Handbook of amyotrophic lateral sclerosis



Publisher: Dekker in New York

Written in English
Cover of: Handbook of amyotrophic lateral sclerosis |
Published: Pages: 783 Downloads: 992
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Subjects:

  • Amyotrophic lateral sclerosis.,
  • Amyotrophic Lateral Sclerosis.

Edition Notes

Includes bibliographical references and index.

Statementedited by Richard Alan Smith.
SeriesNeurological disease and therapy ;, v. 12
ContributionsSmith, Richard Alan, 1941-
Classifications
LC ClassificationsRC406.A24 H35 1992
The Physical Object
Paginationxxvii, 783 p. :
Number of Pages783
ID Numbers
Open LibraryOL1703291M
ISBN 100824786106
LC Control Number92004386

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  Amyotrophic Lateral Sclerosis. ALS, sometimes referred to as Lou Gehrig’s disease, involves the degeneration of motor neurons in the spinal cord. These neurons normally transmit signals and impulses from the brain to the rest of the body, but as the condition progresses the neurons harden and eventually die. Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterised by progressive muscular paralysis reflecting degeneration of motor neurones in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Incidence (average per ,/year) and prevalence (average per,) are relatively uniform in Western countries, although foci of higher frequency. Amyotrophic Lateral Sclerosis (ALS) can be inherited in an autosomal dominant (in about 10% of cases), autosomal recessive, or X-linked fashion. The remaining cases are believed to be either environmental (eg, manganese, mercury, fertilizers, insecticides, herbicides) or caused by . This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. This is a list of notable people who have or had amyotrophic lateral sclerosis (ALS). Astrophysicist Stephen Hawking, whose ALS was diagnosed in , had ALS for Events: ALS Awareness Month, Ice Bucket .

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a rapidly progressing disease that attacks the nerve cells in the brain that are responsible for controlling voluntary muscles. It is part of a group of diseases known as motor neuron disease, which is characterized by the degeneration and death of motor neuron cells.

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Handbook of Amyotrophic Lateral Sclerosis (Neurological Disease and Therapy) 1st Edition. by Richard Smith (Author) ISBN ISBN Why is ISBN important.

ISBN. This bar-code number lets you verify that you're getting exactly the right version or edition of a book. Cited by: Handbook. Amyotrophic Lateral Sclerosis Team Physician.

The ALS team physician is responsible for: (1) Starting the consultation by asking what the patient already knows or suspects. (2) Giving the diagnosis to the patient and discussing its implications in a stepwise fashion.

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Search in this handbook. Looking for an author or a specific volume/issue. Brain-computer interfaces for people with amyotrophic lateral sclerosis.

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Handbook of amyotrophic lateral sclerosis book Navigating Life with Amyotrophic Lateral Sclerosis provides accessible, comprehensive, and up-to-date information about the challenges patients, family members, and caregivers face when confronted by ALS, a disease Handbook of amyotrophic lateral sclerosis book affects approximately 5, Americans every year, with as many as 30, people managing the disease at any given time.

ALS is a difficult disease for the patient and is also /5(13). Amyotrophic Lateral Sclerosis summarises this new information. The editors are experts in the subject, and they have assembled an international collection of authors—59 of them, from 11 countries in four continents.

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(Monday through Friday am to pm PST). DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis – a randomised controlled trial. McDermott CJ, Bradburn MJ, Maguire C, et al. Southampton (UK): NIHR Journals Library; Jun. (Health Technology Assessment, No.

Amyotrophic lateral sclerosis (ALS) is a type of motor neuron disorder that rapidly and progressively attacks the nerve cells responsible for controlling voluntary muscles. We establish ALS under when you have a documented diagnosis of ALS. We require documentation based on generally accepted methods consistent with the prevailing state.

MDA is the world leader in fighting ALS (amyotrophic lateral sclerosis). If you’ve recently received an ALS diagnosis, this booklet will help you understand the disorder, while guiding you to the many services MDA provides.

MDA’s involvement with ALS began in the early s, when Eleanor Gehrig, widow of Yankees first basemanFile Size: 1MB. Amyotrophic lateral sclerosis is characterised by the progressive loss of motor neurons in the brain and spinal cord. This neurodegenerative syndrome shares pathobiological features with.

