Results 151 to 160 of about 26,081 (268)

Antisense Mapping of the MOR-1 Opioid Receptor Clone: Modulation of Hyperphagia Induced by DAMGO 1 [PDF]

, 2020
The mu opioid receptor mediates ingestive behavior: muselective agonists stimulate food intake and antagonists reduce intake in many ingestive situations.
Liza Leventhal, Richard J Bodnar, Lesley B Stevens, Grace C Rossi, Gavril W Pasternak   +4 more
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Prader-Willi Syndrome and the Role of Ghrelin in the Development of Hyperphagia : -A Literature Review [PDF]

Abstrakt Bakgrund: Prader Willis syndrom (PWS) är ett sällsynt syndrom som orsakas av en avvikelse på kromosom 15. Individer med PWS genomgår en övergång från ett anorektiskt stadie under första levnadsåret till att senare drabbas av en överdriven ...
Wengelin, Marlene
core   +4 more sources

The treatment of hyperphagia and obesity in Prader-Willi Syndrome [PDF]

Introduction: Prader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder, in which the central clinical characteristics are hyperphagia and obesity.
Jastrzębska, Ilona, Bilecki, Krzysztof, Nowoświat, Patrycja, Gugulski, Hubert, Bado, Michał, Kozicz, Michał Andrzej, Cuper, Paulina   +6 more
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Semaglutide in Adolescents Living With Obesity: A Real‐World Data Study Exploring Predictors of Treatment Response

Diabetes, Obesity and Metabolism, Volume 28, Issue 8, Page 7616-7621, August 2026.
Valeria Cimador, Sophie Robertson, Christine Desmond, Jessica Dodgson, Elizabeth van Boxel, Nikki L. Davis, Rebecca J. Moon   +6 more
wiley   +1 more source

Assessing the impact of hyperphagia on the behaviour of children with Prader-Willi Syndrome [PDF]

Background Prader-Willi Syndrome (PWS) is a complex genetic syndrome associated with hyperphagia and behavioural problems. Recent research suggested a link between hyperphagia and behavioural and emotional problems in PWS such as anger and anxiety ...
Haselip, L.
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Managing Hyperphagia, Obesity, and Hyperglycemia in Prader-Willi Syndrome: A Meta-Analysis of GLP-1 Agonists and SGLT2 Inhibitors

International Journal of Medical Students
Background: Prader-Willi Syndrome (PWS) is a genetic disorder caused by a deletion, mutation, or imprinting error of the paternal 15q11-13 region or by maternal uniparental disomy of chromosome 15.
Saumika Mulluri
doaj   +1 more source

Hyperphagia [PDF]

, 2020
openaire   +1 more source

Neuroendocrinology of hyperphagias and obesities [PDF]

Reproduction Nutrition Développement, 1980
openaire   +3 more sources

Kleine-Levin Syndorme: aetiology and pathogenesis, symptoms, diagnosis and treatment

Journal of Education, Health and Sport, 2018
AIM: The aim of the study is to present the aetiology, pathogenesis, symptoms, diagnosis and treatment of Kleine-Levin syndrome (KLS). VIEW: Kleine-Levin syndrome is an extremely rare disease entity that consists of attacks of hypersomnia, cognitive and
Kamila Tuzim, Tomasz Tuzim, Magdalena Urbańczuk, Marcin Urbańczuk, Katarzyna Schab   +4 more
doaj  

An Assessment of Obesity and Hyperphagia In Individuals With Smith-Magenis Syndrome [PDF]

, 2010
Smith-Magenis syndrome (SMS;OMIM# 182290) is a multiple congenital anomalies and mental retardation syndrome caused by a 3.7- Mb deletion on chromosome 17p11.2 or a mutation in the RAI1 gene.
Crain, Carrie A
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