET 0.3786 CHLORPROMAZINE HCL 10MG TABLET 0.1627 CHLORPROMAZINE HCL 200MG TABLET 0.4446 CHLORPROMAZINE HCL 25MG TABLET 0.2519 CHLORPROMAZINE HCL 50MG TABLET 0.3182 CLEMASTINE FUMARATE 0.67MG 5ML SYRUP 0.0423 CLEMASTINE FUMARATE 2.68MG TABLET 0.3573 CLOTRIMAZOLE 1% CREAM 0.1354 CLOTRIMAZOLE 1% CREAM APPL 0.072 CLOTRIMAZOLE 1% SOLUTION 0.1168 CLOTRIMAZOLE BETAMET DIPROP 1-0.05% CREAM 0.9177 CODEINE PHOSPHATE ASPIRIN 30-325MG TABLET 0.0667 COLCHICINE 0.6MG TABLET 0.049 CORTISONE ACETATE 25MG TABLET 0.2927 CYCLOPENTOLATE HCL 1% DROPS 0.972 CYPROHEPTADINE HCL 4MG TABLET 0.2272 DANAZOL 200MG CASULE 2.8653.
Medication thiazide diuretic loop diuretic corticosteroid anti-ht heparin lmw heparin estrogen -blocker medications, mean sd ; , no and decadron.
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Ably similar. The midpoint of the h curves are 72 mV Table 8 ; . Native T-type currents inactivate over a similar range. These studies indicate that T-type channels, as observed with other channels, can reach inactivated states without passing through open states 364 ; . In fact, during a depolarizing pulse up to 30% of Cav3.3, channels inactivate without opening 127 ; . Cav3 channels recover rapidly from short-term inactivation. Cav3.1 channels recover fastest, displaying a monoexponential recovery with a time constant of 100 ms Fig. 7, Table 8 ; . In contrast, Cav3.3 channels recover threefold more slowly, while Cav3.2 channels recover.
The patient left the hospital against medical advice after being told that he could not smoke and dexamethasone and clemastine, for instance, fexofenadine.
Adverse effect of linezolid, and that close weekly monitoring is recommended in the following patients: those who receive 10-14 days therapy those with existing bone marrow suppression those who are receiving other drugs that may adversely affect haemoglobin levels, platelet function or blood counts those with renal insufficiency.
Accolate Accupril Accuretic Accutane * Accuzyme * acebutolol * Aceon acetazolamide * acetic acid-aluminum acetate * acetic acid ear drops * acetohexamide * acetylcysteine * Actifed-C * Actigall * Actinex Actiq PA ; Actos PA ; acyclovir * not ointment ; Adalat CC * Adderall * XR non-preferred ; Adrenalin Advair Advicor Agenerase Aggrenox Agrylin albuterol * albuterol ipratropium Aldactazide * Aldactone * Aldomet * Aldoril * Alesse * Alkeran Allegra, D allopurinol * Alocril Alomide Alphagan * alprazolam * Altoprev lowest copay ; aluminum chloride * Alupent * amantadine * Amaryl Amicar * amiloride * amiloride HCTZ * aminocaproic acid * amiodarone * amitriptyline * amoxapine * amoxicillin * amoxicillin-pot clavulanate * Amoxil * amphetamine * ampicillin * amylase-lipase-protease * Anafranil * Anakit Analpram HC Anaprox, DS * Anaspaz * Android * Ansaid * Antabuse * Anturane * Anusol-HC * Apresazide * Apresoline * Aralen * Arava Aricept Arimidex Aromasin Artane * Asacol Asendin * aspirin butalbital caffeine * aspirin caff butalbital codeine * Astelin Atarax * atenolol * atenolol chlorthalidone * Ativan * atropine * Atrovent soln. & inhaler * A T S * Augmentin * Augmentin ES Augmentin XR Auralgan * Avandamet PA ; Avandia PA ; Avelox Aventyl * Aygestin * Azathioprine * Azelex Azmacort Azopt Azulfidine * Betoptic * Betoptic S Biaxin, XL Bicitra * Biltricide bisoprolol HCTZ * Bleph-10 * Blephamide Blocadren * Brethine * Bromfed, PD, TD, DM * bromocriptine * bumetanide * Bumex * buproprion * Buspar * chlorthalidone * choline & magnesium salicylates * cholestyramine * Ciloxan cimetidine * Cin-Quin * Cipro * Ciprodex Claritin * See Generic: Loratadine ; Claritin-D 24 Hour * See loratadine D 24 Hour ; Claritin Syrup * See loratadine syrup ; Claritin Reditab Not Covered ; Claritin-D 12 Hour Not Covered ; Cleocin, Vag, T * clemastin 2.68mg * clidinium chlordiazepoxide * Climara * clindamycin * Clinoril * clobetasol ointment * clomipramine * clonazepam * clonidine * clorazepate * SD non-preferred ; clozapine * Clozaril * codeine * Cogentin * colchicine * Colestid Colyte * Combivent Combivir Compazine * Comtan Concerta Condylox Gel, Soln * Cordarone * Coreg Corgard * Cortef * Cortenema * Cortifoam Cortisporin * Cotazym Cotazym-S Coumadin * Cozaar Creon * Crixivan Crolom * cromolyn sodium * ophth ; Cuprimine cyclobenzaprine * Cyclogyl * cyclopentolate * cyclophosphamide * cyclosporine * Cycrin * Cylert * cyproheptadine * Cystospaz * Cytadren Cytomel * Cytotec * Cytovene Cytoxan and divalproex!
