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1975 10
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1977 17
1978 9
1979 13
1980 21
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1983 35
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1986 31
1987 50
1988 27
1989 50
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1999 104
2000 106
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2002 81
2003 99
2004 102
2005 126
2006 131
2007 168
2008 144
2009 124
2010 158
2011 146
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4,732 results

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Page 1
Prader-Willi syndrome.
Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Cassidy SB, et al. Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Genet Med. 2012. PMID: 22237428 Free article. Review.
Prader-Willi syndrome is characterized by severe infantile hypotonia with poor suck and failure to thrive; hypogonadism causing genital hypoplasia and pubertal insufficiency; characteristic facial features; early-childhood onset obesity and hyperphagia; devel …
Prader-Willi syndrome is characterized by severe infantile hypotonia with poor suck and failure to thrive; hypogonadism …
Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Butler MG, Miller JL, Forster JL. Butler MG, et al. Curr Pediatr Rev. 2019;15(4):207-244. doi: 10.2174/1573396315666190716120925. Curr Pediatr Rev. 2019. PMID: 31333129 Free PMC article. Review.
BACKGROUND: Prader-Willi Syndrome (PWS) is a neurodevelopmental genomic imprinting disorder with lack of expression of genes inherited from the paternal chromosome 15q11-q13 region usually from paternal 15q11-q13 deletions (about 60%) or maternal uniparental …
BACKGROUND: Prader-Willi Syndrome (PWS) is a neurodevelopmental genomic imprinting disorder with lack of expression of …
Special Issue: Genetics of Prader-Willi Syndrome.
Godler DE, Butler MG. Godler DE, et al. Genes (Basel). 2021 Sep 16;12(9):1429. doi: 10.3390/genes12091429. Genes (Basel). 2021. PMID: 34573411 Free PMC article.
This Special Issue includes 15 peer-reviewed articles for publication by experts in Prader-Willi syndrome (PWS) and their reflective area of interest impacting this rare disorder [...]....
This Special Issue includes 15 peer-reviewed articles for publication by experts in Prader-Willi syndrome (PWS) and the …
Clinical Trials in Prader-Willi Syndrome: A Review.
Mahmoud R, Kimonis V, Butler MG. Mahmoud R, et al. Int J Mol Sci. 2023 Jan 21;24(3):2150. doi: 10.3390/ijms24032150. Int J Mol Sci. 2023. PMID: 36768472 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecular genetic classes. ...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecular genetic classes …
Prader-Willi syndrome: Hormone therapies.
Tauber M, Diene G. Tauber M, et al. Handb Clin Neurol. 2021;181:351-367. doi: 10.1016/B978-0-12-820683-6.00026-9. Handb Clin Neurol. 2021. PMID: 34238470 Review.
Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder linked to the lack of expression of specific maternally imprinted genes located in the chromosomal region 15q11-q13. ...
Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder linked to the lack of expression of specific …
Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
Angulo MA, Butler MG, Cataletto ME. Angulo MA, et al. J Endocrinol Invest. 2015 Dec;38(12):1249-63. doi: 10.1007/s40618-015-0312-9. Epub 2015 Jun 11. J Endocrinol Invest. 2015. PMID: 26062517 Free PMC article. Review.
INTRODUCTION: Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. ...CONCLUSIONS: Updated information regarding the early diagnosis and manage …
INTRODUCTION: Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused by lack of expression of g …
Prader-Willi syndrome: endocrine manifestations and management.
Alves C, Franco RR. Alves C, et al. Arch Endocrinol Metab. 2020 May-Jun;64(3):223-234. doi: 10.20945/2359-3997000000248. Arch Endocrinol Metab. 2020. PMID: 32555988 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of gene expression in the 15q11.2-q13 paternal chromosome. ...This review summarizes and updates the current knowledge about the prevention, diagnosis and treatment of endocrine manifesta …
Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of gene expression in the 15q11.2-q13 paternal …
Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.
Muscogiuri G, Barrea L, Faggiano F, Maiorino MI, Parrillo M, Pugliese G, Ruggeri RM, Scarano E, Savastano S, Colao A; RESTARE. Muscogiuri G, et al. J Endocrinol Invest. 2021 Oct;44(10):2057-2070. doi: 10.1007/s40618-021-01574-9. Epub 2021 Apr 23. J Endocrinol Invest. 2021. PMID: 33891302 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a genetic disorder caused by the lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. ...
Prader-Willi syndrome (PWS) is a genetic disorder caused by the lack of expression of genes on the paternally inherited …
Prader-Willi Syndrome and Hypogonadism: A Review Article.
Noordam C, Höybye C, Eiholzer U. Noordam C, et al. Int J Mol Sci. 2021 Mar 8;22(5):2705. doi: 10.3390/ijms22052705. Int J Mol Sci. 2021. PMID: 33800122 Free PMC article. Review.
Prader-Labhart-Willi syndrome (PWS) is a rare genetic disorder characterized by intellectual disability, behavioural problems, hypothalamic dysfunction and specific dysmorphisms. ...
Prader-Labhart-Willi syndrome (PWS) is a rare genetic disorder characterized by intellectual disability, behavioural pr …
Prader-Willi Syndrome: The More We Know, the Less We Know.
Whitman BY. Whitman BY. Mo Med. 2024 May-Jun;121(3):235-241. Mo Med. 2024. PMID: 38854617 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a complex genetic neurodevelopmental disorder with multisystem impact and a unique behavior profile that evolves over the life span. ...
Prader-Willi syndrome (PWS) is a complex genetic neurodevelopmental disorder with multisystem impact and a unique behav …
4,732 results