Tuberous Sclerosis Complex
3rd Edition
Published on 19. August 1999
Book
Hardback
368 pages
978-0-19-512210-7 (ISBN)
Description
The third edition of a classic work originally published by Lippincott Raven. Tuberous Sclerosis is a genetic disease characterized by lesions of the skin and central nervous system, seizures, and sometimes severe mental retardation. This revised edition will include biological analysis of underlying genetic causes.
Reviews / Votes
From the previous edition:'This book will clearly be of use to a wide variety of physicians who are involved ... with this bewildering disorder'Journal of Neuropathology and Experimental Neurology
More details
Series
Edition
3rd Revised edition
Language
English
Place of publication
New York
United States
Target group
Professional and scholarly
Edition type
Revised edition
Illustrations
3 colour plates, numerous halftones, 18 line drawings
Dimensions
Height: 236 mm
Width: 155 mm
Thickness: 25 mm
Weight
816 gr
ISBN-13
978-0-19-512210-7 (9780195122107)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Manuel R. Gomez | Julian R. Sampson | Vicky Holets Whittemore
Tuberous Sclerosis Complex
E-Book
12/1999
3rd Edition
Oxford University Press
€65.99
Available for download
Persons
Editor
Emeritus Professor of Pediatric NeurologyEmeritus Professor of Pediatric Neurology, Mayo Medical School, USA
Senior Lecturer in Medical GeneticsSenior Lecturer in Medical Genetics, University of Wales College of Medicine
Medical DirectorMedical Director, National Tuberous Sclerosis Association, USA
Content
Foreword ; Preface ; 1. History ; 2. Criteria for Diagnosis ; 3. Population Studies ; 4. Natural History of Cerebral TSC ; 5. Psychiatric Features ; 6. Electroencephalography ; 7. magnetoencephalography ; 8. Central Nervous System Imaging ; 9. Neuropathology ; 10. Ophthalmic Findings ; 11. Dermatologic Manifestions ; 12. Renal Involvement ; 13. Cardiac Manifestations ; 14. Pulmonary Manifestations ; 15. The Endocrine System ; 16. Liver, Dig Tract, Spleen, Arteries, Lymph ; 17. Imaging of Bone and Great Vessels ; 18. Lineagages of Cells in the CNS ; 19. Gene Mapping: TSC 1 ; 20. Mapping of TSC2: Tuberin ; 21. Genetic Counselling ; 22. Impact of Diagnosis on Patient and Family