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Genetic Neuromuscular Disorders

Overview of attention for book
Cover of 'Genetic Neuromuscular Disorders'

Table of Contents

  1. Altmetric Badge
    Book Overview
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    Chapter 1 Duchenne Muscular Dystrophy
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    Chapter 2 Duchenne Muscular Dystrophy Carrier
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    Chapter 3 Becker Muscular Dystrophy
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    Chapter 4 Emery-Dreifuss Muscular Dystrophy Type 1
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    Chapter 5 Emery-Dreifuss Muscular Dystrophy Type 2
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    Chapter 6 Limb-Girdle Muscular Dystrophy Type 1B
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    Chapter 7 Limb-Girdle Muscular Dystrophy Type 1C
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    Chapter 8 Limb-Girdle Muscular Dystrophy Type 1F
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    Chapter 9 Limb-Girdle Muscular Dystrophy Type 2A
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    Chapter 10 Limb-Girdle Muscular Dystrophy Type 2B
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    Chapter 11 Limb-Girdle Muscular Dystrophy Type 2C
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    Chapter 12 Limb-Girdle Muscular Dystrophy Type 2D
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    Chapter 13 Limb-Girdle Muscular Dystrophy Type 2E
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    Chapter 14 Limb-Girdle Muscular Dystrophy Type 2F
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    Chapter 15 Limb-Girdle Muscular Dystrophy Type 2I
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    Chapter 16 Limb-Girdle Muscular Dystrophy Type 2K
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    Chapter 17 Limb-Girdle Muscular Dystrophy Type 2N
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    Chapter 18 Congenital Muscular Dystrophy Type 1A
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    Chapter 19 Congenital Muscular Dystrophy Type 1C
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    Chapter 20 Congenital Muscular Dystrophy with Rigid Spine
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    Chapter 21 Congenital Muscular Dystrophy with Integrin-Alpha-7 Deficiency
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    Chapter 22 Congenital Muscular Dystrophy, Ullrich Disease
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    Chapter 23 Bethlem Myopathy
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    Chapter 24 Facioscapulohumeral Muscular Dystrophy Type 1A
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    Chapter 25 Facioscapulohumeral Muscular Dystrophy Type 2
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    Chapter 26 Congenital Multiminicore Myopathy
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    Chapter 27 Congenital Central Core Myopathy with Malignant Hyperthermia
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    Chapter 28 Congenital Centronuclear Myopathy Type 1
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    Chapter 29 Congenital Hyaline Body Myopathy
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    Chapter 30 Congenital Myotubular Myopathy
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    Chapter 31 Congenital Nemaline Myopathy Type 2
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    Chapter 32 Congenital Fiber-Type Disproportion Type 1
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    Chapter 33 Congenital Fiber-Type Disproportion
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    Chapter 34 Congenital Myofibrillar Myopathy Type 1
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    Chapter 35 Congenital Myofibrillar Myopathy Type 6
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    Chapter 36 Congenital Tubular Aggregate Myopathy
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    Chapter 37 Hereditary Inclusion Body Myopathy Type 2
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    Chapter 38 Myotonic Dystrophy Type 1, Steinert Disease
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    Chapter 39 Congenital Myotonic Dystrophy
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    Chapter 40 Myotonic Dystrophy Type 2, Proximal Myotonic Myopathy
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    Chapter 41 Congenital Myotonia, Thomsen Disease
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    Chapter 42 Hyperkalemic Periodic Paralysis
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    Chapter 43 Hypokalemic Periodic Paralysis Type 1
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    Chapter 44 Slow-Channel Congenital Myasthenic Syndrome
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    Chapter 45 Congenital Myasthenic Syndrome
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    Chapter 46 Brody Disease
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    Chapter 47 Glycogenosis Type 2, Pompe Disease
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    Chapter 48 Glycogenosis Type 3, Cori-Forbes Disease
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    Chapter 49 Glycogenosis Type 5, McArdle Disease
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    Chapter 50 Danon Disease
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    Chapter 51 Kearns-Sayre Syndrome
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    Chapter 52 Chronic Progressive External Ophthalmoplegia
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    Chapter 53 MELAS (Myopathy, Encephalopathy, Lactic Acidosis, Stroke-like Episodes)
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    Chapter 54 Leigh Syndrome due to COX Deficiency
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    Chapter 55 Mitochondrial Encephalomyopathy with COX Deficiency
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    Chapter 56 Coenzyme Q10 Deficiency
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    Chapter 57 Multiple Symmetric Lipomatosis
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    Chapter 58 NARP (Neuropathy, Ataxia, Retinitis Pigmentosa)
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    Chapter 59 SANDO (Sensory Ataxic Neuropathy, Dysarthria, Ophthalmoparesis)
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    Chapter 60 Systemic Primary Carnitine Deficiency
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    Chapter 61 Neutral Lipid Storage Disease with Ichthyosis, Chanarin-Dorfman Syndrome
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    Chapter 62 Neutral Lipid Storage Disease with Myopathy
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    Chapter 63 Multiple Acyl-CoA Dehydrogenase Deficiency
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    Chapter 64 Carnitine Palmitoyltransferase II Deficiency
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    Chapter 65 Niemann-Pick Disease Type C1
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    Chapter 66 Spinal Muscular Atrophy Type 1, Werdnig-Hoffmann Disease
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    Chapter 67 Spinal Muscular Atrophy Type 2, Werdnig-Hoffmann Disease
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    Chapter 68 Spinal Muscular Atrophy Type 3, Kugelberg-Welander Disease
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    Chapter 69 Spinal Bulbar Muscular Atrophy, Kennedy Disease
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    Chapter 70 Charcot-Marie-Tooth Disease, Type 1A
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    Chapter 71 Charcot-Marie-Tooth Disease, Type 1B
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    Chapter 72 Charcot-Marie-Tooth Disease, Neuronal Type
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    Chapter 73 Charcot-Marie-Tooth Disease, Type 4A
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    Chapter 74 Charcot-Marie-Tooth Neuropathy with Pyramidal Features
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    Chapter 75 Charcot-Marie-Tooth Disease, Type X1
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    Chapter 76 Distal Spinal Muscular Atrophy
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    Chapter 77 Hereditary Neuropathy with Pressure Palsies
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    Chapter 78 Friedreich’s Ataxia
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    Chapter 79 Spastic Ataxia, Charlevoix-Saguenay Type
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    Chapter 80 Ataxia-Telangiectasia, Louis-Bar Syndrome
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    Chapter 81 Spastic Paraparesis Type 4
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    Chapter 82 Spastic Paraparesis Type 7
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    Chapter 83 Optic Atrophy Plus Syndrome
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    Chapter 84 Amyotrophic Lateral Sclerosis Type 1
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    Chapter 85 Amyotrophic Lateral Sclerosis
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Title
Genetic Neuromuscular Disorders
Published by
Springer International Publishing, August 2014
DOI 10.1007/978-3-319-07500-6
ISBNs
978-3-31-907499-3, 978-3-31-907500-6
Authors

Angelini, Corrado

X Demographics

X Demographics

The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 18 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 18 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 22%
Professor 4 22%
Student > Bachelor 2 11%
Student > Ph. D. Student 2 11%
Other 1 6%
Other 1 6%
Unknown 4 22%
Readers by discipline Count As %
Medicine and Dentistry 6 33%
Biochemistry, Genetics and Molecular Biology 2 11%
Nursing and Health Professions 2 11%
Neuroscience 2 11%
Agricultural and Biological Sciences 2 11%
Other 1 6%
Unknown 3 17%