The newly updated Seventh Edition of the best-selling Manual of Neurologic Therapeutics is available in PDA format for instant access at the point of care. This easy-to-navigate handheld reference provides clear, current, clinically proven recommendations for diagnosis and treatment of neurologic disorders. Users can quickly find a disease by scrolling the table of contents or index and click on icons for specific information about the disease—description, diagnosis, prognosis, and treatment. A comprehensive, up-to-date neurology drug database provides complete information about specific drugs. Platform: Palm OS, Windows CE, and Pocket PC handheld devices Also Available for iPhone/IPod touch
A comprehensive and authoritative textbook, Neurological Therapeutics: Principles and Practice provides a reference that is both authoritative and accessible for daily use. The textbook explores the issues underlying treatment decisions not only for the most readily treated disorders but also for those conditions with few existing, definitive therapeutic options. With 600 figures, 37 in full color, tables, and a companion volume that is portable and easy-to-use, the final product is an important reference.
This is a practical book on neurological therapy. It is aimed at giving concise and updated answers to busy practicing clinicians in the clinic, ward, or emergency department. An evidence-based approach is used, but when there is no evidence or the data are inconclusive, an expert opinion is always given in order to meet the expectations of the reader. All neurological conditions, common and less common, are discussed; each chapter has a similar format, and contains an initial brief introduction on the epidemiology and clinical features of each disease. The therapy is then discussed, including pharmacological and non-pharmacological, with wide use of Tables & Figures. Flowcharts are also included in most of the chapters.
Neuronal Networks in Brain Function, CNS Disorders, and Therapeutics, edited by two leaders in the field, offers a current and complete review of what we know about neural networks. How the brain accomplishes many of its more complex tasks can only be understood via study of neuronal network control and network interactions. Large networks can undergo major functional changes, resulting in substantially different brain function and affecting everything from learning to the potential for epilepsy. With chapters authored by experts in each topic, this book advances the understanding of: - How the brain carries out important tasks via networks - How these networks interact in normal brain function - Major mechanisms that control network function - The interaction of the normal networks to produce more complex behaviors - How brain disorders can result from abnormal interactions - How therapy of disorders can be advanced through this network approach This book will benefit neuroscience researchers and graduate students with an interest in networks, as well as clinicians in neuroscience, pharmacology, and psychiatry dealing with neurobiological disorders. - Utilizes perspectives and tools from various neuroscience subdisciplines (cellular, systems, physiologic), making the volume broadly relevant - Chapters explore normal network function and control mechanisms, with an eye to improving therapies for brain disorders - Reflects predominant disciplinary shift from an anatomical to a functional perspective of the brain - Edited work with chapters authored by leaders in the field around the globe – the broadest, most expert coverage available
Key features of this evidence-based work include more than 275 major topics covering the vast patient mix primarily treated by adult and pediatric neurologists; the most current definitive medical citations; section editors who are all internationally recognized leaders in their fields; new chapters addressing the important issues of stem cell therapy, pharmacogenomics, palliative care, the management of the organ donor, metabolic myelopathy, superficial siderosis and attention deficit hyperactivity disorde; and over 600 comprehensive summary tables and informative figures, with the most recent supporting recommendations to guide treatment decisions for effective and efficient patient management in the busy clinic setting.
This book introduces the Neurological Training and Educating Technical System (NTETS), providing readers with a useful tool for the recovery of motor function after incurring CNS lesions. NTETS is based on the essential theories of Chinese medicine, central nervous system plasticity and motor function, using the six-step Chinese Daoyin technique to induce the CNS potency. This rehabilitation technique not only applies to acute stage patients who suffer from motor dysfunction caused by CNS lesions, but is also used for regaining motor function in long-term patients who have not experienced any improved motor function through the common rehabilitation methods of today. This informative book on NTETS is a beneficial supplement to modern rehabilitation medicine and serves as a valuable resource for rehabilitation doctors, nurses, graduate students in this field or employees working in neurology, neurosurgery, orthopaedics and geriatrics departments.
Mental, neurological, and substance use disorders are common, highly disabling, and associated with significant premature mortality. The impact of these disorders on the social and economic well-being of individuals, families, and societies is large, growing, and underestimated. Despite this burden, these disorders have been systematically neglected, particularly in low- and middle-income countries, with pitifully small contributions to scaling up cost-effective prevention and treatment strategies. Systematically compiling the substantial existing knowledge to address this inequity is the central goal of this volume. This evidence-base can help policy makers in resource-constrained settings as they prioritize programs and interventions to address these disorders.
Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable condition. This authoritative guide provides a clear overview of the latest current and experimental approaches to the treatment of DMD and examines the clinical, genetic, and pathophysiological aspects of the disease i
This book provides a cutting-edge review of polyglutamine disorders. It primarily focuses on two main aspects: (1) the mechanisms underlying the pathologies’ development and progression, and (2) the therapeutic strategies that are currently being explored to stop or delay disease progression. Polyglutamine (polyQ) disorders are a group of inherited neurodegenerative diseases with a fatal outcome that are caused by an abnormal expansion of a coding trinucleotide repeat (CAG), which is then translated in an abnormal protein with an elongated glutamine tract (Q). To date, nine polyQ disorders have been identified and described: dentatorubral-pallidoluysian atrophy (DRPLA); Huntington’s disease (HD); spinal–bulbar muscular atrophy (SBMA); and six spinocerebellar ataxias (SCA 1, 2, 3, 6, 7, and 17). The genetic basis of polyQ disorders is well established and described, and despite important advances that have opened up the possibility of generating genetic models of the disease, the mechanisms that cause neuronal degeneration are still largely unknown and there is currently no treatment available for these disorders. Further, it is believed that the different polyQ may share some mechanisms and pathways contributing to neurodegeneration and disease progression.
