Moyamoya Disease Update (PDF)
(Sprache: Englisch)
Moyamoya disease (MMD) was first reported as a new entity among vascular disorders in 1957. Named for the abnormal vascular networks found around the occluded distal internal carotid artery, it is the most common pediatric cerebrovascular disease in East...
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Moyamoya disease (MMD) was first reported as a new entity among vascular disorders in 1957. Named for the abnormal vascular networks found around the occluded distal internal carotid artery, it is the most common pediatric cerebrovascular disease in East Asia. In recent years large amounts of data on MMD have been collected and important investigations have been carried out in Japan and Korea, even as the pathophysiology of the disease remains to be discovered. This monograph covers a diversity of topics and presents a systematic compilation of the data and current status of MMD in clinical practice and basic research. With contributions by more than 70 authors, the book includes sections on genetics, computational analysis of hemodynamic shear stress, new imaging techniques, and endovascular treatment of MMD, along with practical applications and future directions for gene and stem cell therapies. For neurosurgeons as well as neurologists and pediatricians, this volume will help lead to more efficient and informed management of MMD.
Bibliographische Angaben
- Autoren: Byung-Kyu Cho , Teiji Tominaga
- 2010, 2010, 387 Seiten, Englisch
- Herausgegeben: Byung-Kyu Cho, Teiji Tominaga
- Verlag: Springer-Verlag GmbH
- ISBN-10: 4431997032
- ISBN-13: 9784431997030
- Erscheinungsdatum: 26.02.2010
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- Grösse: 12 MB
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Sprache:
Englisch
Pressezitat
From the reviews:“This is an almost 400-page book on the current status of all things relating to Moyamoya disease (MMD) definition, etiology, status of research, diagnostic modalities, and treatment options. … Illustrative of all this material … are well done, sharp, and clear, with good legends and explanatory material. … Certainly, this is the definitive book for someone who wishes information on Moyamoya disease. It is quite complete, almost excessively so, and will undoubtedly remain a basic source for several years to come.” (Robert M. Arensman, Doody’s Review Service, June, 2010)
“Moyamoya Disease Update, edited by Cho and Tominaga, provides an excellent update of this recent progress and a comprehensive overview of all relevant aspects of the disease. … This book is an exciting and highly recommended update on moyamoya disease. In addition to the scientific and clinical information, the book clearly indicates that recent years have been substantial progress in our understanding of the disease.” (Peter Vajkoczy, The Lancet Neurology, Vol. 9, August, 2010)
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