Neuropathology Of Amyotrophic Lateral Sclerosis And Parkinsonism Dementia Complex On Guam PDF Download

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Bibliography of Amyotrophic Lateral Sclerosis and Parkinsonism-dementia of Guam

Bibliography of Amyotrophic Lateral Sclerosis and Parkinsonism-dementia of Guam
Author: Ralph M. Garruto
Publisher:
Total Pages: 190
Release: 1983
Genre: Amyotrophic lateral sclerosis
ISBN:

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Approximately 600 entries to literature (mostly journal articles) about Guam, the Kii Peninsula of Japan, and West New Guinea. Also includes as a supplement of additional selected references on history and geography, natural environment, general anthropology, and health and disease in Guam and the Northern Mariana Islands. Chronological arrangement of the main section. Each entry gives bibliographical information. Author index.


Spectrums of Amyotrophic Lateral Sclerosis

Spectrums of Amyotrophic Lateral Sclerosis
Author: Christopher A. Shaw
Publisher: John Wiley & Sons
Total Pages: 240
Release: 2021-04-20
Genre: Medical
ISBN: 1119745500

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SPECTRUMS OF AMYOTROPHIC LATERAL SCLEROSIS Discover state-of-the-art research findings on ALS from leading authors and editors in the field In Spectrums of Amyotrophic Lateral Sclerosis: Heterogeneity, Pathogenesis & Therapeutic Directions, distinguished researchers and editors Dr. Christopher A. Shaw and Jessica R. Morrice deliver a practical and powerful perspective on Amyotrophic Lateral Sclerosis (ALS) as a heterogeneous spectrum of disorders. This increasingly accepted point-of-view allows researchers and medical professionals to develop better targeted interventions and more precise therapies. In the book, readers will find chapters on a wide variety of critical issues facing ALS researchers and healthcare practitioners treating ALS sufferers, including animal models of ALS, neuronal support cells known to have a pivotal role in ALS, and current challenges in ALS clinical trials, among others. The authors describe pathologic features common to all cases of ALS and why animal models, though crucial, should be interpreted with caution. Finally, multiple genetic and environmental etiologies of the disease are discussed. Readers will also benefit from the inclusion of: A thorough introduction to ALS as a spectrum disease and the implications for models, therapeutic development and clinical trial design Explorations of the genetic basis of ALS, prospective sALS etiologies, and the involvement of microbiome in ALS Discussions of ALS-PDC and environmental risk factors, protein aggregation in ALS, defects in RNA metabolism in ALS, and the non-cell autonomous nature of ALS and the involvement of glial cells Examinations of animal models of ALS and perspectives on previously failed ALS therapeutics and current therapeutic strategies Perfect for clinical neurologists, healthcare providers and caretakers, clinicians, and researchers studying motor neuron disease, Spectrums of Amyotrophic Lateral Sclerosis: Heterogeneity, Pathogenesis & Therapeutic Directions is also an indispensable resource for the neurodegenerative research community, neurology residents, and graduate-level neuroscience students.


Amyotrophic Lateral Sclerosis and Parkinsonism-dementia Complex of Guam

Amyotrophic Lateral Sclerosis and Parkinsonism-dementia Complex of Guam
Author: Stephen Clay Waring
Publisher:
Total Pages: 338
Release: 1994
Genre: Amyotrophic lateral sclerosis
ISBN:

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The patterns of occurrence for both ALS and PDC overlap in most respects: (1) incidence and mortality are decreasing; (2) median age at onset is increasing; (3) males are at increased risk for developing disease; (4) risk is higher for those residing in the south compared to the non-south; and (5) age-specific incidence is decreasing over time except in the oldest age groups.


NIH Publication

NIH Publication
Author:
Publisher:
Total Pages: 192
Release: 1983
Genre:
ISBN:

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Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias

Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias
Author: Michael J. Strong
Publisher: Oxford University Press
Total Pages: 426
Release: 2012-10-11
Genre: Medical
ISBN: 0199590672

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This book summarizes the advances in our understanding of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), as well as the potential relationship between the two.


Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias

Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias
Author: Michael J. Strong
Publisher: OUP Oxford
Total Pages: 426
Release: 2012-10-11
Genre: Medical
ISBN: 0191637289

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Over the past ten years, there has been an increasing recognition that syndromes of frontotemporal dysfunction (FTD) are a common occurrence in patients with amyotrophic lateral sclerosis (ALS). Such syndromes may be present in as many as 60% of patients with ALS. Conversely, the occurrence of motor neuron dysfunction in patients with clinically pure frontotemporal dementia is increasingly recognized. This suggests that to some extent there are overlapping syndromes in which both ALS and FTD occur within the same individual. This volume summarizes the advances in our understanding of these two disorders, as well as the potential relationship between the two. Key topics include advances in our ability to clinically describe the frontotemporal syndromes, preclinical detection, neuroimaging, and genetics. The exploding field of new markers in neuropathology is examined, as is the role of new genetic mutations in DNA/RNA transport systems. This book is the essential reference text for this topic, and will be of interest to neurologists and neurological trainees with a clinical or research interest in the FTDs or ALS, neuropsychologists, neuropathologists, and researchers.


Neurodegeneration

Neurodegeneration
Author: Dennis Dickson
Publisher: John Wiley & Sons
Total Pages: 497
Release: 2011-09-09
Genre: Medical
ISBN: 1444341235

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Most textbooks on neurodegenerative disorders have used a classification scheme based upon either clinical syndromes or anatomical distribution of the pathology. In contrast, this book looks to the future and uses a classification based upon molecular mechanisms, rather than clinical or anatomical boundaries. Major advances in molecular genetics and the application of biochemical and immunocytochemical techniques to neurodegenerative disorders have generated this new approach. Throughout most of the current volume, diseases are clustered according to the proteins that accumulate within cells (e.g. tau, α-synuclein and TDP-43) and in the extracellular compartments (e.g. β-amyloid and prion proteins) or according to a shared pathogenetic mechanism, such as trinucleotide repeats, that are a feature of specific genetic disorders. Chapters throughout the book conform to a standard lay-out for ease of access by the reader and are written by a panel of International Experts Since the first edition of this book, major advances have been made in the discovery of common molecular mechanisms between many neurodegenerative diseases most notably in the frontotemporal lobar degenerations (FTLD) and motor neuron disease or amyotrophic lateral sclerosis. This book will be essential reading for clinicians, neuropathologists and basic neuroscientists who require the firm up-to-date knowledge of mechanisms, diagnostic pathology and genetics of Neurodegenerative diseases that is required for progress in therapy and management.


Bibliography of Amyotrophic Lateral Sclerosis and Parkinsonism-dementia of Guam

Bibliography of Amyotrophic Lateral Sclerosis and Parkinsonism-dementia of Guam
Author: Ralph M. Garruto
Publisher:
Total Pages: 0
Release: 1983
Genre: Amyotrophic lateral sclerosis
ISBN:

Download Bibliography of Amyotrophic Lateral Sclerosis and Parkinsonism-dementia of Guam Book in PDF, ePub and Kindle

Approximately 600 entries to literature (mostly journal articles) about Guam, the Kii Peninsula of Japan, and West New Guinea. Also includes as a supplement of additional selected references on history and geography, natural environment, general anthropology, and health and disease in Guam and the Northern Mariana Islands. Chronological arrangement of the main section. Each entry gives bibliographical information. Author index.