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

Year Number of Results
1977 3
1978 2
1980 3
1981 2
1982 2
1983 8
1984 2
1985 2
1986 3
1987 4
1988 3
1989 4
1990 2
1991 2
1992 1
1993 2
1994 3
1996 2
1997 5
1998 2
1999 4
2000 6
2001 6
2002 3
2003 5
2004 5
2005 1
2006 5
2007 4
2008 3
2009 6
2010 4
2011 2
2012 5
2013 6
2014 5
2015 9
2016 4
2017 8
2018 3
2019 2
2020 2
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Article type
Publication date

Similar Articles for PMID: 21187304

151 results
Results by year
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Page 1
Clinical report—health supervision for children with Prader-Willi syndrome.
McCandless SE; Committee on Genetics. McCandless SE, et al. Pediatrics. 2011 Jan;127(1):195-204. doi: 10.1542/peds.2010-2820. Epub 2010 Dec 27. Pediatrics. 2011. PMID: 21187304
[Care continuity for patients with Prader-Willi syndrome during transition from childhood to adulthood].
Saitoh S. Saitoh S. Nihon Rinsho. 2010 Jan;68(1):141-4. Nihon Rinsho. 2010. PMID: 20077807 Review. Japanese.
The genetics, diagnosis, and management of Prader-Willi syndrome.
Nativio DG. Nativio DG. J Pediatr Health Care. 2002 Nov-Dec;16(6):298-303. J Pediatr Health Care. 2002. PMID: 12436099 Review.
Prader-Willi syndrome: an update and review for the primary pediatrician.
Chen C, Visootsak J, Dills S, Graham JM Jr. Chen C, et al. Clin Pediatr (Phila). 2007 Sep;46(7):580-91. doi: 10.1177/0009922807299314. Epub 2007 May 23. Clin Pediatr (Phila). 2007. PMID: 17522286 Review.
Molecular diagnosis of Prader-Willi syndrome.
Pangkanon S. Pangkanon S. J Med Assoc Thai. 2003 Aug;86 Suppl 3:S510-6. J Med Assoc Thai. 2003. PMID: 14700141
[Prader-Labhart-Willi syndrome in infants].
Schmeling H, Gillessen-Kaesbach G, Schulte-Mattler U, Burdach S, Horneff G. Schmeling H, et al. Klin Padiatr. 2002 Mar-Apr;214(2):51-3. doi: 10.1055/s-2002-25265. Klin Padiatr. 2002. PMID: 11972309 German.
[Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
Santa María L, Curotto B, Cortés F, Rojas C, Alliende MA. Santa María L, et al. Rev Med Chil. 2001 Apr;129(4):367-74. Rev Med Chil. 2001. PMID: 11413988 Spanish.
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.
Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.
Lukusa T, Fryns JP. Lukusa T, et al. Genet Couns. 2000;11(2):119-26. Genet Couns. 2000. PMID: 10893663 Review.
[Prader-Willi syndrome in a young infant].
Hack WW, ten Houten R, Breslau-Suderius EJ, Halley DJ. Hack WW, et al. Ned Tijdschr Geneeskd. 1997 Oct 18;141(42):2025-8. Ned Tijdschr Geneeskd. 1997. PMID: 9550755 Dutch.
151 results
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