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Inherited Neuromuscular Diseases

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Cover of 'Inherited Neuromuscular Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 Pathology and Diagnosis of Muscular Dystrophies
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    Chapter 2 Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations
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    Chapter 3 Genetics and Pathogenesis of Distal Muscular Dystrophies
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    Chapter 4 Phenotype Variations in Early Onset Pompe Disease: Diagnosis and Treatment Results with Myozyme®
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    Chapter 5 Inherited Neuromuscular Diseases
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    Chapter 6 Mitochondrial Diseases: A Cross-Talk Between Mitochondrial and Nuclear Genomes
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    Chapter 7 Mitochondrial Disorders Due to Nuclear OXPHOS Gene Defects
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    Chapter 8 Coenzyme Q10 Deficiencies in Neuromuscular Diseases
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    Chapter 9 The Role of Mitochondrial Network Dynamics in the Pathogenesis of Charcot-Marie-Tooth Disease
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    Chapter 10 Pathogenesis and Treatment of Mitochondrial Disorders
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    Chapter 11 Biology of Peripheral Inherited Neuropathies: Schwann Cell Axonal Interactions
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    Chapter 12 Phenotype and Clinical Evolution of Charcot-Marie-Tooth Disease Type 1A Duplication
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    Chapter 13 Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromes.
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    Chapter 14 Natural History and Treatment of Peripheral Inherited Neuropathies
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    Chapter 15 Spinal Muscular Atrophy During Human Development: Where Are the Early Pathogenic Findings?
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    Chapter 16 Spinal Muscular Atrophy
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    Chapter 17 Friedreich Ataxia: An Update on Animal Models, Frataxin Function and Therapies
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    Chapter 18 Genetics and Pathogenesis of Inherited Ataxias and Spastic Paraplegias
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72 Mendeley
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Inherited Neuromuscular Diseases
Published by
Springer, Dordrecht, October 2009
DOI 10.1007/978-90-481-2813-6
978-9-04-812812-9, 978-9-04-812813-6, 978-9-40-073056-4

Carmen Espinós, Vicente Felipo, Francesc Palau

Mendeley readers

The data shown below were compiled from readership statistics for 72 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 72 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 3 4%
Researcher 2 3%
Student > Master 2 3%
Student > Bachelor 2 3%
Student > Ph. D. Student 1 1%
Other 1 1%
Unknown 61 85%
Readers by discipline Count As %
Medicine and Dentistry 4 6%
Neuroscience 3 4%
Biochemistry, Genetics and Molecular Biology 2 3%
Nursing and Health Professions 1 1%
Agricultural and Biological Sciences 1 1%
Other 0 0%
Unknown 61 85%