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Tuberous Sclerosis Complex: From Basic Science to Clinical Phenotypes
Contributor(s): Curatolo, Paolo (Editor)
ISBN: 1898683395     ISBN-13: 9781898683391
Publisher: Mac Keith Press
OUR PRICE:   $71.25  
Product Type: Hardcover
Published: January 2003
Qty:
Annotation: "This is clearly the most authoritative and contemporary statement of current knowledge yet published."
from the Foreword by H. Sarnat

Tuberous sclerosis is the prototype of a category of malformations uniquely characterized by disturbances in cellular differentiation and growth. It presents with a complex association of different neurological phenotypes, including seizures, cognitive impairments and autism. It is important not only because it is a relatively common hereditary neurological disease with high morbidity, but because it has implications in other pathological processes, such as dysplasia and neoplasia, hamartoma formation and other disturbances in morphogenic processes.

This book correlates new genetic data and basic science, covers clinical presentation, reviews the historical background and current diagnostic criteria, and deals with the recent advances in neuropathology, molecular genetics and neurobiology which give a better understanding of the pathogenesis of the disease.

Paediatricians and child neurologists will find this book uniquely useful.


Additional Information
BISAC Categories:
- Medical | Pediatrics
- Medical | Neurology
Dewey: 616.8
LCCN: 2004445919
Series: International Review of Child Neurology
Physical Information: 1" H x 9.3" W x 6.4" (1.4 lbs) 328 pages
 
Descriptions, Reviews, Etc.
Publisher Description:
This is clearly the most authoritative and contemporary statement of current knowledge yet published.
from the Foreword by H. Sarnat

Tuberous sclerosis is the prototype of a category of malformations uniquely characterized by disturbances in cellular differentiation and growth. It presents with a complex association of different neurological phenotypes, including seizures, cognitive impairments and autism. It is important not only because it is a relatively common hereditary neurological disease with high morbidity, but because it has implications in other pathological processes, such as dysplasia and neoplasia, hamartoma formation and other disturbances in morphogenic processes.

This book correlates new genetic data and basic science, covers clinical presentation, reviews the historical background and current diagnostic criteria, and deals with the recent advances in neuropathology, molecular genetics and neurobiology which give a better understanding of the pathogenesis of the disease.

Paediatricians and child neurologists will find this book uniquely useful.


Contributor Bio(s): Curatolo, Paolo: - Professor of Pediatric Neurology and Psychiatry, Department of Neuroscience, University of Rome Tor Vergata; Head of the Section of Pediatric Neurology, University of Rome Tor Vergata.