Page last updated: 2024-10-18

glycerol and Prader-Willi Syndrome

glycerol has been researched along with Prader-Willi Syndrome in 2 studies

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Prader-Willi Syndrome: An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229)

Research Excerpts

ExcerptRelevanceReference

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Höybye, C1
Hilding, A1
Marcus, C1
Thorén, M1
Bier, DM1
Kaplan, SL1
Havel, RJ1

Other Studies

2 other studies available for glycerol and Prader-Willi Syndrome

ArticleYear
Growth hormone induced lipolysis during short- and long-term administration in adult Prader-Willi patients.
    Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society, 2005, Volume: 15, Issue:6

    Topics: Adipose Tissue; Adult; Body Composition; Body Mass Index; Clinical Trials as Topic; Female; Genotype

2005
The Prader-Willi syndrome. Regulation of fat transport.
    Diabetes, 1977, Volume: 26, Issue:9

    Topics: Adipose Tissue; Adolescent; Adult; Biological Transport; Child; Diabetes Complications; Diabetes Mel

1977