Magnetic Resonance of Myelination and Myelin Disorders
Autor Marjo S. van der Knaap, Jaap Valken Limba Engleză Hardback – 13 mai 2005
Preț: 3607.13 lei
Preț vechi: 3796.98 lei
-5% Nou
Puncte Express: 5411
Preț estimativ în valută:
690.29€ • 716.31$ • 576.97£
690.29€ • 716.31$ • 576.97£
Carte tipărită la comandă
Livrare economică 12-18 martie
Preluare comenzi: 021 569.72.76
Specificații
ISBN-13: 9783540222866
ISBN-10: 3540222863
Pagini: 1084
Ilustrații: XVI, 1084 p.
Dimensiuni: 203 x 276 x 63 mm
Greutate: 3.08 kg
Ediția:3rd ed. 2005
Editura: Springer Berlin, Heidelberg
Colecția Springer
Locul publicării:Berlin, Heidelberg, Germany
ISBN-10: 3540222863
Pagini: 1084
Ilustrații: XVI, 1084 p.
Dimensiuni: 203 x 276 x 63 mm
Greutate: 3.08 kg
Ediția:3rd ed. 2005
Editura: Springer Berlin, Heidelberg
Colecția Springer
Locul publicării:Berlin, Heidelberg, Germany
Public țintă
Professional/practitionerCuprins
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.
Recenzii
From the reviews of the third edition:
"This book provides a comprehensive, lucid description of particularly challenging clinical entities. With the third edition, the authors have greatly broadened an excellent reference; I would recommend this book for any practicing radiologist faced with challenging MR examinations of the adult or pediatric brain." (Doody's Publisher's Club; Reviewer: Edward H. Herskovits, University of Pennsylvania Medical Center).
"What a fabulous book! … The contents describe in great depth all white matter disorders known today, both adult and paediatric, both inherited and acquired. … This is most definitely a reference book – a terrific reference book. … It is highly recommended – a must for neuroradiology/neurology, both adult and paediatric. Both departments are incomplete without it. I have never so strongly endorsed the purchase of a book. I am both grateful and delighted to have had the opportunity to review it." (Shelley Renowden, Journal of Neurology, Vol. 253, 2006)
"This book provides a comprehensive, lucid description of particularly challenging clinical entities. With the third edition, the authors have greatly broadened an excellent reference; I would recommend this book for any practicing radiologist faced with challenging MR examinations of the adult or pediatric brain." (Doody's Publisher's Club; Reviewer: Edward H. Herskovits, University of Pennsylvania Medical Center).
"What a fabulous book! … The contents describe in great depth all white matter disorders known today, both adult and paediatric, both inherited and acquired. … This is most definitely a reference book – a terrific reference book. … It is highly recommended – a must for neuroradiology/neurology, both adult and paediatric. Both departments are incomplete without it. I have never so strongly endorsed the purchase of a book. I am both grateful and delighted to have had the opportunity to review it." (Shelley Renowden, Journal of Neurology, Vol. 253, 2006)
Caracteristici
Standard text on MR diagnosis of white matter disorders Authors are the internationally renowned experts in the field No competitive work on the market Extensive revision (40 additional chapters) Absolutely up-to-date Includes supplementary material: sn.pub/extras