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Magnetic resonance of myelination and myelin disorders
Overview of attention for book
Table of Contents
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Book Overview
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Chapter 1
Myelin and White Matter
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Chapter 2
Classification of Myelin Disorders
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Chapter 3
Selective Vulnerability
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Chapter 4
Myelination and Retarded Myelination
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Chapter 5
Lysosomes and Lysosomal Disorders
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Chapter 6
Metachromatic Leukodystrophy
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Chapter 7
Multiple Sulfatase Deficiency
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Chapter 8
Globoid Cell Leukodystrophy: Krabbe Disease
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Chapter 9
GM 1 Gangliosidosis
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Chapter 10
GM 2 Gangliosidosis
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Chapter 11
Fabry Disease
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Chapter 12
Fucosidosis
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Chapter 13
Mucoplysaccharidoses
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Chapter 14
Free Sialic Acid Storage Disorder
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Chapter 15
Neuronal Ceroid Lipofuscinoses
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Chapter 16
Adult Polyglucosan Body Disease
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Chapter 17
Peroxisomes and Peroxisomal Disorders
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Chapter 18
Peroxisome Biogenesis Defects
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Chapter 19
Peroxisomal D-Bifunctional Protein Deficiency
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Chapter 20
Peroxisomal Acyl-CoA Oxidase Deficiency
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Chapter 21
X-Linked Adrenoleukodystrophy
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Chapter 22
Refsum Disease
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Chapter 23
Mitochondria and Mitochondrial Disorders
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Chapter 24
Mitochondrial Encephalopathy with Lactic Acidosis and Stroke-like Episodes
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Chapter 25
Leber Hereditary Optic Neuropathy
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Chapter 26
Kearns-Sayre Syndrome
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Chapter 27
Mitochondrial Neurogastrointestinal Encephalomyopathy
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Chapter 28
Leigh Syndrome and Mitochondrial Leukoencephalopathies
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Chapter 29
Pyruvate Carboxylase Deficiency
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Chapter 30
Multiple Carboxylase Deficiency
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Chapter 31
Cerebrotendinous Xanthomatosis
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Chapter 32
Cockayne Syndrome
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Chapter 33
Trichothiodystrophy with Photosensitivity
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Chapter 34
Pelizaeus-Merzbacher Disease and X-linked Spastic Paraplegia Type 2
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Chapter 35
18q − Syndrome
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Chapter 36
Phenylketonuria
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Chapter 37
Glutaric Aciduria Type 1
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Chapter 38
Propionic Acidemia
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Chapter 39
Nonketotic Hyperglycinemia
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Chapter 40
Maple Syrup Urine Disease
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Chapter 41
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
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Chapter 42
Canavan Disease
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Chapter 43
L -2-Hydroxyglutaric Aciduria
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Chapter 44
D -2-Hydroxyglutaric Aciduria
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Chapter 45
Hyperhomocysteinemias
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Chapter 46
Urea Cycle Defects
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Chapter 47
Serine Synthesis Defect Caused by 3-Phosphoglycerate Dehydrogenase Deficiency
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Chapter 48
Molybdenum Cofactor Deficiency and Isolated Sulfite Oxidase Deficiency
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Chapter 49
Galactosemia
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Chapter 50
Sjögren-Larsson Syndrome
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Chapter 51
Lowe Syndrome
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Chapter 52
Wilson Disease
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Chapter 53
