Results 131 to 140 of about 18,942 (235)
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
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
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
Vykat XR (diazoxide choline-extended release): a new FDA-approved treatment for hyperphagia in Prader-Willi syndrome. [PDF]
Pokhrel P +5 more
europepmc +1 more source
Assessing the impact of hyperphagia on the behaviour of children with Prader-Willi Syndrome
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
Clinical Improvements with Setmelanotide in a 2-Year-Old Patient with Hyperphagia and Obesity due to Leptin Receptor Deficiency: A Case Report. [PDF]
Pons MR +3 more
europepmc +1 more source
Protein-truncating variants in APBA1 in minors with severe, early-onset obesity: implications for genetic testing. [PDF]
Lerner J +10 more
europepmc +1 more source
Methylphenidate use in hyperphagic Prader-Willi syndrome: A clinical note. [PDF]
Saruhan K.
europepmc +1 more source
Mirtazepine causing hyperphagia [PDF]
R. T. Abed, M. Cooper
openaire +1 more source

