Neurogenetics, Part II
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portes grátis
Neurogenetics, Part II
Geschwind, Daniel H.; Klein, Christine; Paulson, Henry L.
Elsevier Science & Technology
01/2018
480
Dura
Inglês
9780444640765
15 a 20 dias
1310
Descrição não disponível.
Section V. Dementias 26. The genetic landscape of Alzheimer disease 27. Frontotemporal dementia 28. The genetics of dementia with Lewy bodies 29. Prion disease
Section VI. Paroxysmal Disorders 30. Genetics of epilepsy 31. Genetics of migraine 32. Periodic paralysis 33. Episodic ataxias 34. Disorders of sleep and circadian rhythms
Section VII. Neuromuscular Disorders 35. Facioscapulohumeral muscular dystrophy 36. The genetics of congenital myopathies 37. Genetic basis and phenotypic features of congenital myasthenic syndromes 38. Spinal muscular atrophy 39. Emerging understanding of the genotype: Phenotype relationship in amyotrophic lateral sclerosis 40. Spinal and bulbar muscular atrophy 41. Hereditary spastic paraplegia 42. Neuropathy
Section VIII. Diseases of White Matter and Demyelination 43. The spectrum of adult-onset heritable white matter disorders 44. Alexander disease 45. Neurogenetics of Pelizaeus-Merzbacher disease 46. Multiple sclerosis
Section IX. Cerebrovascular Diseases 47. CADASIL
Section X. Major Adult Psychiatric Disorders 48. Neuroepigenetics and addiction 49. Genetic susceptibility in obsessive-compulsive disorder
Section XI. Cancer and Phakomatoses 50. Brain cancer genomics and epigenomics 51. Neurofibromatosis type 1 52. Tuberous sclerosis complex 53. Von Hippel-Lindau disease and Sturge-Weber syndrome
Section VI. Paroxysmal Disorders 30. Genetics of epilepsy 31. Genetics of migraine 32. Periodic paralysis 33. Episodic ataxias 34. Disorders of sleep and circadian rhythms
Section VII. Neuromuscular Disorders 35. Facioscapulohumeral muscular dystrophy 36. The genetics of congenital myopathies 37. Genetic basis and phenotypic features of congenital myasthenic syndromes 38. Spinal muscular atrophy 39. Emerging understanding of the genotype: Phenotype relationship in amyotrophic lateral sclerosis 40. Spinal and bulbar muscular atrophy 41. Hereditary spastic paraplegia 42. Neuropathy
Section VIII. Diseases of White Matter and Demyelination 43. The spectrum of adult-onset heritable white matter disorders 44. Alexander disease 45. Neurogenetics of Pelizaeus-Merzbacher disease 46. Multiple sclerosis
Section IX. Cerebrovascular Diseases 47. CADASIL
Section X. Major Adult Psychiatric Disorders 48. Neuroepigenetics and addiction 49. Genetic susceptibility in obsessive-compulsive disorder
Section XI. Cancer and Phakomatoses 50. Brain cancer genomics and epigenomics 51. Neurofibromatosis type 1 52. Tuberous sclerosis complex 53. Von Hippel-Lindau disease and Sturge-Weber syndrome
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addiction; Alexander disease; androgen receptor; animal; astrocyte; autoimmune disease; CAG/polyglutamine expansion; central core; centronuclear; channelopathies; chromatin; complex disease genetics; congenital; copy number variation (CNV); DNA methylation; DUX4; epigenetics; epilepsy; epileptic encephalopathies; facioscapulohumeral muscular dystrophyFSHD; febrile seizures; FSH dystrophy; GABRA1; gene regulation; genetics; genomewide association studies; genomewide association study; GFAP; glia; glutamate; GWAS; heritability; histone modifications; human; hypomyelination; immunology; KCNT2; leukodystrophy; model; mouse knockout; multiple sclerosis; mutation; myelin; myoclonic seizures; myopathies; nemaline; neuromuscular disease; obsessive-compulsive disorder (OCD); oligodendrocyte; remyelination; SCN1A; seizures; sequencing; SLC2A1; small noncoding RNAs; SMCHD1; spinal and bulbar muscular atrophy; structural; substance abuse disorder; testosterone