Menkes Disease
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Chapter 54
Fragile X Premutation
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Chapter 55
Hypomelanosis of Ito
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Chapter 56
Incontinentia Pigmenti
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Chapter 57
Alexander Disease
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Chapter 58
Giant Axonal Neuropathy
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Chapter 59
Megalencephalic Leukoencephalopathy with Subcortical Cysts
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Chapter 60
Congenital Muscular Dystrophies
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Chapter 61
Myotonic Dystrophy Type 1
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Chapter 62
Myotonic Dystrophy Type 2
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Chapter 63
X-linked Charcot-Marie-Tooth Disease
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Chapter 64
Oculodentodigital Dysplasia
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Chapter 65
Leukoencephalopathy with Vanishing White Matter
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Chapter 66
Aicardi-Goutières Syndrome
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Chapter 67
Leukoencephalopathy with Calcifications and Cysts
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Chapter 68
Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Elevated White Matter Lactate
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Chapter 69
Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
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Chapter 70
Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
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Chapter 71
Dentatorubropallidoluysian Atrophy
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Chapter 72
Cerebral Amyloid Angiopathy
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Chapter 73
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Chapter 74
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Chapter 75
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (Nasu-Hakola Disease)
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Chapter 76
Pigmentary Orthochromatic Leukodystrophy
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Chapter 77
Adult-Onset Autosomal Dominant Leukoencephalopathies
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Chapter 78
Inflammatory and Infectious Disorders
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Chapter 79
Multiple Sclerosis
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Chapter 80
Acute Disseminated Encephalomyelitis and Acute Hemorrhagic Encephalomyelitis
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Chapter 81
Acquired Immunodeficiency Syndrome
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Chapter 82
Progressive Multifocal Leukoencephalopathy
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Chapter 83
Brucellosis
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Chapter 84
Subacute Sclerosing Panencephalitis
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Chapter 85
Congenital and Perinatal Cytomegalovirus Infection
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Chapter 86
Whipple Disease
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Chapter 87
Toxic Encephalopathies
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Chapter 88
Iatrogenic Toxic Encephalopathies
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Chapter 89
Central Pontine and Extrapontine Myelinolysis
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Chapter 90
Hypernatremia
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Chapter 91
Marchiafava-Bignami Syndrome
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Chapter 92
Posterior Reversible Encephalopathy Syndrome
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Chapter 93
Langerhans Cell Histiocytosis
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Chapter 94
Post-Hypoxic-Ischemic Damage
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Chapter 95
Post-Hypoxic-Ischemic Encephalopathy of Neonates
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Chapter 96
Neonatal Hypoglycemia
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Chapter 97
Delayed Posthypoxic Leukoencephalopathy
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Chapter 98
White Matter Lesions of the Elderly
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Chapter 99
Subcortical Arteriosclerotic Encephalopathy
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Chapter 100
Vasculitis
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Chapter 101
Leukoencephalopathy and Dural Arteriovenous Fistulas
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Chapter 102
Leukoencephalopathy After Radiotherapy and Chemotherapy
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Chapter 103
Gliomatosis Cerebri
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Chapter 104
Diffuse Axonal Injury
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Chapter 105
Wallerian Degeneration and Myelin Loss Secondary to Neuronal and Axonal Degeneration
