Description |
1 online resource (xx, 387 pages) : illustrations (some color), portrait |
Contents |
Moyamoya Disease Update; Title Page; Copyright Page; Foreword; Preface; Contents; Contributors; Part I: Introduction; Part II: Epidemiology; Part III: Genetics; Part IV: Pathophysiology I: Protein, Cell, and Immunology; Part V: Pathophysiology II: Hemodynamics, Biomechanical Aspect; Part VI: Clinical Features; Part VII: Diagnostic Evaluation I: Morphological Imaging; Part VIII: Diagnostic Evaluation II: Functional Imaging; Part IX: Diagnostic Evaluation III: Electrophysiology; Part X: Surgical Technique; Part XI: Surgical Outcome; Part XII: Special Consideration I |
Summary |
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. This title compiles the data and status of MMD in clinical practice and basic research |
Bibliography |
Includes bibliographical references and index |
Notes |
Print version record |
In |
Springer eBooks |
Subject |
Moyamoya disease.
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Moyamoya Disease
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MEDICAL -- Neurology.
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Médecine.
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Moyamoya disease
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Form |
Electronic book
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Author |
Cho, Byung-Kyu
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Tominaga, Teiji
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LC no. |
2009943063 |
ISBN |
9784431997030 |
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4431997032 |
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