Literature DB >> 25171992

Craniosynostosis syndromes.

Carolyn Dicus Brookes1, Brent A Golden1, Timothy A Turvey2.   

Abstract

Entities:  

Keywords:  Apert; Craniofacial dysostosis; Craniosynostosis syndromes; Crouzon; Muenke; Pfeiffer

Mesh：

Year:  2014        PMID： 25171992     DOI： 10.1016/j.cxom.2014.04.001

Source DB:  PubMed          Journal:  Atlas Oral Maxillofac Surg Clin North Am        ISSN： 1061-3315


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  5 in total

Review 1.  Understanding craniosynostosis as a growth disorder.

Authors:  Kevin Flaherty; Nandini Singh; Joan T Richtsmeier
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2016-03-22       Impact factor: 5.814

2.  C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.

Authors:  Ying Lin; Hongbin Gao; Siming Ai; Jacob V P Eswarakumar; Chuan Chen; Yi Zhu; Tao Li; Bingqian Liu; Xialin Liu; Lixia Luo; Hongye Jiang; Yonghao Li; Xiaoling Liang; Chenjin Jin; Xinhua Huang; Lin Lu
Journal:  Mol Med Rep       Date:  2017-08-14       Impact factor: 2.952

3.  An Unoperated Crouzon Family Treated with Monobloc Distraction: Challenges and Lessons.

Authors:  Justin Hart; Stephen Lu; Konstantinos Gasteratos; Kongkrit Chaiyasate
Journal:  Plast Reconstr Surg Glob Open       Date:  2021-11-02

Review 4.  Crouzon syndrome and the eye: An overview.

Authors:  Kasturi Bhattacharjee; Obaidur Rehman; Vatsalya Venkatraman; Don Kikkawa; Harsha Bhattacharjee; Rahul Gogoi; Aditi Mehta Grewal; Pragya Bhattacharjee
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

5.  FGFR2 Mutation p.Cys342Arg Enhances Mitochondrial Metabolism-Mediated Osteogenesis via FGF/FGFR-AMPK-Erk1/2 Axis in Crouzon Syndrome.

Authors:  Yidi Wang; Yue Liu; Haotian Chen; Xiaojing Liu; Yi Zhang; Yixiang Wang; Yan Gu
Journal:  Cells       Date:  2022-10-05       Impact factor: 7.666
  5 in total

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