000			06562nam a22003855i 4500
001			294457
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007			cr nn 008mamaa
008			150903s2005 gw | o |||| 0|eng d
020			_a9783540276609 _99783540276609
024	7		_a10.1007/3540276602 _2doi
035			_avtls000347006
039		9	_a201509030734 _bVLOAD _c201404121316 _dVLOAD _c201404091053 _dVLOAD _y201402070921 _zstaff
040			_aMX-SnUAN _bspa _cMX-SnUAN _erda
050		4	_aR895-920
100	1		_aKnaap, Marjo S. _eautor _9328042
245	1	0	_aMagnetic Resonance of Myelination and Myelin Disorders / _cby Marjo S. Knaap, Jaap Valk.
250			_aThird Edition.
264		1	_aBerlin, Heidelberg : _bSpringer Berlin Heidelberg, _c2005.
300			_axvI, 1084 páginas 647 illus in 3811 parts. _brecurso en línea.
336			_atexto _btxt _2rdacontent
337			_acomputadora _bc _2rdamedia
338			_arecurso en línea _bcr _2rdacarrier
347			_aarchivo de texto _bPDF _2rda
500			_aSpringer eBooks
505	0		_aMyelin 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.
520			_aThis 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.
590			_aPara consulta fuera de la UANL se requiere clave de acceso remoto.
700	1		_aValk, Jaap. _eautor _9328043
710	2		_aSpringerLink (Servicio en línea) _9299170
776	0	8	_iEdición impresa: _z9783540222866
856	4	0	_uhttp://remoto.dgb.uanl.mx/login?url=http://dx.doi.org/10.1007/3-540-27660-2 _zConectar a Springer E-Books (Para consulta externa se requiere previa autentificación en Biblioteca Digital UANL)
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