Amyotrophic lateral sclerosis or motor neurone disease is one of the most debilitating and devastating of the neurological diseases. The only comprehensive textbook available on the topic, this completely reorganized and expanded new edition examines all aspects of ALS from pathology to patient care and provides the reader with a ready reference to help with the difficulties encountered in patient diagnosis and treatment. Undoubtedly an important work in the field, this book will be of great interest to clinical neurologists and trainees, and to all those concerned with the care of people with ALS.
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Book Description
Editorial Reviews
From The New England Journal of Medicine
Amyotrophic lateral sclerosis is a progressive, paralyzing illness that is invariably fatal. It has been neglected until recently because there was only a poor understanding of pathogenesis and no treatment. Physicians often experience a sense of helplessness and frustration in conveying the diagnosis truthfully to patients and in helping them to cope with advancing disability and the prospect of death.
This book is an excellent review of amyotrophic lateral sclerosis with respect to clinical features, pathological findings, functional and physiologic studies, pathogenesis, therapeutic approaches, and patient care. It is an international effort, with its three editors from the United States, France, and the United Kingdom and 57 other contributors, all of whom are acknowledged experts in the field. It is a credit to the editors that the various chapters read seamlessly, with little sign of the multiple authorship. In addition, this is a handsome book with an excellent typeface.
All of the issues surrounding amyotrophic lateral sclerosis are dealt with in depth; a thought-provoking chapter covers the controversial subjects of physician-assisted suicide and euthanasia. I strongly recommend this compendium to neurologists and other physicians who provide care for patients with this illness.
Austin J. Sumner, M.D.
Copyright © 2000 Massachusetts Medical Society. All rights reserved. The New England Journal of Medicine is a registered trademark of the MMS.
--This text refers to an alternate
Hardcover
edition.
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First Sentence:
The nomenclature of disorders of the motor system can be confusing (Table 1.1). Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
motor neuron cell death, motor neurone injury, bulbar score, sporadic amyotrophie lateral sclerosis, post symptom onset, argument from double effect, diminished penetrance, neuron disease spinal cord, arm megascore, inclusion dementia, drop from baseline, familial amyotrophie lateral sclerosis, unit number estimates, extremity assistive devices, familial motor neuron disease, lateral sclerosis functional rating scale, motor neuron destruction, human motor neuron disease, human motor neurones, neuron cell line, amyotrophic lateral sclerosis mortality, conglomerate inclusions, juvenile muscular atrophy, juvenile amyotrophic lateral sclerosis, dismutase gene mutations Key Phrases - Capitalized Phrases (CAPs): (learn more)
Ann Neurol, Neurol Sci, Neurol Neurosurg Psychiatry, Proc Natl Acad Sci, Arch Neurol, Muscle Nerve, New York, Brain Res, Neurosci Lett, Acta Neurol Scand, Acta Neuropathol, Ben Hamida, Neuropathol Exp Neurol, Cell Biol, Hum Mol Genet, Gouri Devi, Rev Neurol, Electroencephalogr Clin Neurophysiol, Neuropatbol Exp Neurol, Adv Neurol, Hum Genet, Nat Genet, Acta Neuropatbol, Comp Neurol, Neurol Clin New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
The nomenclature of disorders of the motor system can be confusing (Table 1.1). Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
motor neuron cell death, motor neurone injury, bulbar score, sporadic amyotrophie lateral sclerosis, post symptom onset, argument from double effect, diminished penetrance, neuron disease spinal cord, arm megascore, inclusion dementia, drop from baseline, familial amyotrophie lateral sclerosis, unit number estimates, extremity assistive devices, familial motor neuron disease, lateral sclerosis functional rating scale, motor neuron destruction, human motor neuron disease, human motor neurones, neuron cell line, amyotrophic lateral sclerosis mortality, conglomerate inclusions, juvenile muscular atrophy, juvenile amyotrophic lateral sclerosis, dismutase gene mutations Key Phrases - Capitalized Phrases (CAPs): (learn more)
Ann Neurol, Neurol Sci, Neurol Neurosurg Psychiatry, Proc Natl Acad Sci, Arch Neurol, Muscle Nerve, New York, Brain Res, Neurosci Lett, Acta Neurol Scand, Acta Neuropathol, Ben Hamida, Neuropathol Exp Neurol, Cell Biol, Hum Mol Genet, Gouri Devi, Rev Neurol, Electroencephalogr Clin Neurophysiol, Neuropatbol Exp Neurol, Adv Neurol, Hum Genet, Nat Genet, Acta Neuropatbol, Comp Neurol, Neurol Clin New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
This book cites 44
books:
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35
books
cite this book:
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- Amyotrophic Lateral Sclerosis, Second Edition by Robert H. Brown Jr. on 9 pages
- Amyotrophic Lateral Sclerosis (American Academy of Neurology) by M.D. Robert G. Miller on 6 pages
- Amyotrophic Lateral Sclerosis by Imaharu Nakano on 4 pages
- Human Motor Neuron Diseases (Advances in neurology) by ROWLAND on 4 pages
- Motor Neuron Disease: Biology and Management by P. N. Leigh on page 71, page 72, and page 349
See all 44 books this book cites
- Neurodegenerative Diseases (Rhone-Poulenc Rorer Round Table Conferences) by G. Jolles on page 223, page 234, and page 235
- Brain Damage and Repair: From Molecular Research to Clinical Therapy by T. Herdegen on page 587, and page 599
- Pick's Disease and Pick Complex by Andrew Kertesz on page 159, and page 166
- Neurodegenerative Diseases (Gwumc Department of Biochemistry and Molecular Biology Annual Spring Symposia) by Gary Fiskum on page 130, and page 279
- Harrison's Manual of Medicine by Eugene Braunwald on page 877
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