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

Rosenberg's Molecular and Genetic Basis of Neurologic and Psychiatric Disease, Sixth Edition: Volume Two 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. A favorite of over three generations of students, clinicians and scholars, this new edition retains and expands on the informative, concise and critical tone of the first 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. The content covers all aspects essential to the practice of neurogenetics to inform clinical diagnosis, treatment and genetic counseling. Provides comprehensive coverage on the neurogenetic foundation of neurological and psychiatric diseasePresents detailed coverage of genomics, animal models and diagnostic methods, with new coverage on evaluating patients with biochemical abnormalities or gene mutationsIncludes new chapters on the pharmacogenomics of epilepsy and the most recent updates in molecular genetics, focusing on neurodegenerative and psychiatric diseases INDICE: SECTION I. DEGENERATIVE DISORDERS 1. Genomics of Alzheimer's disease 2. Parkinson 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. Ataxia-telangiectasia 8. Dystonia 9. Huntington's Disease: Clinical Features, Disease Mechanisms, and Management 10. The Hereditary Spastic Paraplegias SECTION III. NEURO-ONCOLOGY 11. Glioblastoma SECTION IV. NEUROCUTANEOUS DISORDERS 12. Neurofibromatosis type 1 (NF1) 13. Tuberous Sclerosis Complex 14. Sturge-Weber Syndrome 15. Hemangioblastomas of the Central Nervous System 16. Incontinentia pigmenti SECTION V. EPILEPSY 17. Epilepsy Genetics - Considerations for Clinical Practice Today and for the Future SECTION VI. WHITE MATTER DISEASES 18. Multiple sclerosis 19. Vanishing White Matter Disease SECTION VII. NEUROPATHIES AND NEURONOPATHIES 20. Amyotrophic Lateral Sclerosis 21. Peripheral Neuropathies 22. Spinal Muscular Atrophy 23. Pain Genetics SECTION VIII. MUSCLE AND NEUROMUSCULAR JUNCTION DISORDERS 24. Dystrophinopathies 25. Limb-Girdle Muscular Dystrophy 26. The Congenital Myopathies 27. The Distal Myopathies 28. Hereditary Inclusion-Body Myopathies 29. The Myotonic Dystrophies 30. Facioscapulohumeral Dystrophy 31. Muscle Channelopathies: Periodic Paralyses and Nondystrophic Myotonias 32. Congenital Myasthenic Syndromes SECTION IX. STROKE 33. Cerebral Vasculopathies 34. Coagulopathies 35. Sickle Cell Disease SECTION X. PSYCHIATRIC DISEASE 36. Unipolar Depression 37. Bipolar Disorder 38. Schizophrenia 39. Obsessive-Compulsive Disorder 40. Tourette Syndrome 41. Addiction SECTION XI. A NEUROLOGIC GENE MAP 42. A Neurologic Gene Map

• ISBN: 978-0-12-813866-3
• Editorial: Academic Press
• Encuadernacion: Cartoné
• Páginas: 750
• Fecha Publicación: 01/06/2020
• Nº Volúmenes: 1
• Idioma: Inglés