Wilson Disease, Volume 142 (Handbook of Clinical Neurology)

by Anna Czlonkowska (Editor),‎ Michael Schilsky (Editor)

Wilson Disease is a genetic disorder that affects the liver and neurologic/psychiatric health. It is a disease of increasing interest to neurologists, hepatologists, and geneticists. If diagnosed early, it is treatable, and patients can live normal lives. The book “Wilson Disease” edited by Anna Czlonkowska and Michael Schilsky provides a comprehensive guide on this inherited genetic disorder. The book has extensive coverage of both diagnosis and medical and surgical approaches to treatment. It includes perspectives on both adult and pediatric diagnosis and treatment and a section on genetics highlighting advances in molecular diagnostics.

The book “Wilson Disease” provides a detailed description of the molecular pathophysiology of the disease and the clinical and pathological effects of copper. The book also describes the medical and surgical approaches to the treatment of the disease. It offers insights on both adult and pediatric diagnosis and treatment.

The book “Wilson Disease” is edited by Anna Czlonkowska and Michael Schilsky and authored by leaders in the field from around the globe. The book offers the widest, most expert coverage available on the topic.

The book “Wilson Disease” addresses the genetic disorder’s molecular pathophysiology, highlighting the clinical and pathological effects of copper. The editors and authors discuss and present different diagnosis and treatment approaches for both adult and pediatric patients. The book is published by Elsevier and available in digital format.

The book “Wilson Disease” provides a comprehensive understanding of the disease and its treatment approaches. The book’s structure is clear, concise, and well-organized, providing a unique learning experience for every reader. The book provides in-depth knowledge of the genetics behind the disease, including the molecular pathophysiology of the disease.

The book “Wilson Disease” provides a thorough analysis of the disease’s symptoms, diagnostic tests, and different treatment options. The book presents complex information in a simple, easy-to-read language and ensures that the reader grasps every concept and idea.

The book “Wilson Disease” is an essential read for anyone interested in understanding the genetic disease’s ins and outs, including clinicians and medical practitioners and students. This handbook is also important for patients and their families who want to learn more about their condition’s diagnosis and treatment.

Finally, the book “Wilson Disease” provides an in-depth look at the patient support groups and animal models available to aid in the disease’s treatment and research.

In conclusion, “Wilson Disease” edited by Anna Czlonkowska and Michael Schilsky is a comprehensive guide on Wilson Disease. It is an excellent resource for anyone interested in diagnosing, treating, and researching the disease. Its authors’ expertise, combined with its broad coverage of the topic, makes it an essential addition to any academic, health care, or personal library. Order your copy today to gain valuable insights and knowledge on Wilson Disease.

Product Details

• Addresses the molecular pathophysiology of WD and the clinical and pathological effects of copper
• Offers coverage of both diagnosis and medical and surgical approaches to treatment
• Includes perspectives on both adult and pediatric diagnosis and treatment
• Edited work with chapters authored by leaders in the field from around the globe―the broadest, most expert coverage available

• Series: Handbook of Clinical Neurology (Book 142)
• Hardcover: 264 pages
• Publisher: Elsevier; 1 edition (May 24, 2017)
• Language: English
• ISBN-10: 0444636250
• ISBN-13: 978-0444636256
• Product Dimensions: 7.5 x 0.8 x 10.2 inches