Cargando…

Hyperphagia and Obesity in Prader–Willi Syndrome: PCSK1 Deficiency and Beyond?

Prader–Willi syndrome (PWS) is a complex genetic disorder that, besides cognitive impairments, is characterized by hyperphagia, obesity, hypogonadism, and growth impairment. Proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency, a rare recessive congenital disorder, partially overlaps phe...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ramos-Molina, Bruno, Molina-Vega, María, Fernández-García, José C., Creemers, John W.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2018
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027271/ https://www.ncbi.nlm.nih.gov/pubmed/29880780 http://dx.doi.org/10.3390/genes9060288

Ejemplares similares

Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome
por: Polex-Wolf, Joseph, et al.
Publicado: (2018)

Medication Trials for Hyperphagia and Food-Related Behaviors in Prader–Willi Syndrome
por: Miller, Jennifer L., et al.
Publicado: (2015)

Development and validation of the Pediatric-Youth Hyperphagia Assessment for Prader-Willi syndrome
por: Cho, Sung Yoon, et al.
Publicado: (2022)

Hyperinsulinemia is a probable trigger for weight gain and hyperphagia in individuals with Prader‐Willi syndrome
por: Kweh, Frederick A., et al.
Publicado: (2023)

Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader–Willi syndrome
por: Davies, Jennifer R., et al.
Publicado: (2015)

Characteristics and relationship between hyperphagia, anxiety, behavioral challenges and caregiver burden in Prader-Willi syndrome
por: Kayadjanian, Nathalie, et al.
Publicado: (2021)

The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome
por: Licenziati, Maria Rosaria, et al.
Publicado: (2022)

Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial
por: Roof, Elizabeth, et al.
Publicado: (2023)

Prader-Willi Syndrome and Growth Hormone Deficiency
por: Aycan, Zehra, et al.
Publicado: (2014)

Analysis of Hyperphagia Questionnaire for Clinical Trials (HQ-CT) scores in typically developing individuals and those with Prader-Willi syndrome
por: Matesevac, Lisa, et al.
Publicado: (2023)

SUN-608 Juvenile Toxicity Study of Livoletide: A Peptide Analogue of Unacylated Ghrelin for the Treatment of Hyperphagia in Prader-Willi Syndrome
por: Xu, Howard, et al.
Publicado: (2020)

SUN-609 Livoletide (AZP-531), an Unacylated Ghrelin Analogue, Improves Hyperphagia and Food-Related Behaviors Both in Obese and Non-Obese People with Prader-Willi Syndrome
por: Harisseh, Rania, et al.
Publicado: (2020)

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

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

Prader-Willi Syndrome: Obesity due to Genomic Imprinting
por: Butler, Merlin G
Publicado: (2011)

Obesity management in Prader–Willi syndrome: current perspectives
por: Crinò, Antonino, et al.
Publicado: (2018)

Prader-Willi syndrome: an update on obesity and endocrine problems
por: Kim, Su Jin, et al.
Publicado: (2021)

Intensive management of obesity in people with Prader-Willi syndrome
por: Nolan, Brendan J., et al.
Publicado: (2022)

MON-102 Nonclinical Development of AZP-531 (Livoletide): A Peptide Analog of Unacylated Ghrelin for the Treatment of Hyperphagia in Prader-Willi Syndrome
por: Milano, Stephane, et al.
Publicado: (2019)

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

Topline Results of the CARE-PWS Phase 3 Study: Intranasal Carbetocin Improves Hyperphagia and Anxiety and Distress Symptoms in Prader-Willi Syndrome (PWS)
por: Ryman, Davis, et al.
Publicado: (2021)

Prader-Willi Syndrome: Clinical Aspects
por: Elena, Grechi, et al.
Publicado: (2012)

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

Approach to the Patient With Prader–Willi Syndrome
por: Höybye, Charlotte, et al.
Publicado: (2022)

Sleep Consequences of Prader-Willi Syndrome
por: Itani, Reem, et al.
Publicado: (2023)

Causes of Death in Prader-Willi Syndrome: Prader-Willi Syndrome Association (USA) 40-Year Mortality Survey
por: Butler, Merlin G., et al.
Publicado: (2016)

Prader–Willi Syndrome with Angelman Syndrome in the Offspring
por: Greco, Donatella, et al.
Publicado: (2021)

Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
por: Heseding, Hannah M., et al.
Publicado: (2022)

Nutritional intakes in children with Prader–Willi syndrome and non-congenital obesity
por: Rubin, Daniela A., et al.
Publicado: (2015)

Obesity in Prader–Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches
por: Muscogiuri, G., et al.
Publicado: (2021)

Alteration of brain nuclei in obese children with and without Prader-Willi syndrome
por: Wu, Ning, et al.
Publicado: (2022)

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

Prader-Willi syndrome: A primer for clinicians
por: Cataletto, Mary, et al.
Publicado: (2011)

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

Clinical and laboratory characteristics of Prader-Willi syndrome
por: Thao, Bui Phuong, et al.
Publicado: (2013)

Gall bladder agenesis in Prader Willi syndrome
por: Nair, Abilash, et al.
Publicado: (2015)

Adult Prader-Willi Syndrome: An Update on Management
por: Ho-Ming, Luk
Publicado: (2016)

Pituitary-Adrenal Axis in Prader Willi Syndrome
por: Edgar, Olivia S., et al.
Publicado: (2016)

Dietary Management for Adolescents with Prader–Willi Syndrome
por: Miller, Jennifer L, et al.
Publicado: (2020)

Pharmacodynamic Gene Testing in Prader-Willi Syndrome
por: Forster, Janice, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_su686u595510kv1j62q9vf5bbi