Neurogenetics, Part II

Section V. Dementias26. The genetic landscape of Alzheimer disease27. Frontotemporal dementia28. The genetics of dementia with Lewy bodies29. Prion disease Section VI. Paroxysmal Disorders30. Genetics of epilepsy31. Genetics of migraine32. Periodic paralysis33. Episodic ataxias34. Disorders of sleep and circadian rhythms Section VII. Neuromuscular Disorders35. Facioscapulohumeral muscular dystrophy36. The genetics of congenital myopathies37. Genetic basis and phenotypic features of congenital myasthenic syndromes38. Spinal muscular atrophy39. Emerging understanding of the genotype: Phenotype relationship in amyotrophic lateral sclerosis40. Spinal and bulbar muscular atrophy41. Hereditary spastic paraplegia42. Neuropathy Section VIII. Diseases of White Matter and Demyelination 43. The spectrum of adult-onset heritable white matter disorders 44. Alexander disease45. Neurogenetics of Pelizaeus-Merzbacher disease46. Multiple sclerosis Section IX. Cerebrovascular Diseases47. CADASIL Section X. Major Adult Psychiatric Disorders48. Neuroepigenetics and addiction49. Genetic susceptibility in obsessive-compulsive disorder Section XI. Cancer and Phakomatoses50. Brain cancer genomics and epigenomics51. Neurofibromatosis type 152. Tuberous sclerosis complex53. Von Hippel-Lindau disease and Sturge-Weber syndrome