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Amyotrophic Lateral Sclerosis: From Diagnosis to Treatment focuses on two aspects of neuroimaging related to amyotrophic lateral sclerosis that have greatly evolved in the last decades: the development of optical tools in the biology field and advances in the field of magnetic resonance imaging. Therapeutic writing and expressive disclosure interventions have been demonstrated to facilitate the emotional processing of thoughts and feelings about the amyotrophic lateral sclerosis experience, with relevant implications for illness adjustment. Based on these premises, the authors explore the linguistic patterns in the cognitive-affective processing of illness experience in people with amyotrophic lateral sclerosis. Following this, the authors discuss recent studies that offer a new perspective on sensory networks in motor neuron diseases to understand the true extent and patophysiology of amyotrophic lateral sclerosis and suggest new potential biomarkers for the diagnosis of this tragic disease. The closing study focuses on the respiratory involvement of amyotrophic lateral sclerosis, which is the principal cause of death. Amyotrophic lateral sclerosis is characterized by respiratory failure consequent to respiratory muscles dysfunction, as well as bulbar muscles which support the upper airways, developing in dyspnoea and impaired sleep.

The Molecular and Clinical Pathology of Neurodegenerative Disease brings together in one volume our current understanding of the molecular basis of neurodegeneration in humans, targeted at neuroscientists and graduate students in neuroscience, and the biomedical and biological sciences. Bringing together up-to-date molecular biology data with clinical evidence, this book sheds a light on common molecular mechanisms that underlie many different neurodegenerative diseases and addresses the molecular pathologies in each. The combined research and clinical background of the authors provides a unique perspective in relating clinical experiences with the molecular understanding needed to examine these diseases and is a must-read for anyone who wants to learn more about neurodegeneration. - Provides an up-to-date summary of neurodegeneration at a molecular, cellular, and tissue level for the most common human disorders - Describes the clinical background and underlying molecular processes for Alzheimer's disease, Parkinson's, Prion, Motor Neuron, Huntington's, and Multiple Sclerosis - Highlights the state-of-the-art treatment options for each disorder - Details examples of relevant cutting edge experimental systems, including genome editing and human pluripotent stem cell-derived neuronal models