Section V. Dementias 26. The genetic landscape of Alzheimer disease 27. Frontotemporal dementia 28. The genetics of dementia with Lewy bodies 29. Prion disease
Section VI. Paroxysmal Disorders 30. Genetics of epilepsy 31. Genetics of migraine 32. Periodic paralysis 33. Episodic ataxias 34. Disorders of sleep and circadian rhythms
Section VII. Neuromuscular Disorders 35. Facioscapulohumeral muscular dystrophy 36. The genetics of congenital myopathies 37. Genetic basis and phenotypic features of congenital myasthenic syndromes 38. Spinal muscular atrophy 39. Emerging understanding of the genotype: Phenotype relationship in amyotrophic lateral sclerosis 40. Spinal and bulbar muscular atrophy 41. Hereditary spastic paraplegia 42. Neuropathy
Section VIII. Diseases of White Matter and Demyelination 43. The spectrum of adult-onset heritable white matter disorders 44. Alexander disease 45. Neurogenetics of Pelizaeus-Merzbacher disease 46. Multiple sclerosis
Section IX. Cerebrovascular Diseases 47. CADASIL
Section X. Major Adult Psychiatric Disorders 48. Neuroepigenetics and addiction 49. Genetic susceptibility in obsessive-compulsive disorder
Section XI. Cancer and Phakomatoses 50. Brain cancer genomics and epigenomics 51. Neurofibromatosis type 1 52. Tuberous sclerosis complex 53. Von Hippel-Lindau disease and Sturge-Weber syndrome
Section VI. Paroxysmal Disorders 30. Genetics of epilepsy 31. Genetics of migraine 32. Periodic paralysis 33. Episodic ataxias 34. Disorders of sleep and circadian rhythms
Section VII. Neuromuscular Disorders 35. Facioscapulohumeral muscular dystrophy 36. The genetics of congenital myopathies 37. Genetic basis and phenotypic features of congenital myasthenic syndromes 38. Spinal muscular atrophy 39. Emerging understanding of the genotype: Phenotype relationship in amyotrophic lateral sclerosis 40. Spinal and bulbar muscular atrophy 41. Hereditary spastic paraplegia 42. Neuropathy
Section VIII. Diseases of White Matter and Demyelination 43. The spectrum of adult-onset heritable white matter disorders 44. Alexander disease 45. Neurogenetics of Pelizaeus-Merzbacher disease 46. Multiple sclerosis
Section IX. Cerebrovascular Diseases 47. CADASIL
Section X. Major Adult Psychiatric Disorders 48. Neuroepigenetics and addiction 49. Genetic susceptibility in obsessive-compulsive disorder
Section XI. Cancer and Phakomatoses 50. Brain cancer genomics and epigenomics 51. Neurofibromatosis type 1 52. Tuberous sclerosis complex 53. Von Hippel-Lindau disease and Sturge-Weber syndrome
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
addiction; Alexander disease; androgen receptor; animal; astrocyte; autoimmune disease; CAG/polyglutamine expansion; central core; centronuclear; channelopathies; chromatin; complex disease genetics; congenital; copy number variation (CNV); DNA methylation; DUX4; epigenetics; epilepsy; epileptic encephalopathies; facioscapulohumeral muscular dystrophyFSHD; febrile seizures; FSH dystrophy; GABRA1; gene regulation; genetics; genomewide association studies; genomewide association study; GFAP; glia; glutamate; GWAS; heritability; histone modifications; human; hypomyelination; immunology; KCNT2; leukodystrophy; model; mouse knockout; multiple sclerosis; mutation; myelin; myoclonic seizures; myopathies; nemaline; neuromuscular disease; obsessive-compulsive disorder (OCD); oligodendrocyte; remyelination; SCN1A; seizures; sequencing; SLC2A1; small noncoding RNAs; SMCHD1; spinal and bulbar muscular atrophy; structural; substance abuse disorder; testosterone
