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1955 11
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1959 15
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1963 12
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1966 12
1967 15
1968 23
1969 17
1970 18
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1972 16
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1974 25
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2009 139
2010 170
2011 156
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5,805 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; developmental delay …
Prader-Willi syndrome is characterized by severe infantile hypotonia with poor suck and failure to thrive; hypogonadism causing genit …
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 their reflective …
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 of the phenotyp …
Prader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting from the loss of expression of maternally imprinted gen …
Approach to the Patient With Prader-Willi Syndrome.
Höybye C, Tauber M. Höybye C, et al. J Clin Endocrinol Metab. 2022 May 17;107(6):1698-1705. doi: 10.1210/clinem/dgac082. J Clin Endocrinol Metab. 2022. PMID: 35150573 Free PMC article.
Prader-Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involving the hypothalamus. ...
Prader-Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involving the hypothalamus. ...
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.
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 advocated by p …
Prader-Willi syndrome.
Cassidy SB. Cassidy SB. J Med Genet. 1997 Nov;34(11):917-23. doi: 10.1136/jmg.34.11.917. J Med Genet. 1997. PMID: 9391886 Free PMC article. Review.
Prader-Willi syndrome is a complex disorder affecting multiple systems with many manifestations relating to hypothalamic insufficiency. ...Obesity and the behavioural problems are the major causes of morbidity and mortality. Prader-Willi syndrome is caused by abnorm …
Prader-Willi syndrome is a complex disorder affecting multiple systems with many manifestations relating to hypothalamic insufficienc …
Psychopathological disorders in Prader-Willi syndrome.
Guinovart M, Coronas R, Caixàs A. Guinovart M, et al. Endocrinol Diabetes Nutr (Engl Ed). 2019 Nov;66(9):579-587. doi: 10.1016/j.endinu.2019.03.004. Epub 2019 Apr 18. Endocrinol Diabetes Nutr (Engl Ed). 2019. PMID: 31006652 Review. English, Spanish.
Prader-Willi syndrome is a genetic disorder caused by chromosomal changes in segment 15q11-q13 including cognitive, mental, and behavioral symptoms, as well as a specific physical phenotype. ...Adequate understanding of the psychopathology associated to Prader-Willi …
Prader-Willi syndrome is a genetic disorder caused by chromosomal changes in segment 15q11-q13 including cognitive, mental, and behav …
Prader-Willi syndrome.
Cassidy SB. Cassidy SB. Curr Probl Pediatr. 1984 Jan;14(1):1-55. doi: 10.1016/0045-9380(84)90043-4. Curr Probl Pediatr. 1984. PMID: 6365470 Review. No abstract available.
Prader-Willi syndrome.
Wattendorf DJ, Muenke M. Wattendorf DJ, et al. Am Fam Physician. 2005 Sep 1;72(5):827-30. Am Fam Physician. 2005. PMID: 16156341 Free article. Review.
This series was designed to increase awareness of these diseases so that family physicians can recognize and diagnose children with these disorders and understand the type of care they might require in the future. This review discusses Prader-Willi syndrome....
This series was designed to increase awareness of these diseases so that family physicians can recognize and diagnose children with these di …
Prader-Willi syndrome.
Couper R. Couper R. J Paediatr Child Health. 1999 Aug;35(4):331-4. doi: 10.1046/j.1440-1754.1999.00397.x. J Paediatr Child Health. 1999. PMID: 10457284 Review.
Prader-Willi syndrome is a multi system disorder characterized by neonatal hypotonia, later obesity, hyperphagia and mental retardation. ...
Prader-Willi syndrome is a multi system disorder characterized by neonatal hypotonia, later obesity, hyperphagia and mental retardati …
5,805 results