Handbook of the Aging Brain brings together diverse scientific disciplines to cover the most recent research findings in an easy-to-read summary. Scientists and clinicians will find a wide spectrum of subjects including gerontology, neurology, psychology, molecular biology, and cellular biology.

The word “amyotrophic” comes from Greek roots that mean “without nourish­ ment to muscles” and refers to the loss of signals nerve cells normally send to mus­ cle cells. “Lateral” means “to the side” and refers to the location of the damage in the spinal cord.

“Sclerosis” means “hard­. Book Review from The New England Journal of Medicine — Book Review Handbook of Amyotrophic Lateral Sclerosis.

This article has no abstract; the first words appear below. Amyotrophic Lateral Sclerosis: A Patient Care Guide for Clinicians is a practical reference for clinicians caring for ALS patients that brings together the collective wisdom of those at the forefront of patient-oriented research and practice.

The book compiles recent findings of both evidence-based and experience-based research to provide clinicians with tools that improve quality and length /5(8). Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease involving several protein mutations in glycine-rich regions with limited treatment options.

% of all cases are non. Amyotrophic Lateral Sclerosis: A Patient Care Guide for Clinicians is a practical reference for clinicians caring for ALS patients that brings together the collective wisdom of those at the forefront of patient-oriented research and practice.

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Reviews “Well written, easy to read, and highly educational, this book is a very nice addition to a neurologist's professional library.”. Amyotrophic Lateral Sclerosis - CRC Press Book Amyotrophic Lateral Sclerosis 1st Edition.

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Caplan, M.D. Professor of Neurology Harvard University School of Medicine Beth Israel Deaconess Medical Center Boston, Massachusetts, U.S.A. [Book] Handbook of Clinical Neurology - Chapter 13 - The epidemiology of amyotrophic lateral sclerosis. VHA HANDBOOK (1) Transmittal Sheet Ma VHA AUDIOLOGY AND SPEECH-LANGUAGE PATHOLOGY SERVICES 1.

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Information on pharmacologic treatment, both traditional and alternative, and noninvasive respiratory support has been updated from the publication/5(7). Amyotrophic lateral sclerosis (ALS), also referred to as "Lou Gehrig's disease," is a progressive motor neuron disease which leads to problems with muscle control and movement.

There are various types of ALS that are distinguished by symptoms and, in some cases, genetic cause. Early symptoms may include muscle twitching, cramping, stiffness, or weakness, slurred speech, and/or. Professor. Department of Clinical Medicine, University of Bergen and Department of Neurology, Haukeland University Hospital, Bergen, Norway.

Search for more papers by this authorCited by: 3. The name Amyotrophic Lateral Sclerosis (ALS) is derived from Greek: Amyotrophic meaning no muscle nourishment,’ Lateral refers to the lateral area.

4 in the spinal cord where the corticospinal fibers travel, and Sclerosis best describes the scarring thatFile Size: KB. Amyotrophic Lateral Sclerosis: A Patient Care Guide for Clinicians is a practical reference for clinicians caring for ALS patients that brings together the collective wisdom of those at the forefront of patient-oriented research and practice.

The book compiles recent findings of both evidence-based and experience-based research to provide clinicians with tools that improve quality and length.

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Conditions are presented in alphabetical order with extensive cross 5/5(3). Amyotrophic lateral sclerosis (ALS) is a rapidly progressive, fatal disease that affects the nerve cells (neurons) in that brain and spinal cord that control voluntary muscle movement.

Our voluntary muscles produce movements like walking, breathing, chewing, and talking. Nerve cells called motor neurons--that connect from the brain and spinal. See Amyotrophic Lateral Sclerosis (also known as Lou Gehrig’s disease) Ambulance servi 57 Ambulatory surgical center 36 Amyotrophic Lateral Sclerosis (ALS) 19 App –, Artiicial limbs 53 Assignm 64, B Balance exam 46 Barium enema .Amyotrophic lateral sclerosis (ALS), ∗ commonly known as Lou Gehrig's disease, is the most common and devastatingly fatal MND among adults.

ALS is characterized by the degeneration and loss of motor neurons in the spinal cord, brainstem, and brain, resulting .Amyotrophic Lateral Sclerosis: A Guide For Patients and Families, 3rd Edition This extensively revised and rewritten new edition of the bestselling Amyotrophic Lateral Sclerosis: A Guide For Patients and Families addresses all of those needs, and brings up-to-date .