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Edited by Andrew S. Feigin and Karen E. Anderson, this book provides a cutting-edge overview of Huntington disease, encompassing clinical care, research, and therapeutic advances. It serves as a valuable resource for both clinical and research specialists seeking to expand their knowledge base, as well as advanced students from various backgrounds including neurology, psychiatry, neuropsychology, and genetics.
Huntington Disease covers all major areas of clinical care and research, including neurological symptoms, behavioral and cognitive symptoms, brain imaging, and family dynamics and therapeutic alliances. It delves into the devastating nature of the disease, highlighting the importance of interdisciplinary collaboration and communication among researchers and clinicians.
The book extensively covers clinical trials, including design considerations for therapeutic studies. It emphasizes the need for innovative treatments and experimental therapeutics to address the complex needs of individuals affected by HD. Biomarkers are also discussed as crucial tools for monitoring disease progression and treatment efficacy.
Huntington Disease adopts an interdisciplinary approach, providing essential information for non-neurologists and facilitating understanding of the disease. This comprehensive resource encourages collaboration and knowledge sharing among professionals from various fields, ultimately aiming to improve patient care and accelerate research progress.
Featuring chapters edited by leading experts in the field from around the globe, this book offers the broadest expert coverage available. It presents a balanced view of the disease, incorporating diverse perspectives and experiences to create a truly international resource.
Huntington Disease is part of the Handbook of Clinical Neurology series (Book 144). Published by Elsevier in November 2017, it comprises 312 pages and is available in hardcover format. The ISBN-10 is 0128018933, and the ISBN-13 is 978-0128018934. The book measures 5.9 x 0.9 x 8.3 inches.
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