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Year Number of Results
1945 1
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1948 6
1949 5
1950 9
1951 5
1952 5
1953 8
1954 5
1955 11
1956 12
1957 6
1958 6
1959 15
1960 7
1961 9
1962 6
1963 12
1964 14
1965 7
1966 12
1967 15
1968 23
1969 17
1970 18
1971 28
1972 16
1973 17
1974 25
1975 22
1976 21
1977 29
1978 25
1979 24
1980 34
1981 25
1982 33
1983 46
1984 39
1985 30
1986 43
1987 61
1988 33
1989 56
1990 56
1991 59
1992 71
1993 88
1994 78
1995 85
1996 97
1997 109
1998 120
1999 111
2000 120
2001 109
2002 90
2003 103
2004 119
2005 138
2006 147
2007 184
2008 162
2009 139
2010 170
2011 156
2012 158
2013 177
2014 166
2015 218
2016 215
2017 191
2018 213
2019 195
2020 226
2021 268
2022 249
2023 230
2024 250
2025 229

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5,841 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 …
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 behavior profile th …
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 …
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 …
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.
A review of Prader-Willi syndrome.
Metzler S, Brown GR. Metzler S, et al. JAAPA. 2025 Feb 1;38(2):e1-e6. doi: 10.1097/01.JAA.0000000000000079. Epub 2024 Jan 23. JAAPA. 2025. PMID: 39846602 Review.
Prader-Willi syndrome is a rare and complex genetic disorder with multiple physical and behavioral characteristics, affecting endocrine, metabolic, and neurologic systems and producing a plethora of medical complications. ...
Prader-Willi syndrome is a rare and complex genetic disorder with multiple physical and behavioral characteristics, affecting endocri …
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.
Ward OC. Ward OC. Lancet. 2000 Nov 25;356(9244):1856. doi: 10.1016/S0140-6736(05)73324-9. Lancet. 2000. PMID: 11117944 No abstract available.
The Prader-Willi syndrome.
Donaldson MD, Chu CE, Cooke A, Wilson A, Greene SA, Stephenson JB. Donaldson MD, et al. Arch Dis Child. 1994 Jan;70(1):58-63. doi: 10.1136/adc.70.1.58. Arch Dis Child. 1994. PMID: 8110011 Free PMC article. Review. No abstract available.
5,841 results