Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease, Seventh Edition
eBook - ePub

Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease, Seventh Edition

Volume 1

  1. English
  2. ePUB (mobile friendly)
  3. Available on iOS & Android
eBook - ePub

Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease, Seventh Edition

Volume 1

About this book

Rosenberg's Molecular and Genetic Basis of Neurologic and Psychiatric Disease, Seventh Edition, provides a comprehensive introduction and reference to the foundations and key practical aspects relevant to neurologic and psychiatric disease. This volume has been thoroughly revised and includes newly commissioned chapters on ethics, genetic counselling and genet therapy for the central nervous system disorders. A favorite of over four generations of students, clinicians and scholars, this new edition retains and expands the informative, concise and critical tone of the previous edition. This is an essential reference for general medical practitioners, neurologists, psychiatrists, geneticists, and 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 disease - This volume provides a detailed introduction on both the clinical and basic research implications of molecular and genetics surrounding the brain - Includes new chapters on genomics of human neurological disorders, CRISPR and genome engineering

Frequently asked questions

Yes, you can cancel anytime from the Subscription tab in your account settings on the Perlego website. Your subscription will stay active until the end of your current billing period. Learn how to cancel your subscription.
At the moment all of our mobile-responsive ePub books are available to download via the app. Most of our PDFs are also available to download and we're working on making the final remaining ones downloadable now. Learn more here.
Perlego offers two plans: Essential and Complete
  • Essential is ideal for learners and professionals who enjoy exploring a wide range of subjects. Access the Essential Library with 800,000+ trusted titles and best-sellers across business, personal growth, and the humanities. Includes unlimited reading time and Standard Read Aloud voice.
  • Complete: Perfect for advanced learners and researchers needing full, unrestricted access. Unlock 1.4M+ books across hundreds of subjects, including academic and specialized titles. The Complete Plan also includes advanced features like Premium Read Aloud and Research Assistant.
Both plans are available with monthly, semester, or annual billing cycles.
We are an online textbook subscription service, where you can get access to an entire online library for less than the price of a single book per month. With over 1 million books across 1000+ topics, we’ve got you covered! Learn more here.
Look out for the read-aloud symbol on your next book to see if you can listen to it. The read-aloud tool reads text aloud for you, highlighting the text as it is being read. You can pause it, speed it up and slow it down. Learn more here.
Yes! You can use the Perlego app on both iOS or Android devices to read anytime, anywhere — even offline. Perfect for commutes or when you’re on the go.
Please note we cannot support devices running on iOS 13 and Android 7 or earlier. Learn more about using the app.
Yes, you can access Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease, Seventh Edition by Roger N. Rosenberg,Juan M. Pascual in PDF and/or ePUB format, as well as other popular books in Biological Sciences & Genetics & Genomics. We have over one million books available in our catalogue for you to explore.

Table of contents

  1. Rosenberg’s Molecular and Genetic Basis of Neurological and Psychiatric Disease, Volume 1
  2. Chapter 1 Mendelian, non-Mendelian, multigenic inheritance, and epigenetics
  3. Chapter 2 Precision medicine in neurology
  4. Chapter 3 Epigenomics of neurological disorders
  5. Chapter 4 What genes can and cannot do
  6. Chapter 5 Genotype–phenotype considerations in neurogenetic disease
  7. Chapter 6 Immunogenetics of neurological disease
  8. Chapter 7 Pharmacogenomic approaches to the treatment of sporadic Alzheimer’s disease
  9. Chapter 8 Application of mouse genetics to human disease: generation and analysis of mouse models
  10. Chapter 9 DNA sequencing and other methods of exonic and genomic analyses
  11. Chapter 10 Association, cause, and causal association. Revision 2: playing the changes
  12. Chapter 11 Adeno-associated virus-mediated gene therapy in central nervous system genetic disorders
  13. Chapter 12 Genomics of human neurological disorders
  14. Chapter 13 CRISPR/Cas9-based genetic engineering for translational research in neurological disorders
  15. Chapter 14 Neural cells derived from pluripotent stem cells and directly induced from somatic cells
  16. Chapter 15 Neuroimaging in dementia
  17. Chapter 16 Neuroethics
  18. Chapter 17 Genetic counseling
  19. Chapter 18 Antisense oligonucleotide drugs for neurological and neuromuscular diseases
  20. Chapter 19 Autophagy and neurological disorders
  21. Chapter 20 The aging brain
  22. Chapter 21 Cerebral malformations
  23. Chapter 22 Global developmental delay and intellectual disability
  24. Chapter 23 Aging and dementia in Down syndrome
  25. Chapter 24 An overview of Rett syndrome
  26. Chapter 25 Fragile X clinical features and neurobiology
  27. Chapter 26 Neurological evaluation and management of autism spectrum disorder
  28. Chapter 27 Angelman syndrome
  29. Chapter 28 The prion diseases
  30. Chapter 29 Leptin-related disorders of the nervous system
  31. Chapter 30 Genetics of autonomic disorders
  32. Chapter 31 The mitochondrial genome
  33. Chapter 32 Mitochondrial disorders due to mutations in the mitochondrial genome
  34. Chapter 33 Mitochondrial disorders due to mutations in the nuclear genome
  35. Chapter 34 Pyruvate dehydrogenase, pyruvate carboxylase, Krebs cycle, and mitochondrial transport disorders
  36. Chapter 35 Gaucher disease—neuronopathic forms
  37. Chapter 36 The Niemann–Pick diseases
  38. Chapter 37 GM2-gangliosidoses
  39. Chapter 38 Metachromatic leukodystrophy and multiple sulfatase deficiency
  40. Chapter 39 Krabbe disease: globoid cell leukodystrophy
  41. Chapter 40 Leukodystrophies—an overview
  42. Chapter 41 The mucopolysaccharidoses
  43. Chapter 42 The mucolipidoses
  44. Chapter 43 Disorders of glycoprotein degradation: α-mannosidosis, ÎČ-mannosidosis, fucosidosis, sialidosis, and aspartylglycosaminuria
  45. Chapter 44 GM1 gangliosidosis, Morquio disease, galactosialidosis, and sialidosis
  46. Chapter 45 Acid ceramidase deficiency: Farber lipogranulomatosis, spinal muscular atrophy associated with progressive myoclonic epilepsy and peripheral osteolysis
  47. Chapter 46 Wolman disease
  48. Chapter 47 Lysosomal membrane disorders: lysosome-associated membrane protein-2 deficiency (Danon disease)
  49. Chapter 48 Fabry disease: α-galactosidase A deficiency
  50. Chapter 49 Schindler disease: deficient α-N-acetylgalactosaminidase activity
  51. Chapter 50 Organic acid disorders
  52. Chapter 51 Glycogen and polyglucosan storage diseases
  53. Chapter 52 Disorders of galactose metabolism
  54. Chapter 53 Inborn errors of amino acid metabolism
  55. Chapter 54 Urea cycle disorders
  56. Chapter 55 Glucose transporter type I deficiency and other glucose flux disorders
  57. Chapter 56 Maple syrup urine disease: biochemical, clinical, and therapeutic considerations
  58. Chapter 57 Congenital disorders of N-linked Glycosylation
  59. Chapter 58 Disorders of glutathione metabolism
  60. Chapter 59 Canavan disease
  61. Chapter 60 Neurotransmitter disorders
  62. Chapter 61 Peroxisomal disorders
  63. Chapter 62 Purines and pyrimidines
  64. Chapter 63 The acute porphyrias
  65. Index