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GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.
Deal CL, Tony M, Höybye C, Allen DB, Tauber M, Christiansen JS; 2011 Growth Hormone in Prader-Willi Syndrome Clinical Care Guidelines Workshop Participants. Deal CL, et al. J Clin Endocrinol Metab. 2013 Jun;98(6):E1072-87. doi: 10.1210/jc.2012-3888. Epub 2013 Mar 29. J Clin Endocrinol Metab. 2013. PMID: 23543664 Free PMC article. Review.
CONTEXT: Recombinant human GH (rhGH) therapy in Prader-Willi syndrome (PWS) has been used by the medical community and advocated by parental support groups since its approval in the United States in 2000 and in Europe in 2001. ...
CONTEXT: Recombinant human GH (rhGH) therapy in Prader-Willi syndrome (PWS) has been used by the medical community and …
Neuromodulation for the treatment of Prader-Willi syndrome - A systematic review.
Qiu L, Chang A, Ma R, Strong TV, Okun MS, Foote KD, Wexler A, Gunduz A, Miller JL, Halpern CH. Qiu L, et al. Neurotherapeutics. 2024 Apr;21(3):e00339. doi: 10.1016/j.neurot.2024.e00339. Epub 2024 Mar 2. Neurotherapeutics. 2024. PMID: 38430811 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a complex, genetic disorder characterized by multisystem involvement, including hyperphagia, maladaptive behaviors and endocrinological derangements. ...
Prader-Willi syndrome (PWS) is a complex, genetic disorder characterized by multisystem involvement, including hyperpha …
Physical exercise and Prader-Willi syndrome: A systematic review.
Morales JS, Valenzuela PL, Pareja-Galeano H, Rincón-Castanedo C, Rubin DA, Lucia A. Morales JS, et al. Clin Endocrinol (Oxf). 2019 May;90(5):649-661. doi: 10.1111/cen.13953. Epub 2019 Mar 18. Clin Endocrinol (Oxf). 2019. PMID: 30788853
OBJECTIVE: The aim of this systematic review was to summarize evidence on the acute responses of individuals with Prader-Willi syndrome (PWS) to physical exercise, and on the effectiveness of long-term exercise interventions to improve the clinical manifestat …
OBJECTIVE: The aim of this systematic review was to summarize evidence on the acute responses of individuals with Prader-Willi …
Autism spectrum disorder in Prader-Willi syndrome: A systematic review.
Bennett JA, Germani T, Haqq AM, Zwaigenbaum L. Bennett JA, et al. Am J Med Genet A. 2015 Dec;167A(12):2936-44. doi: 10.1002/ajmg.a.37286. Epub 2015 Aug 29. Am J Med Genet A. 2015. PMID: 26331980 Review.
Prader-Willi syndrome (PWS) is a rare genetic disorder that results from lack of expression of paternally-derived genes on chromosome 15q11-13; caused by a deletion (DEL), uniparental disomy (UPD), or a rare imprinting center defect. ...
Prader-Willi syndrome (PWS) is a rare genetic disorder that results from lack of expression of paternally-derived genes …
Mouse models of Prader-Willi Syndrome: a systematic review.
Bervini S, Herzog H. Bervini S, et al. Front Neuroendocrinol. 2013 Apr;34(2):107-19. doi: 10.1016/j.yfrne.2013.01.002. Epub 2013 Feb 4. Front Neuroendocrinol. 2013. PMID: 23391702 Review.
Prader-Willi Syndrome (PWS) is a neurodevelopmental genetic disorder caused by loss of expression of imprinted, paternally inherited genes on chromosome 15q11q13. ...
Prader-Willi Syndrome (PWS) is a neurodevelopmental genetic disorder caused by loss of expression of imprinted, paterna …
Psychotropic treatments in Prader-Willi syndrome: a critical review of published literature.
