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The molecular and genetic basis of neurological disease

Author: Roger N Rosenberg
Publisher: Boston : Butterworth-Heinemann, ©1997.
Edition/Format:   Print book : English : 2nd edView all editions and formats
Summary:

A reference for neurologists and geneticists treating patients with genetic neurologic diseases. The text describes the progress being made in therapy for patients in several areas such as glycogen  Read more...

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Document Type: Book
All Authors / Contributors: Roger N Rosenberg
ISBN: 0750696680 9780750696685
OCLC Number: 35815221
Description: xix, 1430 pages : illustrations ; 29 cm
Contents: Contents: 1. Molecular Genetics and Neurologic Disease: An Introduction; 2. A Neurologic Gene Map; 3. Finding and Excluding Gene Locations by Linkage Analysis; 4. Gene Targeting; 5. Down Syndrome; 6. Fragile X Syndrome; 7. Molecular Biology of Prion Diseases; 8. Clinical and Neuropathologic Features of Prion Diseases; 9. Inherited Prion Diseases; 10. The Mitochondrial Genome; 11. Mitochondrial Encephalomyelopathies; 12. Mitochondrial Mechanisms of Aging; 13. Peroxisomal Disorders; 14. Refsum Disease; 15. The Mucopolysaccharidoses and the Mucolipidoses; 16. Disorders of Glycoprotein Degradation; 17. Wolman Disease; 18. Ceramidase Deficiency: Farber Lipogranulomatoses; 19. The Niemann-Pick Disease Group; 20. Glucosyceramide Lipidosis: Gaucher Disease; 21. Krabbe Disease (Globoid Cell Leukodystrophy); 22. Metachromatic Leukodystrophy and Multiple Sulfatase Deficiency; 23. Fabry Disease: Alpha-Galactosidase A Deficiency; 24. Schindler Disease: Deficient Alpha-N-Acetylgalactosamindase Activity; 25. Beta-Galactosidase Deficiency: GM1 Gangliosidosis, Morquio B Disease, and Galactosialidosis; 26. The GM2 Gangliosidoses; 27. Canavan Disease; 28. The Hereditary Ataxias; 29. Huntington Disease; 30. Inherited Disorders of the Basal Ganglia; 31. Alzheimer Disease: Clinical and Genetic Features; 32. Cellular and Molecular Biology of Amyloid and Alzheimer Disease; 33. Cellular and Molecular Biological Aspects of Tau and Alzheimer Disease; 34. Inherited Multiple Sclerosis; 35. Oncogenes and Neuro-Oncology; 36. Tumors of Neuronal Cell Origin; 37. Tumor Suppressor Genes and the Nervous System; 38. The Clinical and Molecular Genetics of Neurofibromitosis I and II; 39. Myotonia Congenita; 40. The Periodic Paralyses; 41. Malignant Hyperthermia and Central Core Disease; 42. Episodic Ataxia and Myokymia; 43. Genetic Epilepsies; 44. Spinal Muscular Atrophy; 45. Inherited ALS; 46. Inherited Demyelinating Neuropathy; 47. Inherited Axonal Neuropathy; 48. Familial Amyloidotic Neuropathy; 49. Congenital Myopathies; 50. Dystrophinopathi
Responsibility: edited by Roger N. Rosenberg [and others].

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