Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease 6e(2Vol)

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
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 muscular 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
Sub-Section: Psychiatric Disease
36. Unipolar depression
37. Bipolar disorder
38. Schizophrenia
39. Obsessive 40. Tourette syndrome
41. Addiction

SECTION X. A NEUROLOGIC GENE MAP
42. A neurologic gene map