Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.

Prader-Willi syndrome (PWS) is a complex disorder combining hypothalamic dysfunction, neurodevelopmental delay, hypotonia, and hyperphagia with risk of obesity and its complications. PWS is caused by the loss of expression of the PWS critical region, a cluster of paternally expressed genes on chromo...

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Autores: Pellikaan K, Nguyen NQC, Rosenberg AGW, Coupaye M, Goldstone AP, Høybye C, Markovic T, Grugni G, Crinò A, Caixàs A, Poitou C, Corripio R, Nieuwenhuize RM, van der Lely AJ, de Graaff LCG
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Recursos:Institut d'Investigació i Innovació Parc Taulí (I3PT)
Repositorio:r-I3PT. Repositorio Institucional Producción Científica del Institut d'Investigació i Innovació Parc Taulí
OAI Identifier:oai:i3pt.fundanetsuite.com:p4213
Acesso em linha:https://i3pt.portalinvestigacion.com/publicaciones/4213
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85177103492&doi=10.1210%2fclinem%2fdgad312&partnerID=40&md5=34c653dbfb6351415e1ed91ac716aebf
Access Level:acceso abierto
Palavra-chave:Prader-Willi syndrome, comorbidity, hypothalamo-hypophyseal system, neoplasms
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spelling Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.Pellikaan KNguyen NQCRosenberg AGWCoupaye MGoldstone APHøybye CMarkovic TGrugni GCrinò ACaixàs APoitou CCorripio RNieuwenhuize RMvan der Lely AJde Graaff LCGPrader-Willi syndrome, comorbidity, hypothalamo-hypophyseal system, neoplasmsPrader-Willi syndrome (PWS) is a complex disorder combining hypothalamic dysfunction, neurodevelopmental delay, hypotonia, and hyperphagia with risk of obesity and its complications. PWS is caused by the loss of expression of the PWS critical region, a cluster of paternally expressed genes on chromosome 15q11.2-q13. As life expectancy of patients with PWS increases, age-related diseases like malignancies might pose a new threat to health.ENDOCRINE SOC2023info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://i3pt.portalinvestigacion.com/publicaciones/4213https://www.scopus.com/inward/record.uri?eid=2-s2.0-85177103492&doi=10.1210%2fclinem%2fdgad312&partnerID=40&md5=34c653dbfb6351415e1ed91ac716aebfJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISMISSN: 0021972XISSNe: 19457197reponame:r-I3PT. Repositorio Institucional Producción Científica del Institut d'Investigació i Innovació Parc Taulíinstname:Institut d'Investigació i Innovació Parc Taulí (I3PT)Inglésinfo:eu-repo/semantics/openAccessoai:i3pt.fundanetsuite.com:p42132026-06-21T15:30:37Z
dc.title.none.fl_str_mv Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
title Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
spellingShingle Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
Pellikaan K
Prader-Willi syndrome, comorbidity, hypothalamo-hypophyseal system, neoplasms
title_short Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
title_full Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
title_fullStr Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
title_full_unstemmed Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
title_sort Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review.
dc.creator.none.fl_str_mv Pellikaan K
Nguyen NQC
Rosenberg AGW
Coupaye M
Goldstone AP
Høybye C
Markovic T
Grugni G
Crinò A
Caixàs A
Poitou C
Corripio R
Nieuwenhuize RM
van der Lely AJ
de Graaff LCG
author Pellikaan K
author_facet Pellikaan K
Nguyen NQC
Rosenberg AGW
Coupaye M
Goldstone AP
Høybye C
Markovic T
Grugni G
Crinò A
Caixàs A
Poitou C
Corripio R
Nieuwenhuize RM
van der Lely AJ
de Graaff LCG
author_role author
author2 Nguyen NQC
Rosenberg AGW
Coupaye M
Goldstone AP
Høybye C
Markovic T
Grugni G
Crinò A
Caixàs A
Poitou C
Corripio R
Nieuwenhuize RM
van der Lely AJ
de Graaff LCG
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Prader-Willi syndrome, comorbidity, hypothalamo-hypophyseal system, neoplasms
topic Prader-Willi syndrome, comorbidity, hypothalamo-hypophyseal system, neoplasms
description Prader-Willi syndrome (PWS) is a complex disorder combining hypothalamic dysfunction, neurodevelopmental delay, hypotonia, and hyperphagia with risk of obesity and its complications. PWS is caused by the loss of expression of the PWS critical region, a cluster of paternally expressed genes on chromosome 15q11.2-q13. As life expectancy of patients with PWS increases, age-related diseases like malignancies might pose a new threat to health.
publishDate 2023
dc.date.none.fl_str_mv 2023
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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dc.identifier.none.fl_str_mv https://i3pt.portalinvestigacion.com/publicaciones/4213
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85177103492&doi=10.1210%2fclinem%2fdgad312&partnerID=40&md5=34c653dbfb6351415e1ed91ac716aebf
url https://i3pt.portalinvestigacion.com/publicaciones/4213
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85177103492&doi=10.1210%2fclinem%2fdgad312&partnerID=40&md5=34c653dbfb6351415e1ed91ac716aebf
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv ENDOCRINE SOC
publisher.none.fl_str_mv ENDOCRINE SOC
dc.source.none.fl_str_mv JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
ISSN: 0021972X
ISSNe: 19457197
reponame:r-I3PT. Repositorio Institucional Producción Científica del Institut d'Investigació i Innovació Parc Taulí
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