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Neonatal epileptic encephalopathy.
Clayton PT, Surtees RA, DeVile C, Hyland K, Heales SJ. Clayton PT, et al. Among authors: devile c. Lancet. 2003 May 10;361(9369):1614. doi: 10.1016/s0140-6736(03)13312-0. Lancet. 2003. PMID: 12747882 No abstract available.
Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.
Sadleir LG, Mountier EI, Gill D, Davis S, Joshi C, DeVile C, Kurian MA; DDD Study; Mandelstam S, Wirrell E, Nickels KC, Murali HR, Carvill G, Myers CT, Mefford HC, Scheffer IE. Sadleir LG, et al. Among authors: devile c. Neurology. 2017 Sep 5;89(10):1035-1042. doi: 10.1212/WNL.0000000000004331. Epub 2017 Aug 9. Neurology. 2017. PMID: 28794249 Free PMC article.
Randomized, controlled trial of miglustat in Gaucher's disease type 3.
Schiffmann R, Fitzgibbon EJ, Harris C, DeVile C, Davies EH, Abel L, van Schaik IN, Benko W, Timmons M, Ries M, Vellodi A. Schiffmann R, et al. Among authors: devile c. Ann Neurol. 2008 Nov;64(5):514-22. doi: 10.1002/ana.21491. Ann Neurol. 2008. PMID: 19067373 Free PMC article. Clinical Trial.
Bilateral giant retinal tears in Osteogenesis Imperfecta.
Scollo P, Snead MP, Richards AJ, Pollitt R, DeVile C. Scollo P, et al. Among authors: devile c. BMC Med Genet. 2018 Jan 12;19(1):8. doi: 10.1186/s12881-018-0521-0. BMC Med Genet. 2018. PMID: 29329516 Free PMC article.
Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta.
Hill M, Lewis C, Riddington M, Crowe B, DeVile C, David AL, Semler O, Westgren M, Götherström C, Chitty LS. Hill M, et al. Among authors: devile c. Eur J Hum Genet. 2019 Aug;27(8):1244-1253. doi: 10.1038/s41431-019-0387-4. Epub 2019 Mar 27. Eur J Hum Genet. 2019. PMID: 30918362 Free PMC article. Clinical Trial.
57 results