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Neurodegenerative Diseases

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Cover of 'Neurodegenerative Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 Alzheimer’s Disease: Insights from Genetic Mouse Models and Current Advances in Human IPSC-Derived Neurons
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    Chapter 2 Clinical Aspects of Alzheimer’s Disease
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    Chapter 3 Parkinson’s Disease: Basic Pathomechanisms and a Clinical Overview
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    Chapter 4 Huntington’s Disease: Pathogenic Mechanisms and Therapeutic Targets
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    Chapter 5 The Complexity of Clinical Huntington’s Disease: Developments in Molecular Genetics, Neuropathology and Neuroimaging Biomarkers
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    Chapter 6 Motoneuron Disease: Basic Science
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    Chapter 7 Motoneuron Disease: Clinical
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    Chapter 8 Multiple Sclerosis: Basic and Clinical
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    Chapter 9 Schizophrenia: Basic and Clinical
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    Chapter 10 Stroke: Basic and Clinical
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    Chapter 11 Epileptic Encephalopathies as Neurodegenerative Disorders
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    Chapter 12 Neurodegeneration and Pathology in Epilepsy: Clinical and Basic Perspectives
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    Chapter 13 Prion Diseases
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    Chapter 14 Leukodystrophy: Basic and Clinical
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    Chapter 15 Traumatic Brain Injury as a Trigger of Neurodegeneration
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    Chapter 16 Cell Death Mechanisms of Neurodegeneration
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    Chapter 17 Neuroglia: Functional Paralysis and Reactivity in Alzheimer’s Disease and Other Neurodegenerative Pathologies
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    Chapter 18 Advances in Neuroimaging for Neurodegenerative Disease
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    Chapter 19 Gene Linkage and Systems Biology
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    Chapter 20 Biomarkers in Neurodegenerative Diseases
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    Chapter 21 Erratum
Attention for Chapter 7: Motoneuron Disease: Clinical
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Chapter title
Motoneuron Disease: Clinical
Chapter number 7
Book title
Neurodegenerative Diseases
Published in
Advances in neurobiology, July 2017
DOI 10.1007/978-3-319-57193-5_7
Pubmed ID
Book ISBNs
978-3-31-957191-1, 978-3-31-957193-5
Authors

Ilieva, Hristelina, Maragakis, Nicholas J., Hristelina Ilieva, Nicholas J. Maragakis

Abstract

ALS is a neurodegenerative disease in which the primary symptoms result in progressive neuromuscular weakness. Recent studies have highlighted that there is significant heterogeneity with regard to anatomical and temporal disease progression. Importantly, more recent advances in genetics have revealed new causative genes to the disease. New efforts have focused on the development of biomarkers that could aid in diagnosis, prognosis, and serve as pharmacodynamics markers. Although traditional pharmaceuticals continue to undergo trials for ALS, new therapeutic strategies including stem cell transplantation studies, gene therapies, and antisense therapies targeting some of the familial forms of ALS are gaining momentum.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 78 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 78 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 10 13%
Student > Master 9 12%
Student > Bachelor 9 12%
Student > Postgraduate 8 10%
Librarian 4 5%
Other 9 12%
Unknown 29 37%
Readers by discipline Count As %
Medicine and Dentistry 23 29%
Nursing and Health Professions 7 9%
Biochemistry, Genetics and Molecular Biology 4 5%
Social Sciences 3 4%
Immunology and Microbiology 2 3%
Other 8 10%
Unknown 31 40%