Page last updated: 2024-08-23

s-adenosylmethionine and Labhart-Willi Syndrome

s-adenosylmethionine has been researched along with Labhart-Willi Syndrome in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Driscoll, DJ; Lynn, CH; Miller, JL; Shuster, J1
Liu, Y; Ma, Y; Song, F; Song, J; Wang, Q; Wu, T; Yang, Y1

Other Studies

2 other study(ies) available for s-adenosylmethionine and Labhart-Willi Syndrome

ArticleYear
Carnitine and coenzyme Q10 levels in individuals with Prader-Willi syndrome.
    American journal of medical genetics. Part A, 2011, Volume: 155A, Issue:3

    Topics: Carnitine; Case-Control Studies; Child; Female; Humans; Male; Prader-Willi Syndrome; Siblings; Ubiquinone

2011
Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy.
    Journal of pediatric endocrinology & metabolism : JPEM, 2012, Volume: 25, Issue:11-12

    Topics: Arginine; Carboxylic Acids; Carnitine; Chromosomes, Human, Pair 15; Diet Therapy; Early Diagnosis; Failure to Thrive; Female; Gene Deletion; Humans; In Situ Hybridization, Fluorescence; Infant; Infant Nutrition Disorders; Infant, Newborn; Male; Prader-Willi Syndrome; Time-to-Treatment

2012