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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1979 1
1981 3
1983 6
1984 2
1985 3
1986 3
1987 3
1988 5
1989 3
1990 5
1991 3
1992 10
1993 18
1994 12
1995 11
1996 16
1997 20
1998 10
1999 25
2000 23
2001 29
2002 16
2003 14
2004 24
2005 24
2006 23
2007 28
2008 22
2009 19
2010 33
2011 21
2012 21
2013 28
2014 23
2015 21
2016 30
2017 35
2018 22
2019 23
2020 35
2021 38
2022 33
2023 27
2024 17

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727 results

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Page 1
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 …
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: Possibilities of Weight Gain Prevention and Treatment.
Erhardt É, Molnár D. Erhardt É, et al. Nutrients. 2022 May 6;14(9):1950. doi: 10.3390/nu14091950. Nutrients. 2022. PMID: 35565916 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a complex genetic disorder which involves the endocrine and neurologic systems, metabolism, and behavior. ...
Prader-Willi syndrome (PWS) is a complex genetic disorder which involves the endocrine and neurologic systems, metaboli
Clinical Indications for Growth Hormone Therapy.
Danowitz M, Grimberg A. Danowitz M, et al. Adv Pediatr. 2022 Aug;69(1):203-217. doi: 10.1016/j.yapd.2022.03.005. Epub 2022 Jun 17. Adv Pediatr. 2022. PMID: 35985710 Free PMC article. Review.
In the United States, there are 8 Food and Drug Administration (FDA)-approved indications for pediatric GH therapy: GH deficiency, Prader-Willi Syndrome, small for gestational age (SGA) without catch-up growth, idiopathic short stature, Turner syndrome
In the United States, there are 8 Food and Drug Administration (FDA)-approved indications for pediatric GH therapy: GH deficiency, Prader
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
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. ...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. ...
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review.
Butler MG. Butler MG. Int J Mol Sci. 2023 Feb 21;24(5):4271. doi: 10.3390/ijms24054271. Int J Mol Sci. 2023. PMID: 36901699 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism/hypogenitalism and developmental delay during infancy. ...The CYFIP1 gene encodes a protein as
Prader-Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as seve
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 …
Endocrine disorders in Prader-Willi syndrome: a model to understand and treat hypothalamic dysfunction.
Tauber M, Hoybye C. Tauber M, et al. Lancet Diabetes Endocrinol. 2021 Apr;9(4):235-246. doi: 10.1016/S2213-8587(21)00002-4. Epub 2021 Feb 26. Lancet Diabetes Endocrinol. 2021. PMID: 33647242 Review.
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss of expression of maternally imprinted genes located in the paternal chromosomal region, 15q11-13. Impaired hypothalamic development and function is the cause of most o
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss of expression of maternally
Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L, Chamberlain SJ. Kalsner L, et al. Pediatr Clin North Am. 2015 Jun;62(3):587-606. doi: 10.1016/j.pcl.2015.03.004. Epub 2015 Apr 22. Pediatr Clin North Am. 2015. PMID: 26022164 Free PMC article. Review.
Three distinct neurodevelopmental disorders arise primarily from deletions or duplications that occur at the 15q11-q13 locus: Prader-Willi syndrome, Angelman syndrome, and 15q11-q13 duplication syndrome. ...
Three distinct neurodevelopmental disorders arise primarily from deletions or duplications that occur at the 15q11-q13 locus: Prader- …
727 results