Cargando…

Effect of cessation of GH treatment on cognition during transition phase in Prader-Willi syndrome: results of a 2-year crossover GH trial

BACKGROUND: Patients with Prader-Willi syndrome (PWS) have a cognitive impairment. Growth hormone (GH) treatment during childhood improves cognitive functioning, while cognition deteriorates in GH-untreated children with PWS. Cessation of GH treatment at attainment of adult height (AH) might deterio...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kuppens, R. J., Mahabier, E. F., Bakker, N. E., Siemensma, E. P. C., Donze, S. H., Hokken-Koelega, A. C. S.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112648/ https://www.ncbi.nlm.nih.gov/pubmed/27852283 http://dx.doi.org/10.1186/s13023-016-0535-7

Ejemplares similares

Prevalence of growth hormone (GH) deficiency in previously GH‐treated young adults with Prader‐Willi syndrome
por: Donze, Stephany H., et al.
Publicado: (2019)

Three years of growth hormone treatment in young adults with Prader-Willi syndrome: sustained positive effects on body composition
por: Damen, Layla, et al.
Publicado: (2020)

Twenty Years of GH Treatment in Adults with Prader-Willi Syndrome
por: Sjöström, Anna, et al.
Publicado: (2021)

Growth Hormone (GH) Treatment Decreases Plasma Kisspeptin Levels in GH-Deficient Adults with Prader–Willi Syndrome
por: Giménez-Palop, Olga, et al.
Publicado: (2021)

Evidence for Accelerated Biological Aging in Young Adults with Prader–Willi Syndrome
por: Donze, Stephany H, et al.
Publicado: (2019)

Elevated ratio of acylated to unacylated ghrelin in children and young adults with Prader–Willi syndrome
por: Kuppens, R. J., et al.
Publicado: (2015)

Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
por: Damen, Layla, et al.
Publicado: (2020)

SAT-446 No Central Adrenal Insufficiency Found in Adults with Prader-Willi Syndrome Tested by Multiple-Dose Metyrapone Test
por: Davidse, Kirsten, et al.
Publicado: (2019)

Reduced Cortical Complexity in Children with Prader-Willi Syndrome and Its Association with Cognitive Impairment and Developmental Delay
por: Lukoshe, Akvile, et al.
Publicado: (2014)

Prenatal and Neonatal Characteristics of Children with Prader-Willi Syndrome
por: Grootjen, Lionne N., et al.
Publicado: (2022)

Atypical 15q11.2-q13 Deletions and the Prader-Willi Phenotype
por: Grootjen, Lionne N., et al.
Publicado: (2022)

Long-term effects of GH therapy in adult patients with Prader-Willi syndrome: a longitudinal study
por: Grugni, Graziano, et al.
Publicado: (2023)

Appetite- and weight-inducing and -inhibiting neuroendocrine factors in Prader–Willi syndrome, Bardet–Biedl syndrome and craniopharyngioma versus anorexia nervosa
por: Vlaardingerbroek, H, et al.
Publicado: (2021)

High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome
por: Beauloye, Veronique, et al.
Publicado: (2016)

Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome
por: Lukoshe, Akvile, et al.
Publicado: (2013)

A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome
por: Bochukova, Elena G., et al.
Publicado: (2018)

Liraglutide for Weight Management in Children and Adolescents With Prader–Willi Syndrome and Obesity
por: Diene, Gwenaëlle, et al.
Publicado: (2022)

Altered functional resting-state hypothalamic connectivity and abnormal pituitary morphology in children with Prader-Willi syndrome
por: Lukoshe, Akvile, et al.
Publicado: (2017)

Acute stress response of the HPA-axis in children with Prader-Willi syndrome: new insights and consequences for clinical practice
por: Grootjen, Lionne N., et al.
Publicado: (2023)

Response to GH Treatment After Radiation Therapy Depends on Location of Irradiation
por: Rose, Susan R, et al.
Publicado: (2020)

Computer-aided facial analysis as a tool to identify patients with Silver–Russell syndrome and Prader–Willi syndrome
por: Ciancia, Silvia, et al.
Publicado: (2023)

GH safety workshop position paper: a critical appraisal of recombinant human GH therapy in children and adults
por: Allen, D B, et al.
Publicado: (2015)

Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome
por: Bingeliene, Arina, et al.
Publicado: (2015)

Regulation of GH and GH Signaling by Nutrients
por: Caputo, Marina, et al.
Publicado: (2021)

Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome
por: Pellikaan, Karlijn, et al.
Publicado: (2021)

Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
por: Cheon, Chong Kun
Publicado: (2016)

The GH/IGF-I axis in children with a meningococcal septic shock: striking differences between survivors and non-survivors
por: de Groof, F, et al.
Publicado: (2000)

Epigenetics in Prader-Willi Syndrome
por: Mendiola, Aron Judd P., et al.
Publicado: (2021)

Impact of transitional care on endocrine and anthropometric parameters in Prader–Willi syndrome
por: Paepegaey, A C, et al.
Publicado: (2018)

The transition from pediatric to adult care in individuals with Prader-Willi syndrome
por: Poitou, Christine, et al.
Publicado: (2022)

Is GH Replacement for Adult GH Deficiency Safe?
por: Melmed, Shlomo
Publicado: (2022)

GH deficiency status combined with GH receptor polymorphism affects response to GH in children
por: Valsesia, Armand, et al.
Publicado: (2015)

Endocrine manifestations and management of Prader-Willi syndrome
por: Emerick, Jill E, et al.
Publicado: (2013)

Hyperprolactinemia in Adults with Prader-Willi Syndrome
por: Sjöström, Anna, et al.
Publicado: (2021)

Special Issue: Genetics of Prader–Willi Syndrome
por: Godler, David E., et al.
Publicado: (2021)

Immobilization of Glycoside Hydrolase Families GH1, GH13, and GH70: State of the Art and Perspectives
por: Graebin, Natália G., et al.
Publicado: (2016)

Good cognitive performances in a child with Prader-Willi syndrome
por: Nugnes, Rosa, et al.
Publicado: (2013)

Genome-wide identification of GhAAI genes reveals that GhAAI66 triggers a phase transition to induce early flowering
por: Qanmber, Ghulam, et al.
Publicado: (2019)

Diagnosis of GH Deficiency Without GH Stimulation Tests
por: Ibba, Anastasia, et al.
Publicado: (2022)

Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry
por: Bohonowych, Jessica E., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_b5vcgradkqrqn01rokjf8loet1