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  1. Home
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  3. Amyotrophic Lateral Sclerosis
  • Cited by 23
Publisher:
Cambridge University Press
Online publication date:
March 2010
Print publication year:
1998
Online ISBN:
9780511663307
DOI:
https://doi.org/10.1017/CBO9780511663307
Subjects:
Neurology and Clinical Neuroscience, Medicine
Information

Book description

Amyotrophic lateral sclerosis (ALS), otherwise known as Lou Gehrig's or motor neuron disease, is one of several degenerative diseases of the ageing nervous system. Commonly affecting those in their mid-50s and beyond, it is a progressive illness resulting in death within a few years. This text neatly synthesizes the recent explosion of research into this particular condition to construct a detailed and comprehensive overview. From its epidemiology, molecular biology and pathophysiology right through to clinical assessment and care, Professor Eisen and Dr Krieger use their research expertise and extensive clinical experience to provide this practical and thought-provoking account.

Reviews

‘… this volumes strengths - its clarity, brevity, and breadth of vision - are to be applauded. Where else would one find tidy one-paragraph descriptions of the basis of magnetic resonance spectroscopy, or the difference between an odds ratio and a relative risk? I have already lent out my copy of this handy little one volume summation and recommend it as a launchpad for readers’ further investigations into ALS/MND.’

Matthew Parton Source: Journal of Neurology, Neurosurgery and Psychiatry

‘This excellent review of ASL is well-written in a language easily understood even by medical students and residents. Thus it appeals to health professionals involved in the care of patients with the disease and makes it different from other books written on this subject.’

Cristina Y. Go Source: Doody's Journal

‘The background of the authors ensures that issues relevant to neurologists interested in amyotrophic lateral sclerosis are discussed in a comprehensive and practical way. Readers will be impressed as well as educated by the data gathered from the author’s experience over a period of almost two decades.’

Source: The New England Journal of Medicine

‘The volume is amply illustrated and balanced in its approach. It is strongly recommended to all physicians, researchers and health care professionals involved in the management of ALS sufferers and their carers. It will also be a useful reference resource for medical libraries.’

Source: Neuromuscular Disorders

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