Research Catalog

Title

The molecular and genetic basis of neurologic and psychiatric disease / edited by Roger N. Rosenberg ... [et al.].

Publication

Philadelphia, PA : Butterworth-Heinemann, c2003.

Items in the Library & Off-site

Details

Additional Authors

Rosenberg, Roger N.

Description

xxi, 844 p. : ill.; 29 cm.

Uniform Title

Molecular and genetic basis of neurological disease.

Subject

• Nervous system > Diseases > Molecular aspects
• Nervous system > Diseases > Genetic aspects
• Molecular neurobiology
• Neurogenetics
• Nervous System Diseases > genetics
• Mental Disorders > genetics
• Molecular Biology

Note

• Rev. ed. of: The molecular and genetic basis of neurological disease. 2nd ed. 1997.

Bibliography (note)

• Includes bibliographical references and index.

Contents

Pt. I. General Concepts of Mechanisms of Disease -- Ch. 1. Triplet Repeat Disease: General Concepts and Mechanisms of Disease / Vicky L. Brandt and Huda Y. Zoghbi -- Ch. 2. Prions / Stanley B. Prusiner -- Ch. 3. Mendelian, Nonmendelian, Multigenic Inheritance, and Complex Traits / Ken Inoue and James R. Lupski -- Ch. 4. Degenerative Diseases and Protein Processing / Stanley B. Prusiner -- Ch. 5. Selected Genetically Engineered Models Relevant to Human Neurodegenerative Disease / Donald L. Price, David R. Borchelt, Michael K. Lee and Philip C. Wong -- Ch. 6. Gene Mapping to Gene Targeting: Application of Mouse Genetics to Human Disease / George A. Carlson -- Ch. 7. The Human Genome Project / Robert L. Nussbaum -- Ch. 8. Gene Therapy for Central Nervous System Disorders / Theodore Friedmann -- Ch. 9. Emerging Ethical Issues in Neurology, Psychiatry, and the Neurosciences / Arthur L. Caplan and Martha J. Farah -- Ch. 10. Genotype-Phenotype Correlations / Thomas D. Bird and Gerard D. Schellenberg -- Pt. II. Neurologic Diseases -- Ch. 11. Down Syndrome / Charles J. Epstein -- Ch. 12. Triplet Repeats: Genetics, Clinical Features, and Pathogenesis / Vicky L. Brandt and Huda Y. Zoghbi -- Ch. 13. Prion Diseases / Stephen J. DeArmond and Stanley B. Prusiner -- Ch. 14. The Mitochondrial Genome / Eric A. Schon -- Ch. 15. Mitochondrial Disorders Due to Mutations in the Mitochondrial Genome / Salvatore DiMauro and Eduardo Bonilla -- Ch. 16. Mitochondrial Disorders Due to Mutations in the Nuclear Genome / Michio Hirano -- Ch. 17. Mitochondria in Neurodegenerative Disorders / Giovanni Manfredi and M. Flint Beal -- Ch. 18. Peroxisomal Disorders / Hugo W. Moser -- Ch. 19. Gaucher Disease / Roscoe O. Brady and Raphael Schiffman -- Ch. 20. The Niemann-Pick Diseases / Roscoe O. Brady and Raphael Schiffman -- Ch. 21. The Gm2-Gangliosidoses / Edwin H. Kolodny and Orit Neudorfer -- Ch. 22. Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency: Sulfatide Lipidosis / Edwin H. Kolodny and Orit Neudorfer -- Ch. 23. Krabbe Disease: Globoid Cell Leukodystrophy / David A. Wenger -- Ch. 24. The Mucopolysaccharidoses and the Mucolipidoses / Reuben Matalon and Kimberlee Michals Matalon -- Ch. 25. Disorders of Glycoprotein Degradations: Sialidosis, Fucosidosis, Alpha-Mannosidosis, Beta-Mannosidosis, and Aspartylglycosaminuria / William G. Johnson -- Ch. 26. Beta-Galactosidase Deficiency: GM1 Gangaliosidosis, Morquio B Disease, and Galactosialidosis / Kunihiko Suzuki -- Ch. 27. Farber Disease: Acid Ceramidase Deficiency, Farber Lipogranulomatosis / Hugo W. Moser -- Ch. 28. Wolman Disease / Rita Alam and Frank M. Yatsu -- Ch. 29. Lysosomal Membrane Disorders - LAMP-2 Deficiency / Ichizo Nishino -- Ch. 30. Fabry Disease: [alpha]-Galactosidase A Deficiency / Robert J. Desnick -- Ch. 31. Schindler Disease: Deficient [alpha]-N-Acetylgalactosaminidase Activity / Robert J. Desnick and Detlev Schindler -- Ch. 32. Alzheimer's Disease / Dennis J. Selkoe -- Ch. 33. Frontotemporal Dementias / John Q. Trojanowski and Virginia M.