Rett Syndrome

Among the vast body of literature that has grown around Rett syndrome, this volume is the first to be aimed at both clinicians and researchers. It presents a comprehensive overview of the disorder and examines the areas where gaps in knowledge are most significant. Rett Syndrome is intended to be a guide for both initial examination and in-depth study of the disorder. It is a practical text for the physician approaching the disorder for the first time and a valuable reference resource for the specialist or researcher.

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Rett Syndrome

Among the vast body of literature that has grown around Rett syndrome, this volume is the first to be aimed at both clinicians and researchers. It presents a comprehensive overview of the disorder and examines the areas where gaps in knowledge are most significant. Rett Syndrome is intended to be a guide for both initial examination and in-depth study of the disorder. It is a practical text for the physician approaching the disorder for the first time and a valuable reference resource for the specialist or researcher.

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Overview

Among the vast body of literature that has grown around Rett syndrome, this volume is the first to be aimed at both clinicians and researchers. It presents a comprehensive overview of the disorder and examines the areas where gaps in knowledge are most significant. Rett Syndrome is intended to be a guide for both initial examination and in-depth study of the disorder. It is a practical text for the physician approaching the disorder for the first time and a valuable reference resource for the specialist or researcher.


Product Details

ISBN-13: 9781909962859
Publisher: MacKeith Press
Publication date: 09/23/2017
Series: Clinics in Developmental Medicine
Sold by: Barnes & Noble
Format: eBook
Pages: 225
File size: 5 MB

About the Author

Walter Kaufmann is Director of the Center for Translational Research and Curry Chair in Genetic Therapeutics at the Greenwood Genetic Center, South Carolina, USA. He is a clinician and researcher whose career has focused on characterizing the neurobehavioral phenotypes and underlying mechanisms of genetic disorders associated with intellectual disability and autism. His focus is the development of novel therapies for these disorders, including outcome measures and biomarkers for the corresponding clinical trials. Dr Kaufmann has carried out most of this work at the Kennedy Krieger Institute and Harvard Medical School (Boston Children’s Hospital) USA.
Alan Percy is a Professor in Child Neurology and currently the Interim Director of Clinical Neuroscience at the Civitan International Research Center, University of Alabama School of Medicine, Birmingham , USA. He trained in paediatrics at Stanford University Hospital and specialised in paediatric neurology at the Johns Hopkins University School of Medicine. Rett syndrome is his main interest. He has authored over 250 monographs, book chapters and journal articles. He is co-editor of the journal Translational Science of Rare Diseases and is on the Advisory Board of Rettsyndrome.org.
Angus Clarke is Professor and Honorary Consultant in Clinical Genetics at the Institute of Medical Genetics, University Hospital of Wales, UK. He established the Cardiff University MSc course in Genetic Counselling in 2000 and has been Course Director since then. Professor Clarke has particular interest in Rett syndrome and ectodermal dysplasia, the genetic counselling process and the social and ethical issues around human genetics. He has authored or edited seven books and numerous research papers and book chapters. His is also medical advisor to Rett UK.
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