Prader-Willi syndrome: development and manifestations
Prader-Willi syndrome (PWS) is associated with an assortment of physical, behavioural and cognitive abnormalities which create a broad range of care needs. Information about the syndrome is spread across a variety of disciplines. In this 2004 book the authors seek to identify and provide the latest...
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Format: | Elektronisch Tagungsbericht E-Book |
Sprache: | English |
Veröffentlicht: |
Cambridge
Cambridge University Press
2004
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Schlagworte: | |
Online-Zugang: | BSB01 FHN01 Volltext |
Zusammenfassung: | Prader-Willi syndrome (PWS) is associated with an assortment of physical, behavioural and cognitive abnormalities which create a broad range of care needs. Information about the syndrome is spread across a variety of disciplines. In this 2004 book the authors seek to identify and provide the latest findings about how best to manage the complex medical, nutritional, psychological, educational, social and therapeutic needs of people with PWS. Their approach is an integrated one, centred on the PWS phenotype. Both authors have been involved in the Cambridge PWS study, which is the largest and most rounded of the cohort studies of PWS anywhere in the world. The unique data it provides is the basis of this book |
Beschreibung: | Title from publisher's bibliographic system (viewed on 05 Oct 2015) |
Beschreibung: | 1 online resource (x, 220 pages) |
ISBN: | 9780511543869 |
DOI: | 10.1017/CBO9780511543869 |
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Datensatz im Suchindex
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any_adam_object | |
author | Whittington, Joyce |
author_facet | Whittington, Joyce |
author_role | aut |
author_sort | Whittington, Joyce |
author_variant | j w jw |
building | Verbundindex |
bvnumber | BV043945741 |
collection | ZDB-20-CBO |
contents | Background and historical overview -- Biological and regulatory mechanisms in PWS -- The Cambridge PWS project -- Prevalence, birth incidence and mortality -- Relationship between genetic and clinical diagnosis -- Phenotypic differences between the genetic subtypes -- Cognitive function and attainments -- The behavioural phenotype of PWS -- Medical conditions affecting people with PWS -- Psychiatric illness -- Obsessions and compulsions -- Understanding PWS. |
ctrlnum | (ZDB-20-CBO)CR9780511543869 (OCoLC)850829765 (DE-599)BVBBV043945741 |
dewey-full | 618.92/85884 |
dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 618 - Gynecology, obstetrics, pediatrics, geriatrics |
dewey-raw | 618.92/85884 |
dewey-search | 618.92/85884 |
dewey-sort | 3618.92 585884 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
doi_str_mv | 10.1017/CBO9780511543869 |
format | Electronic Conference Proceeding eBook |
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id | DE-604.BV043945741 |
illustrated | Not Illustrated |
indexdate | 2024-07-10T07:39:24Z |
institution | BVB |
isbn | 9780511543869 |
language | English |
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publishDate | 2004 |
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publisher | Cambridge University Press |
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spelling | Whittington, Joyce Verfasser aut Prader-Willi syndrome development and manifestations Joyce Whittington and Tony Holland Cambridge Cambridge University Press 2004 1 online resource (x, 220 pages) txt rdacontent c rdamedia cr rdacarrier Title from publisher's bibliographic system (viewed on 05 Oct 2015) Background and historical overview -- Biological and regulatory mechanisms in PWS -- The Cambridge PWS project -- Prevalence, birth incidence and mortality -- Relationship between genetic and clinical diagnosis -- Phenotypic differences between the genetic subtypes -- Cognitive function and attainments -- The behavioural phenotype of PWS -- Medical conditions affecting people with PWS -- Psychiatric illness -- Obsessions and compulsions -- Understanding PWS. Prader-Willi syndrome (PWS) is associated with an assortment of physical, behavioural and cognitive abnormalities which create a broad range of care needs. Information about the syndrome is spread across a variety of disciplines. In this 2004 book the authors seek to identify and provide the latest findings about how best to manage the complex medical, nutritional, psychological, educational, social and therapeutic needs of people with PWS. Their approach is an integrated one, centred on the PWS phenotype. Both authors have been involved in the Cambridge PWS study, which is the largest and most rounded of the cohort studies of PWS anywhere in the world. The unique data it provides is the basis of this book Prader-Willi syndrome Holland, Tony 1948- Sonstige oth Prader-Willi Syndrome Association issuing body Sonstige oth Erscheint auch als Druckausgabe 978-0-521-17337-7 Erscheint auch als Druckausgabe 978-0-521-84029-3 https://doi.org/10.1017/CBO9780511543869 Verlag URL des Erstveröffentlichers Volltext |
spellingShingle | Whittington, Joyce Prader-Willi syndrome development and manifestations Background and historical overview -- Biological and regulatory mechanisms in PWS -- The Cambridge PWS project -- Prevalence, birth incidence and mortality -- Relationship between genetic and clinical diagnosis -- Phenotypic differences between the genetic subtypes -- Cognitive function and attainments -- The behavioural phenotype of PWS -- Medical conditions affecting people with PWS -- Psychiatric illness -- Obsessions and compulsions -- Understanding PWS. Prader-Willi syndrome |
title | Prader-Willi syndrome development and manifestations |
title_auth | Prader-Willi syndrome development and manifestations |
title_exact_search | Prader-Willi syndrome development and manifestations |
title_full | Prader-Willi syndrome development and manifestations Joyce Whittington and Tony Holland |
title_fullStr | Prader-Willi syndrome development and manifestations Joyce Whittington and Tony Holland |
title_full_unstemmed | Prader-Willi syndrome development and manifestations Joyce Whittington and Tony Holland |
title_short | Prader-Willi syndrome |
title_sort | prader willi syndrome development and manifestations |
title_sub | development and manifestations |
topic | Prader-Willi syndrome |
topic_facet | Prader-Willi syndrome |
url | https://doi.org/10.1017/CBO9780511543869 |
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