Mechanism and Genetic Susceptibility of Neurological Disorders
Mechanism and Genetic Susceptibility of Neurological Disorders
Khan, Andleeb; Rather, Mashoque Ahmad; Ashraf, Ghulam Md
Springer Verlag, Singapore
03/2024
417
Dura
Inglês
9789819994038
15 a 20 dias
Descrição não disponível.
Chapter 1. Neuropathology of neurological disorders.- Chapter 2. Head Trauma: Etiology, Pathophysiology, Clinical Manifestation and Biomarkers.- Chapter 3. Current Understanding of DNA Methylation in the Pathogenesis of Neuropathic Pain.- Chapter 4. Decoding dystrophin gene mutations: Unraveling the mysteries of muscular dystrophy.- Chapter 5. Etiology of Ataxia: A mechanistic insight of autoimmune, toxicity, and genetic approach.- Chapter 6. miRNA dysregulation in Schizophrenia.- Chapter 7. Muscular dystrophy: Underlying cellular & molecular mechanisms and various nanotherapeutic approaches for Muscular Dystrophy.- Chapter 8. Axonal degeneration, impaired axonal transport, and synaptic dysfunction in motor neuron disorder.- Chapter 9. Alterations in Receptor Genes in Huntington's disease.- Chapter 10. Genetic Modulators in Amyotrophic Lateral Sclerosis.- Chapter 11. Modulators and post-stroke behavioral changes.- Chapter 12. Presynaptic Dysfunction in Parkinson's Disease.- Chapter13. Mitochondrial Dysfunction and its Role in Neurological Disorders.- Chapter 14. Molecular and cellular mechanism of pathogen invasion into the Central nervous system: Meningitis.- Chapter 15. Muscular dystrophy: Mutations in the dystrophin gene.- Chapter 16. Gene editing tool for neurodegenerative diseases.- Chapter 17. Lumbar disc disease- an overview.
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Neurological diseases;Genetic susceptibility;Modulators in Neurological disorders;Metal Homeostasis;Therapeutic options
Chapter 1. Neuropathology of neurological disorders.- Chapter 2. Head Trauma: Etiology, Pathophysiology, Clinical Manifestation and Biomarkers.- Chapter 3. Current Understanding of DNA Methylation in the Pathogenesis of Neuropathic Pain.- Chapter 4. Decoding dystrophin gene mutations: Unraveling the mysteries of muscular dystrophy.- Chapter 5. Etiology of Ataxia: A mechanistic insight of autoimmune, toxicity, and genetic approach.- Chapter 6. miRNA dysregulation in Schizophrenia.- Chapter 7. Muscular dystrophy: Underlying cellular & molecular mechanisms and various nanotherapeutic approaches for Muscular Dystrophy.- Chapter 8. Axonal degeneration, impaired axonal transport, and synaptic dysfunction in motor neuron disorder.- Chapter 9. Alterations in Receptor Genes in Huntington's disease.- Chapter 10. Genetic Modulators in Amyotrophic Lateral Sclerosis.- Chapter 11. Modulators and post-stroke behavioral changes.- Chapter 12. Presynaptic Dysfunction in Parkinson's Disease.- Chapter13. Mitochondrial Dysfunction and its Role in Neurological Disorders.- Chapter 14. Molecular and cellular mechanism of pathogen invasion into the Central nervous system: Meningitis.- Chapter 15. Muscular dystrophy: Mutations in the dystrophin gene.- Chapter 16. Gene editing tool for neurodegenerative diseases.- Chapter 17. Lumbar disc disease- an overview.
?
?
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.