Limit search to available items
Book Cover
Author Knaap, Marjo S. van der.

Title Magnetic resonance of myelination and myelin disorders / Marjo S. van der Knaap, Jaap Valk ; with contributions by F. Barkhof [and others]
Edition 3rd ed
Published Berlin ; New York : Springer, ©2005


Description 1 online resource (xvi, 1084 pages) : illustrations
Contents 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 -- Mucopolysaccharidoses -- 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 I -- 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 Leukoencephalopathy of Neonates -- Neonatal Hypoglycemia -- Delayed Posthypoxic Leukoencephalopathy -- White Matter Lesions of the Elderly -- Subcortical Arteriosclerotic Encephalopathy -- Vasculitis -- Leukoencephalopathy and Dural Venous Fistula -- Leukoencephalopathy after Chemotherapy and/or Radiotherapy -- 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
Summary "This is the third edition of Magnetic Resonance of Myelination and Myelin Disorders, a standard text in the field. The book has been extensively revised and expanded to do justice to the rapid advances in MR technology, molecular biochemistry, and genetics and the discovery of new disease entities with prominent white matter involvement. Forty chapters have been added, and the number of illustrations has risen considerably. The ability to confirm the presence of genetic alterations in a number of disorders allows more advantageous presentation of the phenotypic variation as expressed in different MR patterns. Wider coverage is given to white matter disorders, hereditary and acquired, in the adult population."--Jacket
Analysis geneeskunde
public health
Medicine (General)
Geneeskunde (algemeen)
Bibliography Includes bibliographical references (pages 905-1073) and index
Notes Print version record
In Springer e-books
Subject Alexander disease.
Myelin sheath -- Diseases -- Magnetic resonance imaging
Magnetic resonance imaging.
Myelin sheath -- Diseases.
Demyelinating Diseases -- diagnosis
Demyelinating Diseases
Magnetic Resonance Imaging
Myelin Sheath -- physiology
PSYCHOLOGY -- Neuropsychology.
Magnetic resonance imaging
Alexander disease
Magnetic Resonance Imaging.
Form Electronic book
Author Valk, J.
Barkhof, Frederik, 1962-
Knaap, Marjo S. van der. Magnetic resonance of myelin, myelination, and myelin disorders
ISBN 9783540276609