Download Amyotrophic Lateral Sclerosis - A Bibliography and by Philip M. Parker PDF

By Philip M. Parker

ISBN-10: 0497113279

ISBN-13: 9780497113278

ISBN-10: 142949610X

ISBN-13: 9781429496100

In March 2001, the nationwide Institutes of future health issued the next caution: ''The variety of websites providing health-related assets grows each day. Many websites supply precious details, whereas others could have info that's unreliable or misleading.'' additionally, end result of the speedy bring up in Internet-based info, many hours could be wasted looking, deciding on, and printing. due to the fact purely the smallest fraction of data facing Amyotrophic lateral sclerosis is listed in se's, corresponding to www.google.com or others, a non-systematic method of web examine could be not just time eating, but additionally incomplete. This ebook was once created for doctors, scholars, and individuals of most of the people who are looking to behavior scientific study utilizing the main complex instruments on hand and spending the smallest amount of time doing so.

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Extra resources for Amyotrophic Lateral Sclerosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Or 2000 mg. daily). Stage 2 compares the selected dose against placebo to assess whether evidence of efficacy is sufficient to justify proceeding to a future phase III trial. The primary outcome measure is the change in ALS Functional Rating Scale revised (ALSFRSr) score from baseline (randomization) to 9 months. We chose the ALSFRSr because: (1) It measures daily living functional abilities, a clinically meaningful outcome; (2) it is a validated predictor of survival; and (3) its ease of administration will minimize subject dropout.

Another major area of study is to identify the nature and possible disorder of articulatory coordination in dysarthria. Dysarthria is often described as having a prominent component of articulatory dyscoordination, but the small amount of relevant data that exist have not revealed the kind of frank coordination disorder that might be expected from typical textbook descriptions. A finding from the first funding cycle of small abnormalities in the degree of coordination, but an essentially-normal 'form' of coordination for a particular phonetic sequence will be followed up with analyses of additional sequences, as well as with the inclusion of analyses of articulatory scale in these patients and in neurologically-healthy controls.

Aim 2 will determine whether CoQ 10 affects secondary measures: (1) forced vital capacity, (2) fatigue severity, (3) health-related quality-of-life, and (4) serum oxidative stress markers. Because median disease duration is short, the pool of ALS clinical trial participants at any given time is quite limited. Survival as an outcome measure is the gold standard for phase HI trials, but requires a large sample size. Because several new agents will soon be available for clinical testing, it is vital to reduce the number of patients required for phase II trials if these agents are to be tested in a timely, effective way.

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Amyotrophic Lateral Sclerosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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