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2. Responses of Placebo Group During Medication and Postmedication Periods.
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Selective 5 -HT reuptake inhibitors SSRIs ; Serotonin Hypothesis of Depression 5-HT is a major player in depressive illness and serotonergic pathways are closely related to mood disorders, especially depression Fig. 45.1 ; 51 ; . Thus drugs affecting the 5-HT levels in the neural synapse and serotonergic pathways may lead to effective therapy of depression. 5-HT is synthesized from tryptophan, packaged into vesicles, and released into the synaptic cleft following an action potential Chapter 12 ; . Once in the synaptic cleft, 5-HT interacts with both the pre- and postsynaptic serotonergic receptors. Evidence implicating multiple abnormalities in serotonergic pathways as a cause of depression include: 1 ; low urinary concentrations of 5-HT's major metabolite, 5hydroxyindoleacetic acid; 2 ; a low density of brain and platelet 5-HT transporters in depressed individuals; 3 ; a high density of brain and platelet 5-HT binding sites; and 4 ; a low synaptic concentration of tryptophan which is used in 5-HT synthesis. Of these, the low level of 5-HT transport proteins SERT ; in depressed patients has received the most attention in the development and synthesis of the SSRIs. While the precise antidepressant mechanism of action for the SSRIs eludes neuroscientists, SSRIs have been shown to alleviate depression and are the most common drugs used in the therapy for depression. Claims of decreased adverse effects ADRs ; , less toxicity in overdose than both the MAOIs and the TCAs, and increased safety have led to their extensive use and several are ranked in the top 50 prescription drugs dispensed in 2002. The SSRIs are proven treatments for depression, OCD, and panic disorder and have been found to be helpful in a variety of other conditions, as well. The most substantial benefit for the SSRIs is their adverse effect profile which differs from the TCAs and are slightly better tolerated. Although the SSRIs have become the most commonly prescribed drugs for depression, there are clinical situations in which TCAs may be more appropriate, e.g., melancholic depression. Meaningful differences between the SSRIs is largely related to their pharmacokinetics, metabolism to active metabolites, inhibition of CYP450 isoforms and effect of drugdrug interactions, and the half-life of the SSRI. The SSRIs are expensive, and it has been common to have non-compliant patients especially elderly ; relapse because they can not afford their medications. Persuading the patient to take his or her medication as prescribed is extremely important in potentially suicidal patients with depression. Because of this, it is exceedingly important that patients receive the lowest effective and thereby the most cost effective ; dose of any drug they are prescribed. Structure -Activity Relationships Comm on to the SSRIs Although the TCAs as a group ; are effective antidepressants, their adverse event profile and narrow and clopidogrel.
From Table 9, ARV drug costs account for the largest proportion of the total ART costs in both countries. Using costs relating to ARVs, Laboratory monitoring tests and service utilization by patients, the average ART costs per patient and proportions on SL regimens are given in Table 10 Table 10: Average ART costs US $ ; by year.
Celebrating Mother and Child on the Fortieth Day: The Sfax Tunisia Postpartum Program English only ; , no. 1, 1989. Man Hombre Homme: Meeting Male Reproductive Health Care Needs in Latin America English, Spanish ; , no. 2, 1990. Gente Joven Young People: A Dialogue on Sexuality with Adolescents in Mexico English, Spanish ; , no. 5, 1993. The Coletivo: A Feminist Sexuality and Health Collective in Brazil English, Portuguese ; , no. 6, 1995. Doing More with Less: The Marie Stopes Clinics of Sierra Leone English only ; , no. 7, 1995. Introducing Sexuality within Family Planning: Three Positive Experiences from Latin America and the Caribbean English, Spanish ; , no. 8, 1997. Using COPE to Improve Quality of Care: The Experience of the Family Planning Association of Kenya English, Spanish ; , no. 9, 1998. Alone You Are Nobody, Together We Float: The Manuela Ramos Movement English, Spanish ; , no. 10, 2000.
