Magnetic Resonance of Myelination and Myelin Disorders
Our thanks go to our colleagues at the VU Univer- Preface to the Third Edition sity Medical Center and to those in other hospitals Reading through the prefaces of the two previous edi- who referred their patients to us. We are indebted to tions,we can say that much of what was said there still all c...
| Κύριοι συγγραφείς: | , |
|---|---|
| Συγγραφή απο Οργανισμό/Αρχή: | |
| Μορφή: | Ηλεκτρονική πηγή Ηλ. βιβλίο |
| Γλώσσα: | English |
| Έκδοση: |
Berlin, Heidelberg :
Springer Berlin Heidelberg,
2005.
|
| Έκδοση: | Third Edition. |
| Θέματα: | |
| Διαθέσιμο Online: | Full Text via HEAL-Link |
Πίνακας περιεχομένων:
- Myelin and White Matter
- Classification of Myelin Disorders
- Selective Vulnerability
- Myelination and Retarded Myelination
- Lysosomes and Lysosomal Disorders
- Metachromatic Leukodystrophy
- Multiple Sulfatase Deficiency
- Globoid Cell Leukodystrophy: Krabbe Disease
- GM1 Gangliosidosis
- GM2 Gangliosidosis
- Fabry Disease
- Fucosidosis
- Mucoplysaccharidoses
- Free Sialic Acid Storage Disorder
- Neuronal Ceroid Lipofuscinoses
- Adult Polyglucosan Body Disease
- Peroxisomes and Peroxisomal Disorders
- Peroxisome Biogenesis Defects
- Peroxisomal D-Bifunctional Protein Deficiency
- Peroxisomal Acyl-CoA Oxidase Deficiency
- X-Linked Adrenoleukodystrophy
- Refsum Disease
- Mitochondria and Mitochondrial Disorders
- Mitochondrial Encephalopathy with Lactic Acidosis and Stroke-like Episodes
- Leber Hereditary Optic Neuropathy
- Kearns-Sayre Syndrome
- Mitochondrial Neurogastrointestinal Encephalomyopathy
- Leigh Syndrome and Mitochondrial Leukoencephalopathies
- Pyruvate Carboxylase Deficiency
- Multiple Carboxylase Deficiency
- Cerebrotendinous Xanthomatosis
- Cockayne Syndrome
- Trichothiodystrophy with Photosensitivity
- Pelizaeus-Merzbacher Disease and X-linked Spastic Paraplegia Type 2
- 18q? Syndrome
- Phenylketonuria
- Glutaric Aciduria Type 1
- Propionic Acidemia
- Nonketotic Hyperglycinemia
- Maple Syrup Urine Disease
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Canavan Disease
- L-2-Hydroxyglutaric Aciduria
- D-2-Hydroxyglutaric Aciduria
- Hyperhomocysteinemias
- Urea Cycle Defects
- Serine Synthesis Defect Caused by 3-Phosphoglycerate Dehydrogenase Deficiency
- Molybdenum Cofactor Deficiency and Isolated Sulfite Oxidase Deficiency
- Galactosemia
- Sjögren-Larsson Syndrome
- Lowe Syndrome
- Wilson Disease
- Menkes Disease
- Fragile X Premutation
- Hypomelanosis of Ito
- Incontinentia Pigmenti
- Alexander Disease
- Giant Axonal Neuropathy
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Congenital Muscular Dystrophies
- Myotonic Dystrophy Type 1
- Myotonic Dystrophy Type 2
- X-linked Charcot-Marie-Tooth Disease
- Oculodentodigital Dysplasia
- Leukoencephalopathy with Vanishing White Matter
- Aicardi-Goutières Syndrome
- Leukoencephalopathy with Calcifications and Cysts
- Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Elevated White Matter Lactate
- Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
- Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
- Dentatorubropallidoluysian Atrophy
- Cerebral Amyloid Angiopathy
- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (Nasu-Hakola Disease)
- Pigmentary Orthochromatic Leukodystrophy
- Adult-Onset Autosomal Dominant Leukoencephalopathies
- Inflammatory and Infectious Disorders
- Multiple Sclerosis
- Acute Disseminated Encephalomyelitis and Acute Hemorrhagic Encephalomyelitis
- Acquired Immunodeficiency Syndrome
- Progressive Multifocal Leukoencephalopathy
- Brucellosis
- Subacute Sclerosing Panencephalitis
- Congenital and Perinatal Cytomegalovirus Infection
- Whipple Disease
- Toxic Encephalopathies
- Iatrogenic Toxic Encephalopathies
- Central Pontine and Extrapontine Myelinolysis
- Hypernatremia
- Marchiafava-Bignami Syndrome
- Posterior Reversible Encephalopathy Syndrome
- Langerhans Cell Histiocytosis
- Post-Hypoxic-Ischemic Damage
- Post-Hypoxic-Ischemic Encephalopathy of Neonates
- Neonatal Hypoglycemia
- Delayed Posthypoxic Leukoencephalopathy
- White Matter Lesions of the Elderly
- Subcortical Arteriosclerotic Encephalopathy
- Vasculitis
- Leukoencephalopathy and Dural Arteriovenous Fistulas
- Leukoencephalopathy After Radiotherapy and Chemotherapy
- Gliomatosis Cerebri
- Diffuse Axonal Injury
- Wallerian Degeneration and Myelin Loss Secondary to Neuronal and Axonal Degeneration
- Diffusion-Weighted Imaging
- Magnetization Transfer Imaging
- Magnetic Resonance Spectroscopy: Basic Principles and Application in White Matter Disorders
- Pattern Recognition in White Matter Disorders.
