Rosenbergs Molecular and Genetic Basis of Neurological and Psychiatric Disease, Seventh Edition: Volume 2

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. Both volumes combined provide a comprehensive coverage on the neurogenetic foundation of neurological and psychiatric diseaseThis volume presents detailed coverage of disease mechanisms, and management for degenerative disorders, movement disorders, and muscle and neuromuscular junction disorders.Includes new chapters on the pharmacogenomics of Alzheimer's Disease and Epilepsy and the most recent updates in molecular genetics, focusing on pain genetics and muscular dystrophy INDICE: SECTION I. DEGENERATIVE DISORDERS1. Genomics of Alzheimer's disease2. Parkinson Disease and Related Disorders3. Frontotemporal dementia4. The Neuronal Ceroid-Lipofuscinoses (Batten Disease)SECTION II. MOVEMENT DISORDERS5. The Inherited ataxias6. Friedreich ataxia7. Ataxia-telangiectasia8. Dystonia9. Huntington’s Disease: Clinical Features, Disease Mechanisms, and Management10. The Hereditary Spastic ParaplegiasSECTION III. NEURO-ONCOLOGY11. GlioblastomaSECTION IV. NEUROCUTANEOUS DISORDERS12. Neurofibromatosis type 1 (NF1)13. Tuberous sclerosis complex14. Sturge-Weber syndrome15. Hemangioblastomas of the Central Nervous System16. Incontinentia pigmentiSECTION V. EPILEPSY17. Epilepsy Genetics - Considerations for Clinical Practice Today and for the FutureSECTION VI. LIPID METABOLISM DISORDERS18. Disorders of Lipid Metabolism19. Lipoprotein Disorders20. Cerebrotendinous xanthomatosisSECTION VII. WHITE MATTER DISEASES21. Multiple sclerosis22. Vanishing White Matter DiseaseSECTION VIII. NEUROPATHIES AND NEURONOPATHIES23. Amyotrophic Lateral Sclerosis24. Peripheral Neuropathies25. Spinal Muscular Atrophy26. Pain geneticsSECTION IX. MUSCLE AND NEUROMUSCULAR JUNCTION DISORDERS 27. Dystrophinopathies28. Limb-Girdle Muscular Dystrophy29. The Congenital Myopathies30. The Distal Myopathies31. Hereditary Inclusion-Body Myopathies32. The Myotonic Dystrophies33. Facioscapulohumeral Muscular Dystrophy34. Muscle Channelopathies: Periodic Paralyses and Nondystrophic Myotonias35. Congenital Myasthenic SyndromesSECTION X. STROKE36. Cerebral Vasculopathies37. Coagulopathies38. Sickle cell diseaseSection XI. Metal Metabolism Disorders39. Wilson Disease40. Menkes disease and other ATP7A disorders41. Neurodegeneration with Brain Iron Accumulation42. Pantothenate-kinase associated neurodegeneration43. Disorders of manganese transport44. AceruloplasminemiaSection XII. Vitamin Disorders45. Genetic and Dietary Influences on Life Span46. Vitamins: Cobalamin and Folate47. Disorders associated to Biotin and its Metabolism48. Disorders of Pyridoxine MetabolismSECTION XIII. PSYCHIATRIC DISEASE49. Unipolar Depression50. Bipolar Disorder51. Schizophrenia52. Obsessive-Compulsive Disorder53. Tourette Syndrome54. AddictionSECTION XIV. A NEUROLOGIC GENE MAP55. A Neurologic Gene Map

• ISBN: 978-0-443-19176-3
• Editorial: Academic Press
• Encuadernacion: Cartoné
• Páginas: 830
• Fecha Publicación: 01/07/2024
• Nº Volúmenes: 1
• Idioma: Inglés