Magnetic Resonance of Myelination and Myelin Disorders (MRI of Myelination & myelin disorders)

Myelin and White Matter....Pages 1-19
Classification of Myelin Disorders....Pages 20-24
Selective Vulnerability....Pages 25-36
Myelination and Retarded Myelination....Pages 37-65
Lysosomes and Lysosomal Disorders....Pages 66-73
Metachromatic Leukodystrophy....Pages 74-81
Multiple Sulfatase Deficiency....Pages 82-86
Globoid Cell Leukodystrophy: Krabbe Disease....Pages 87-95
GM 1 Gangliosidosis....Pages 96-102
GM 2 Gangliosidosis....Pages 103-111
Fabry Disease....Pages 112-118
Fucosidosis....Pages 119-122
Mucoplysaccharidoses....Pages 123-132
Free Sialic Acid Storage Disorder....Pages 133-136
Neuronal Ceroid Lipofuscinoses....Pages 137-146
Adult Polyglucosan Body Disease....Pages 147-150
Peroxisomes and Peroxisomal Disorders....Pages 151-153
Peroxisome Biogenesis Defects....Pages 154-166
Peroxisomal D-Bifunctional Protein Deficiency....Pages 167-171
Peroxisomal Acyl-CoA Oxidase Deficiency....Pages 172-175
X-Linked Adrenoleukodystrophy....Pages 176-190
Refsum Disease....Pages 191-194
Mitochondria and Mitochondrial Disorders....Pages 195-203
Mitochondrial Encephalopathy with Lactic Acidosis and Stroke-like Episodes....Pages 204-211
Leber Hereditary Optic Neuropathy....Pages 212-214
Kearns-Sayre Syndrome....Pages 215-220
Mitochondrial Neurogastrointestinal Encephalomyopathy....Pages 221-223
Leigh Syndrome and Mitochondrial Leukoencephalopathies....Pages 224-244
Pyruvate Carboxylase Deficiency....Pages 245-247
Multiple Carboxylase Deficiency....Pages 248-251
Cerebrotendinous Xanthomatosis....Pages 252-258
Cockayne Syndrome....Pages 259-267
Trichothiodystrophy with Photosensitivity....Pages 268-271
Pelizaeus-Merzbacher Disease and X-linked Spastic Paraplegia Type 2....Pages 272-280
18q − Syndrome....Pages 281-283
Phenylketonuria....Pages 284-293
Glutaric Aciduria Type 1....Pages 294-299
Propionic Acidemia....Pages 300-305
Nonketotic Hyperglycinemia....Pages 306-310
Maple Syrup Urine Disease....Pages 311-320
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency....Pages 321-325
Canavan Disease....Pages 326-333
 L -2-Hydroxyglutaric Aciduria....Pages 334-337
 D -2-Hydroxyglutaric Aciduria....Pages 338-341
Hyperhomocysteinemias....Pages 342-359
Urea Cycle Defects....Pages 360-368
Serine Synthesis Defect Caused by 3-Phosphoglycerate Dehydrogenase Deficiency....Pages 369-371
Molybdenum Cofactor Deficiency and Isolated Sulfite Oxidase Deficiency....Pages 372-376
Galactosemia....Pages 377-382
Sjögren-Larsson Syndrome....Pages 383-386
Lowe Syndrome....Pages 387-391
Wilson Disease....Pages 392-399
Menkes Disease....Pages 400-405
Fragile X Premutation....Pages 406-408
Hypomelanosis of Ito....Pages 409-411
Incontinentia Pigmenti....Pages 412-415
Alexander Disease....Pages 416-435
Giant Axonal Neuropathy....Pages 436-441
Megalencephalic Leukoencephalopathy with Subcortical Cysts....Pages 442-450
Congenital Muscular Dystrophies....Pages 451-468
Myotonic Dystrophy Type 1....Pages 469-472
Myotonic Dystrophy Type 2....Pages 473-475
X-linked Charcot-Marie-Tooth Disease....Pages 476-478
Oculodentodigital Dysplasia....Pages 479-480
Leukoencephalopathy with Vanishing White Matter....Pages 481-495
Aicardi-Goutières Syndrome....Pages 496-504
Leukoencephalopathy with Calcifications and Cysts....Pages 505-509
Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Elevated White Matter Lactate....Pages 510-518
Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum....Pages 519-525
Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids....Pages 526-529
Dentatorubropallidoluysian Atrophy....Pages 530-534
Cerebral Amyloid Angiopathy....Pages 535-540
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy....Pages 541-548
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy....Pages 549-551
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (Nasu-Hakola Disease)....Pages 552-556
Pigmentary Orthochromatic Leukodystrophy....Pages 557-558
Adult-Onset Autosomal Dominant Leukoencephalopathies....Pages 559-560
Inflammatory and Infectious Disorders....Pages 561-565
Multiple Sclerosis....Pages 566-603
Acute Disseminated Encephalomyelitis and Acute Hemorrhagic Encephalomyelitis....Pages 604-615
Acquired Immunodeficiency Syndrome....Pages 616-627
Progressive Multifocal Leukoencephalopathy....Pages 628-634
Brucellosis....Pages 635-639
Subacute Sclerosing Panencephalitis....Pages 640-644
Congenital and Perinatal Cytomegalovirus Infection....Pages 645-657
Whipple Disease....Pages 658-663
Toxic Encephalopathies....Pages 664-678
Iatrogenic Toxic Encephalopathies....Pages 679-683
Central Pontine and Extrapontine Myelinolysis....Pages 684-689
Hypernatremia....Pages 690-694
Marchiafava-Bignami Syndrome....Pages 695-698
Posterior Reversible Encephalopathy Syndrome....Pages 699-708
Langerhans Cell Histiocytosis....Pages 709-713
Post-Hypoxic-Ischemic Damage....Pages 714-717
Post-Hypoxic-Ischemic Encephalopathy of Neonates....Pages 718-748
Neonatal Hypoglycemia....Pages 749-754
Delayed Posthypoxic Leukoencephalopathy....Pages 755-758
White Matter Lesions of the Elderly....Pages 759-766
Subcortical Arteriosclerotic Encephalopathy....Pages 767-772
Vasculitis....Pages 773-800
Leukoencephalopathy and Dural Arteriovenous Fistulas....Pages 801-807
Leukoencephalopathy After Radiotherapy and Chemotherapy....Pages 808-817
Gliomatosis Cerebri....Pages 818-822
Diffuse Axonal Injury....Pages 823-831
Wallerian Degeneration and Myelin Loss Secondary to Neuronal and Axonal Degeneration....Pages 832-838
Diffusion-Weighted Imaging....Pages 839-853
Magnetization Transfer Imaging....Pages 854-858
Magnetic Resonance Spectroscopy: Basic Principles and Application in White Matter Disorders....Pages 859-880
Pattern Recognition in White Matter Disorders....Pages 881-904