Huntington’s Disease 1st Edition

Huntington’s Disease, 1st Edition by Xiangdong William Yang, Myriam Heiman, and Leslie M. Thompson is an essential, authoritative resource for clinicians, researchers, students, and families confronting this complex neurodegenerative disorder. Combining rigorous science with practical clinical insight, this first edition synthesizes current knowledge on genetics, pathogenesis, diagnosis, and care — making it indispensable for those working in neurology, psychiatry, genetic counseling, and translational research.

Beginning with clear explanations of the HTT gene mutation and molecular mechanisms, the book guides readers through phenotype variability, progression markers, and state-of-the-art diagnostic approaches. Detailed chapters explore symptomatic and supportive management, multidisciplinary care models, and evolving therapeutic strategies, including gene-targeted and neuroprotective approaches. Ethical, psychosocial, and caregiving considerations are addressed with compassion and evidence-based guidance, making the text useful not only to professionals but also to families seeking trusted information.

Designed for a global audience, the content is relevant to practitioners and institutions across North America, Europe, Asia, and beyond, supporting clinical decision-making and research collaboration worldwide. With extensive references and clear clinical takeaways, this volume bridges bench-to-bedside translation and frames future directions in Huntington’s Disease research and care.

Whether you’re updating clinical practice, designing research, or caring for a loved one, Huntington’s Disease, 1st Edition offers clarity, depth, and practical value. Order now to bring leading expertise into your library and stay at the forefront of Huntington’s Disease knowledge.

Note: eBooks do not include supplementary materials such as CDs, access codes, etc.