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Magnetic Resonance of Myelination and Myelin Disorders / by Marjo S. Knaap, Jaap Valk
Contributor(s): Resource type: Ressourcentyp: Buch (Online)Book (Online)Language: English Series: SpringerLink BücherPublisher: Berlin, Heidelberg : Springer-Verlag Berlin Heidelberg, 2005Edition: Third EditionDescription: Online-Ressource (XVI, 1084 p. 647 illus in 3811 parts, digital)ISBN:- 9783540276609
- 616.0757
- 616.8/5607548 22
- 610
- R895-920
- RC366
- WL 141
Contents:
Summary: No description available.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 differPPN: PPN: 1647315522Package identifier: Produktsigel: ZDB-1-SMI | ZDB-2-SME
Preliminary; 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; GM2 Gangliosidosis; Free Sialic Acid Storage Disorder; Peroxisomal Acyl-CoA Oxidase Deficiency; X-Linked Adrenoleukodystrophy; Mitochondria and Mitochondrial Disorders; Mitochondrial Encephalopathy with Lactic Acidosis and Stroke-like Episodes; Leber Hereditary Optic Neuropathy
Mitochondrial Neurogastrointestinal EncephalomyopathyLeigh 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
HyperhomocysteinemiasUrea 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 DysplasiaAicardi-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; Brucellosis; Subacute Sclerosing Panencephalitis; Congenital and Perinatal Cytomegalovirus Infection; Whipple Disease; Toxic Encephalopathies; Iatrogenic Toxic Encephalopathies; Central Pontine and Extrapontine Myelinolysis
Hypernatremia
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