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Chapter 106
Diffusion-Weighted Imaging
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Chapter 107
Magnetization Transfer Imaging
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Chapter 108
Magnetic Resonance Spectroscopy: Basic Principles and Application in White Matter Disorders
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Chapter 109
Pattern Recognition in White Matter Disorders
Overall attention for this book and its chapters
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Mentioned by
syllabi
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institution with syllabi
wikipedia
2
Wikipedia pages
Citations
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304
Dimensions
Readers on
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Mendeley
Book overview
1. Myelin and White Matter
2. Classification of Myelin Disorders
3. Selective Vulnerability
4. Myelination and Retarded Myelination
5. Lysosomes and Lysosomal Disorders
6. Metachromatic Leukodystrophy
7. Multiple Sulfatase Deficiency
8. Globoid Cell Leukodystrophy: Krabbe Disease
9. GM 1 Gangliosidosis
10. GM 2 Gangliosidosis
11. Fabry Disease
12. Fucosidosis
13. Mucoplysaccharidoses
14. Free Sialic Acid Storage Disorder
15. Neuronal Ceroid Lipofuscinoses
16. Adult Polyglucosan Body Disease
17. Peroxisomes and Peroxisomal Disorders
18. Peroxisome Biogenesis Defects
19. Peroxisomal D-Bifunctional Protein Deficiency
20. Peroxisomal Acyl-CoA Oxidase Deficiency
21. X-Linked Adrenoleukodystrophy
22. Refsum Disease
23. Mitochondria and Mitochondrial Disorders
24. Mitochondrial Encephalopathy with Lactic Acidosis and Stroke-like Episodes
25. Leber Hereditary Optic Neuropathy
26. Kearns-Sayre Syndrome
27. Mitochondrial Neurogastrointestinal Encephalomyopathy
28. Leigh Syndrome and Mitochondrial Leukoencephalopathies
29. Pyruvate Carboxylase Deficiency
30. Multiple Carboxylase Deficiency
31. Cerebrotendinous Xanthomatosis
32. Cockayne Syndrome
33. Trichothiodystrophy with Photosensitivity
34. Pelizaeus-Merzbacher Disease and X-linked Spastic Paraplegia Type 2
35. 18q − Syndrome
36. Phenylketonuria
37. Glutaric Aciduria Type 1
38. Propionic Acidemia
39. Nonketotic Hyperglycinemia
40. Maple Syrup Urine Disease
41. 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
42. Canavan Disease
43. L -2-Hydroxyglutaric Aciduria
44. D -2-Hydroxyglutaric Aciduria
45. Hyperhomocysteinemias
46. Urea Cycle Defects
47. Serine Synthesis Defect Caused by 3-Phosphoglycerate Dehydrogenase Deficiency
48. Molybdenum Cofactor Deficiency and Isolated Sulfite Oxidase Deficiency
49. Galactosemia
50. Sjögren-Larsson Syndrome
51. Lowe Syndrome
52. Wilson Disease
53. Menkes Disease
54. Fragile X Premutation
55. Hypomelanosis of Ito
56. Incontinentia Pigmenti
57. Alexander Disease
58. Giant Axonal Neuropathy
59. Megalencephalic Leukoencephalopathy with Subcortical Cysts
60. Congenital Muscular Dystrophies
61. Myotonic Dystrophy Type 1
62. Myotonic Dystrophy Type 2
63. X-linked Charcot-Marie-Tooth Disease
64. Oculodentodigital Dysplasia
65. Leukoencephalopathy with Vanishing White Matter
66. Aicardi-Goutières Syndrome
67. Leukoencephalopathy with Calcifications and Cysts
68. Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Elevated White Matter Lactate
69. Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
70. Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
71. Dentatorubropallidoluysian Atrophy
72. Cerebral Amyloid Angiopathy
73. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
74. Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
75. Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (Nasu-Hakola Disease)
76. Pigmentary Orthochromatic Leukodystrophy
77. Adult-Onset Autosomal Dominant Leukoencephalopathies
78. Inflammatory and Infectious Disorders
79. Multiple Sclerosis
80. Acute Disseminated Encephalomyelitis and Acute Hemorrhagic Encephalomyelitis
81. Acquired Immunodeficiency Syndrome
82. Progressive Multifocal Leukoencephalopathy
83. Brucellosis
84. Subacute Sclerosing Panencephalitis
85. Congenital and Perinatal Cytomegalovirus Infection
86. Whipple Disease
87. Toxic Encephalopathies
88. Iatrogenic Toxic Encephalopathies
89. Central Pontine and Extrapontine Myelinolysis
90. Hypernatremia
91. Marchiafava-Bignami Syndrome
92. Posterior Reversible Encephalopathy Syndrome
93. Langerhans Cell Histiocytosis
94. Post-Hypoxic-Ischemic Damage
95. Post-Hypoxic-Ischemic Encephalopathy of Neonates
96. Neonatal Hypoglycemia
97. Delayed Posthypoxic Leukoencephalopathy
98. White Matter Lesions of the Elderly
99. Subcortical Arteriosclerotic Encephalopathy
100. Vasculitis
101. Leukoencephalopathy and Dural Arteriovenous Fistulas
102. Leukoencephalopathy After Radiotherapy and Chemotherapy
103. Gliomatosis Cerebri
104. Diffuse Axonal Injury
105. Wallerian Degeneration and Myelin Loss Secondary to Neuronal and Axonal Degeneration
106. Diffusion-Weighted Imaging
107. Magnetization Transfer Imaging
108. Magnetic Resonance Spectroscopy: Basic Principles and Application in White Matter Disorders
109. Pattern Recognition in White Matter Disorders
Summary
Syllabi
Wikipedia
Dimensions citations
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Medicine