Results 131 to 140 of about 18,942 (235)

Behavioral changes in patients with Prader-Willi syndrome receiving diazoxide choline extended-release tablets compared to the PATH for PWS natural history study

open access: yesJournal of Neurodevelopmental Disorders
Background Prader-Willi syndrome (PWS) is a rare neurobehavioral-metabolic disease caused by the lack of paternally expressed genes in the chromosome 15q11-q13 region, characterized by hypotonia, neurocognitive problems, behavioral difficulties ...
Theresa V. Strong   +11 more
doaj   +1 more source

Prader-Willi Syndrome and the Role of Ghrelin in the Development of Hyperphagia : -A Literature Review

open access: yes
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   +2 more sources

The treatment of hyperphagia and obesity in Prader-Willi Syndrome

open access: yes
Introduction: Prader-Willi Syndrome (PWS) is a genetic neurodevelopmental disorder, in which the central clinical characteristics are hyperphagia and obesity.
Jastrzębska, Ilona   +6 more
core  

Hypothalamic obesity. [PDF]

open access: yesRev Endocr Metab Disord
Farooqi IS, O'Rahilly S.
europepmc   +1 more source

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

open access: yes
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.
core  

Protein-truncating variants in APBA1 in minors with severe, early-onset obesity: implications for genetic testing. [PDF]

open access: yesMol Cell Pediatr
Lerner J   +10 more
europepmc   +1 more source

Mirtazepine causing hyperphagia [PDF]

open access: yesBritish Journal of Psychiatry, 1999
R. T. Abed, M. Cooper
openaire   +1 more source

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