-Y. Lee -- Ch. 34. Genetics of Movement Disorders / Juliette M. Harris and Stanley Fahn -- Ch. 35. The Inherited Ataxias / Roger N. Rosenberg and Henry L. Paulson -- Ch. 36. Caravan Disease / Reuben Matalon and Kimberlee Michals Matalon -- Ch. 37. Neuro-Oncology: The Neurofibromatoses / Christina A. Gurnett and David H. Gutmann -- Ch. 38. The Genetic Epilepsies / Marc A. Dichter and Jeffrey R. Buchhalter -- Ch. 39. Demyelinating Diseases / Stephen L. Hauser and Jorge R. Oksenberg -- Ch. 40. Peripheral Neuropathies / Steven S. Scherer, Kleopas A. Kleopa, Phillip F. Chance and Merrill D. Benson -- Ch. 41. The Molecular and Genetic Basis of Spinal Muscular Atrophies / Ching H. Wang -- Ch. 42. Dystrophinopathies / Eric P. Hoffman -- Ch. 43. Limb-Girdle Muscular Dystrophies / Rita Barresi and Kevin P. Campbell -- Ch. 44. The Congenital Myopathies / Heinz Jungbluth, Caroline A. Sewry and Francesco Muntoni -- Ch. 45. The Distal Myopathies / Ami K. Mankodi and Robert C. Griggs -- Ch. 46. Hereditary Inclusion Body Myopathies / Valerie Askanas and W. King Engel -- Ch. 47. The Mytonic Dystrophies / Richard T. Moxley III and Giovanni Meola -- Ch. 48. Facioscapulohumeral Dystrophy / Rabi Tawil -- Ch. 49. Ion Channel Disorders / Kleopas A. Kleopa and Robert L. Barchi -- Ch. 50. The Phakomatoses / Mia MacCollin -- Ch. 51. Lipoprotein Disorders / Mary J. Mallow and John P. Kane -- Ch. 52. Apolipoprotein E: Structure and Function in Lipid Metabolism and Neurobiology / Robert W. Mabley and Yadong Huang -- Ch. 53. Cerebrotendinous Xanthomatosis / Vladimir M. Berginer, Gerald Salen and Shailendra Patel -- Ch. 54. Glycogen Storage Diseases / Salvatore DiMauro, Serenella Servidei and Seiichi Tsujino -- Ch. 55. Disorders of Lipid Metabolism / Stefano DiDonato and Franco Taroni -- Ch. 56. Disorders of Galactose Metabolism / Louis J. Elsas II -- Ch. 57. Inborn Errors of Amino Acid Metabolism / William L. Myhan and Richard Harold Haas -- Ch. 58. Disorders of the Urea Cycle / Lewis J. Waber -- Ch. 59. Disorders of Glucose Transport / Darryl C. DeVivo, Dong Wang and Juan M. Pascual -- Ch. 60. Maple Syrup Urine Disease: Clinical and Biochemical Perspectives / David T. Chuang, Jacinta L. Chuang and Rody P. Cox -- Ch. 61. Metabolic Disorders-Congenital Disorders of Glycosylation / Marc C. Patterson -- Ch. 62. Disorders of Glutathione Metabolism / Ellinor Ristoff and Agne Larsson -- Ch. 63. Purines / William L. Nyhan -- Ch. 64. The Porphyrias / D. Montgomery Bissell -- Ch. 65. Friedrich's Ataxia and Iron Metabolism / Massimo Pandolfo -- Ch. 66. Disorders of Copper Metabolism: Wilson Disease and Menkes Disease / John H. Menkes -- Ch. 67. The Influence of [alpha]-Tocopherol, Calorie Restriction, and Genes on Life Span / Richard Mayeux -- Ch. 68. Vitamins: Cobolamine and Folate / Michael Shevell and David S. Rosenblatt -- Ch. 69. Disorders of Biotin Metabolism: Treatable Neurologic Syndromes / Barry Wolf -- Ch. 70. Psychiatric Diseases: Challenges in Psychiatric Genetics / Maja Bucan and Edward S. Brodkin -- Ch. 71. Depression / Kerry J. Ressler and Charles B. Nemeroff -- Ch. 72. Bipolar Disorder / Carol A. Mathews, Victor I. Reus and Nelson B. Freimer -- Ch. 73. Schizophrenia / David W. Volk and David A. Lewis -- Ch. 74. Obsessive-Compulsive Disorder and Tourette Syndrome / Paul J. Lombroso, Marcos T. Mercadente and Larry Scahill -- Ch. 75. Molecular and Genetic Bases of the Addictions / John C. Crabbe, Jr. and Kristine M. Wiren -- Ch. 76. Autism / M. L. Cuccaro, K. H. Lewis and Margaret A. Pericak-Vance -- Ch. 77. A Neurologic Gene Map / Roger N. Rosenberg, Anita Harding, Antonio V. Delgado-Escueta and Susan T. Iannoccone.

ISBN

0750673605

LCCN

2003040308

OCLC

• ocm51461169
• SCSB-4835098

Owning Institutions

Columbia University Libraries