Literature DB >> 16156341

Prader-Willi syndrome.

Daniel J Wattendorf1, Maximilian Muenke.   

Abstract

To complement the 2005 Annual Clinical Focus on medical genomics, AFP is publishing a series of short reviews on genetic syndromes. 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.

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Mesh：

Year:  2005        PMID： 16156341

Source DB:  PubMed          Journal:  Am Fam Physician        ISSN： 0002-838X            Impact factor:   3.292


  7 in total

Review 1.  Modeling neurodevelopmental disorders using human neurons.

Authors:  Thanathom Chailangkarn; Allan Acab; Alysson Renato Muotri
Journal:  Curr Opin Neurobiol       Date:  2012-06-19       Impact factor: 6.627

2.  Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes.

Authors:  Jennifer Boyle; Malcolm Hawkins; David E Barton; Karen Meaney; Miriam Guitart; Anna O'Grady; Simon Tobi; Simon C Ramsden; Rob Elles; Elaine Gray; Paul Metcalfe; J Ross Hawkins
Journal:  Eur J Hum Genet       Date:  2011-05-18       Impact factor: 4.246

Review 3.  Proteins and proteases of Prader-Willi syndrome: a comprehensive review and perspectives.

Authors:  Sanjukta Basak; Ajoy Basak
Journal:  Biosci Rep       Date:  2022-06-30       Impact factor: 3.976

Review 4.  Skin manifestations of growth hormone-induced diseases.

Authors:  Christina Kanaka-Gantenbein; Christina Kogia; Mohamed Badawy Abdel-Naser; George P Chrousos
Journal:  Rev Endocr Metab Disord       Date:  2016-09       Impact factor: 6.514

5.  Inclusion of chiropractic care in multidisciplinary management of a child with Prader-Willi syndrome: a case report.

Authors:  Rebekah A Wittman; Sharon A Vallone
Journal:  J Chiropr Med       Date:  2009-12

6.  Clinical and genetic analysis for four Chinese families with Prader-Willi syndrome.

Authors:  Yu-wen Zhang; Hui-ying Jia; Jie Hong; Yan Ge; Hui-jie Zhang; Chun-fang Shen; Lei Ye; Bin Cui; Xiao-ying Li; Wei-qiong Gu; Yi-fei Zhang; Wei-qing Wang; Guang Ning
Journal:  Endocrine       Date:  2009-05-07       Impact factor: 3.633

7.  Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation.

Authors:  Boris V Skryabin; Leonid V Gubar; Birte Seeger; Jana Pfeiffer; Sergej Handel; Thomas Robeck; Elena Karpova; Timofey S Rozhdestvensky; Jürgen Brosius
Journal:  PLoS Genet       Date:  2007-12-28       Impact factor: 5.917
  7 in total

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