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