Research Catalog

Magnetic resonance of myelin, myelination, and myelin disorders / M.S. van der Knaap, J. Valk.

Title
Magnetic resonance of myelin, myelination, and myelin disorders / M.S. van der Knaap, J. Valk.
Author
Knaap, Marjo S. van der.
Publication
Berlin ; New York : Springer, [1995], ©1995.

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TextRequest in advance RC366 .V35 1995Off-site

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Additional Authors
Valk, J.
Description
558 pages : illustrations; 28 cm
Subject
  • Demyelinating Diseases > diagnosis
  • Demyelination
  • Magnetic Resonance Imaging
  • Myelin Sheath > physiology
  • Myelin sheath > Magnetic resonance imaging
  • Myelination
Note
  • Rev. ed. of: Magnetic resonance of myelin, myelination, and myelin disorders / J. Valk, M.S. van der Knaap. c1989.
Bibliography (note)
  • Includes bibliographical references and index.
Contents
  • 1. Myelin and White Matter -- 2. Classification of Myelin Disorders -- 3. Selective Vulnerability -- 4. Myelination and Retarded Myelination -- 5. Lysosomes and Lysosomal Disorders -- 6. Metachromatic Leukodystrophy -- 7. Multiple Sulfatase Deficiency -- 8. Globoid Cell Leukodystrophy: Krabbe's Disease -- 9. GM[subscript 1] Gangliosidosis -- 10. GM[subscript 2] Gangliosidosis -- 11. Fabry's Disease -- 12. Fucosidosis -- 13. Mucopolysaccharidoses -- 14. Peroxisomes and Peroxisomal Disorders -- 15. Zellweger Cerebrohepatorenal Syndrome, Neonatal Adrenoleukodystrophy, and Infantile Refsum Disease -- 16. Rhizomelic Chondrodysplasia Punctata -- 17. Zellweger-like Syndrome -- 18. Pseudo-neonatal Adrenoleukodystrophy, Trifunctional Protein Deficiency, and Pseudo-Zellweger Syndrome -- 19. X-linked Adrenoleukodystrophy -- 20. Mitochondria and Mitochondrial Disorders -- 21. Defects of Mitochondrial DNA -- 22. Leigh Syndrome -- 23. Pyruvate Carboxylase Deficiency --
  • 24. Cerebrotendinous Xanthomatosis -- 25. Refsum Disease -- 26. Nucleus, DNA, and DNA Repair -- 27. Cockayne's Disease -- 28. Pelizaeus-Merzbacher Disease -- 29. 18q Syndrome -- 30. Phenylketonuria -- 31. Glutaric Aciduria Type 1 -- 32. Propionic Acidemia -- 33. Hyperprolinemia -- 34. Nonketotic Hyperglycinemia -- 35. Maple Syrup Urine Disease -- 36. Canavan's Disease -- 37. L-2-Hydroxyglutaric Aciduria -- 38. Hyperhomocysteinemias -- 39. Urea Cycle Defects -- 40. Galactosemia -- 41. Sjogren-Larsson-Syndrome -- 42. Lowe Syndrome -- 43. Wilson Disease -- 44. Neuronal Ceroid Lipofuscinoses -- 45. Alexander's Disease -- 46. Myotonic Dystrophy -- 47. Congenital Muscular Dystrophy -- 48. Infantile-Onset Leukoencephalopathy with Swelling and a Discrepantly Mild Clinical Course -- 49. Childhood Ataxia with Diffuse Cerebral Hypomyelination --
  • 50. Leukoencephalopathy, Cerebral Calcifications, and Chronic Cerebrospinal Fluid Lymphocytosis (Aicardi-Goutieres Syndrome) -- 51. Inflammatory and Infectious Disorders -- 52. Multiple Sclerosis -- 53. Conditions Mimicking Multiple Sclerosis on MRI -- 54. Acute Disseminated Encephalomyelitis and Acute Hemorrhagic Encephalomyelitis -- 55. Acquired Immunodeficiency Syndrome -- 56. Progressive Multifocal Leukoencephalitis -- 57. Subacute Sclerosing Panencephalitis -- 58. Progressive Rubella Panencephalitis -- 59. Toxic Encephalopathy -- 60. Central Pontine and Extrapontine Myelinolysis -- 61. Marchiafava-Bignami Syndrome -- 62. Posthypoxic-Ischemic Damage -- 63. Posthypoxic-Ischemic Leukoencephalopathy of Neonates -- 64. Delayed Posthypoxic Leukoencephalopathy of Maturity -- 65. Subcortical Arteriosclerotic Encephalopathy -- 66. Vasculitis -- 67. Leukoencephalopathy After Chemotherapy and/or Radiotherapy -- 68. Cerebral Edema and Fluid Compartments in the CNS --
  • 69. Wallerian Degeneration and Myelin Loss Secondary to Neuronal and Axonal Degeneration -- 70. Pattern Recognition in White Matter Disorders -- 71. Magnetic Resonance Spectroscopy, Basic Principles, and Application in Myelin Disorders.
ISBN
3540592776 (alk. paper)
LCCN
95023696
Owning Institutions
Columbia University Libraries