Bonnot O, Cohen D, Thuilleaux D, Consoli A, Cabal S, Tauber M. Bonnot O, et al. Eur J Pediatr. 2016 Jan;175(1):9-18. doi: 10.1007/s00431-015-2670-x. Epub 2015 Nov 19. Eur J Pediatr. 2016. PMID: 26584571 Review.
Prader-Willi syndrome (PWS) is a rare genetic syndrome. The phenotype includes moderate to intellectual disability, dysmorphia, obesity, and behavioral disturbances (e.g., hetero and self-injurious behaviors, hyperphagia, psychosis). ...Further randomized con …
Prader-Willi syndrome (PWS) is a rare genetic syndrome. The phenotype includes moderate to intellectual disability, dys …
The efficacy of intranasal oxytocin in patients with Prader-Willi syndrome: A systematic review and meta-analysis.
Shalma NM, Alsharabasy MA, Taha AM, Alsawareah A, Manirambona E, Ahmed SK, Mohamed MR, Taha NA, Abd-ElGawad M. Shalma NM, et al. Diabetes Metab Syndr. 2023 Feb;17(2):102711. doi: 10.1016/j.dsx.2023.102711. Epub 2023 Feb 4. Diabetes Metab Syndr. 2023. PMID: 36774885 Review.
BACKGROUND AND AIMS: Prader-Willi Syndrome (PWS) is a rare genetic disease. Oxytocin is a neuropeptide hormone that impacts fear, and social recognition. ...METHODS: We conducted a systematic literature search on Pubmed, Web of Science, and Scopus from incept …
BACKGROUND AND AIMS: Prader-Willi Syndrome (PWS) is a rare genetic disease. Oxytocin is a neuropeptide hormone that imp …
Growth Hormone Treatment for Adults With Prader-Willi Syndrome: A Meta-Analysis.
Rosenberg AGW, Passone CGB, Pellikaan K, Damiani D, van der Lely AJ, Polak M, Bernardo WM, de Graaff LCG. Rosenberg AGW, et al. J Clin Endocrinol Metab. 2021 Sep 27;106(10):3068-3091. doi: 10.1210/clinem/dgab406. J Clin Endocrinol Metab. 2021. PMID: 34105729 Free PMC article.
CONTEXT: Features of Prader-Willi syndrome (PWS) overlap with features of growth hormone (GH) deficiency, like small hands and feet, short stature, increased body fat, and low muscle mass and strength. ...
CONTEXT: Features of Prader-Willi syndrome (PWS) overlap with features of growth hormone (GH) deficiency, like small ha …
Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.
Rocha CF, Paiva CL. Rocha CF, et al. Genet Mol Res. 2014 Mar 31;13(1):2290-8. doi: 10.4238/2014.March.31.9. Genet Mol Res. 2014. PMID: 24737477 Free article. Review.
Prader-Willi syndrome (PWS) is caused by the lack of expression of genes located on paternal chromosome 15q11-q13. ...A search was carried out using the "National Center for Biotechnology Information" (www.pubmed.com) and "Scientific Electronic Library Online …
Prader-Willi syndrome (PWS) is caused by the lack of expression of genes located on paternal chromosome 15q11-q13. ...A …
Motor problems in Prader-Willi syndrome: a systematic review on body composition and neuromuscular functioning.
Reus L, Zwarts M, van Vlimmeren LA, Willemsen MA, Otten BJ, Nijhuis-van der Sanden MW. Reus L, et al. Neurosci Biobehav Rev. 2011 Jan;35(3):956-69. doi: 10.1016/j.neubiorev.2010.10.015. Epub 2010 Nov 4. Neurosci Biobehav Rev. 2011. PMID: 21056055 Free article. Review.
Motor problems in Prader-Willi syndrome (PWS) are presumably related to abnormal body composition and certain neuromuscular abnormalities. ...
Motor problems in Prader-Willi syndrome (PWS) are presumably related to abnormal body composition and certain neuromusc …
47 results