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LIBRERIA STUDIUM
Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease - Volume 2
7th Edition
Rosenberg, Pascual
Editore
Elsevier
Anno
2024
Pagine
1156
ISBN
9780443191763
175,00 €
DA SCONTARE
| Founding Director, Alzheimer’s Disease Center Head, Section on Memory and Behavioral Neurology, University of Texas Southwestern Medical Center, Dallas, Texas, USA; Juan M. Pascual, Dept Neurology and Neurotherapeutics, Physiology and Pediatrics and McDermott Ctr for Human Growth and Dev/Ctr for Human Genetics, Univ of Texas Southwestern Medical Ctr, Dallas, TX, USA | ||
| Description: Rosenberg’s Molecular and Genetic Basis of Neurologic and Psychiatric Disease, Seventh Edition provides a comprehensive introduction and reference to the foundations and practical aspects relevant to the majority of neurologic and psychiatric disease. This updated volume focuses on degenerative disorders, movement disorders, neuro-oncology, neurocutaneous disorders, epilepsy, white matter diseases, neuropathies and neuronopathies, muscle and neuromuscular junction disorders, stroke, psychiatric disease, and a neurologic gene map. This volume includes new chapters on Von Hippel-Lindau disease, antisocial and violent behavior and Autism. A favorite of over four generations of students, clinicians and scholars, this new edition retains and expands on the informative, concise and critical tone of the previous edition. This is an essential reference for general medical practitioners, neurologists, psychiatrists, geneticists, related professionals, and for the neuroscience and neurology research community at large. |
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| Table Of Contents: | ||
| Table Of Contents: | ||
| SECTION I. DEGENERATIVE DISORDERS 1. Genomics of alzheimer's disease 2. Parkinson’s disease and related disorders 3. Frontotemporal dementia 4. The neuronal ceroid-lipofuscinoses (Batten disease) SECTION II. MOVEMENT DISORDERS 5. The inherited ataxias 6. Friedreich ataxia 7. Clinical and molecular findings in Ataxia-Telangiectasia 8. Dystonia 9. Huntington’s Disease 10. The hereditary spastic paraplegias SECTION III. NEURO-ONCOLOGY 11. Glioblastoma SECTION IV. NEUROCUTANEOUS DISORDERS 12. Neurofibromatosis type 1 13. Tuberous sclerosis complex 14. Sturge-Weber syndrome 15. Hemangioblastomas of the central nervous system 16. Incontinentia pigmenti SECTION V. EPILEPSY 17. Epilepsy genetics in clinical practice today and for the future SECTION VI. LIPID METABOLISM DISORDERS 18. Disorders of lipid metabolism 19. Lipoprotein disorders 20. Cerebrotendinous xanthomatosis SECTION VII. WHITE MATTER DISEASES 21. Multiple sclerosis 22. Vanishing white matter SECTION VIII. NEUROPATHIES AND NEURONOPATHIES 23. Amyotrophic lateral Sclerosis 24. Peripheral neuropathies 25. Spinal muscular atrophy 26. Pain genetics SECTION IX. MUSCLE AND NEUROMUSCULAR JUNCTION DISORDERS 27. Dystrophinopathies 28. Limb-girdle muscular dystrophy 29. The congenital myopathies 30. The distal myopathies 31. Hereditary inclusion-body myopathies 32. The myotonic dystrophies 33. Facioscapulohumeral muscular dystrophy 34. Muscle channelopathies: periodic paralyses and nondystrophic myotonias 35. Congenital myasthenic syndromes SECTION X. STROKE 36. Cerebral vasculopathies 37. Coagulopathies 38. Sickle cell disease SECTION XI. METAL METABOLISM DISORDERS 39. Wilson disease 40. Menkes disease and other ATP7A disorders 41. Neurodegeneration with brain iron accumulation 42. Pantothenate-kinase associated neurodegeneration 43. Disorders of manganese transport 44. Aceruloplasminemia SECTION XII. VITAMIN DISORDERS 45. Genetic and dietary influences on life span 46. Vitamins: cobalamin and folate 47. Inherited disorders associated to biotin and its metabolism 48. Disorders of pyridoxine metabolism SECTION XIII. PSYCHIATRIC DISEASE 49. Unipolar depression 50. Bipolar disorder 51. Schizophrenia 52. Obsessive-compulsive disorder 53. Tourette syndrome 54. Addiction SECTION XIV. A NEUROLOGIC GENE MAP 55. A neurologic gene map |
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