Treatments overview 1 overview of treatment options the available treatments for brain tumors can be broadly categorized as either conventional medicine or complementary alternative medicine cam.
Sources Carroll D, Finn C, Gill S, & Sawyer J. 2002 ; . A Comparison of Measurements from a Temporal Artery Thermometer and a Pulmonary Artery Catheter Thermistor. Poster presentation. : pcs.mgh.harvard CCPD Nursing Research Research Abstracts 2002 Greenes, DS & Fleisher, GR. 2201 ; . Accuracy of a Noninvasive Temporal Artery Thermometer. Archives of Pediatric & Adolescent Medicine 155: 376-381. Hockenberry, M.J. 2003 ; . Wong's Nursing Care of Infants and Children. 7th ed. ; . St. Louis: Mosby, pp.178183. Potter, P.A., & Perry, A. G. 2001 ; . Fundamentals of Nursing. 5th ed. ; . St. Louis: Mosby, pp.678-687.
Obligatory Must not donate if: a ; The condition for which treatment was given is not acceptable. b ; Less than 12 months from completing treatment. Discretionary 1. Performed within the NHS If performed by a suitably qualified NHS healthcare professional on NHS premises, accept. 2. Performed outside of the NHS a ; If performed by a Medical Practitioner registered with the General Medical Council GMC ; , accept. b ; If performed by a Nurse registered with the Nursing and Midwifery Council NMC ; , accept. c ; If a valid certificate is available from an acupuncturist registered with the Acupuncture Association of Chartered Physiotherapists or the British Acupuncture Council or the General Chiropractic Council or the General Osteopathic Council, accept, because clemastinf drug.
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June 2001 September 2001 Cullen N, Bayley M. Evaluation of Outcome of Slowstream Rehabilitation for Individuals with Extremely Severe Brain Injury Scholarships and Awards 1998 - 1999 R. Samuel McLaughlin Foundation Fellowship Award - $45, 000 for a one year fellowship in Traumatic Brain Injury at the Rehabilitation Institute of Michigan and Wayne State University. Emphasis on neuropharmacology in the brain injured. 1998 - 1999 - Rehabilitation Institute of Toronto - Research Foundation - $30, 000 Research scholarship for one year clinical research fellowship in Detroit, Michigan. Research Presentations Megan Mahabir, BSc, Nora Cullen, MD, Farooq Ismail, MD, Mark Bayley, MDThe Potential Benefits of Treating TBI Patients According to Functional Ability, CAPM&R, Edmonton, Alberta, June 13, 2003 Megan Mahabir, BSc, Nora Cullen, MD, Farooq Ismail, MD, Mark Bayley, MDThe Potential Benefits of Treating TBI Patients According to Functional Ability, GTA Network Conference, Toronto, Ont, Feb, 2003 Rajput A, Cullen N, Bayley M. Evaluation of Outcome of Slowstream Rehabilitation for Individuals with Extremely Severe Brain Injury, ABI Network Conference, Toronto November 2002 Agarwal V, Bayley M, Green R, Masanic C, Cullen N. Validity Testing of Neurological Soft Signs in an Acquired Brain Injury Population. Ontario Academic Physiatry Day, Toronto, September 2001. Cayen B, Cullen N, Bayley M. Dose-Response Relationship between Outpatient Rehabilitation and Outcomes in Traumatic Brain Injury Patients Ontario Academic Physiatry Day, Toronto, September 2001. Functional Outcomes of Patients with TBI after In-patient Rehabilitation: How Do We Compare? GTA Rehab Network Research Day, Feb, 2001, Toronto, Ont. Functional Outcomes of Patients with TBI after In-patient Rehabilitation: How Do We Compare? Seventh annual Academic Day for Ontario Physiatrists, Sept, 2000, Toronto, Ont. Reliability and Validity of Outcome Measures Used in Medical Rehabilitation Research Seventh annual Academic Day for Ontario Physiatrists, Sept, 2000, Toronto, Ont. Severe penetrating head injury : a preliminary look at outcome Third World Congress on Brain Injury, Quebec City, June, 1999.
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