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An investigation into the relationship between vigabatrin, movement disorders, and brain magnetic resonance imaging abnormalities in children with infantile spasms.
Fong CY, Osborne JP, Edwards SW, Hemingway C, Hancock E, Johnson AL, Kennedy CR, Kneen R, Likeman M, Lux AL, Mordekar SR, Murugan V, Newton RW, Pike M, Quinn M, Spinty S, Vassallo G, Verity CM, Whitney A, O'Callaghan FJ. Fong CY, et al. Among authors: whitney a. Dev Med Child Neurol. 2013 Sep;55(9):862-7. doi: 10.1111/dmcn.12188. Epub 2013 Jun 22. Dev Med Child Neurol. 2013. PMID: 23789722 Free article.
Movement disorder emergencies in childhood.
Kirkham FJ, Haywood P, Kashyape P, Borbone J, Lording A, Pryde K, Cox M, Keslake J, Smith M, Cuthbertson L, Murugan V, Mackie S, Thomas NH, Whitney A, Forrest KM, Parker A, Forsyth R, Kipps CM. Kirkham FJ, et al. Among authors: whitney a. Eur J Paediatr Neurol. 2011 Sep;15(5):390-404. doi: 10.1016/j.ejpn.2011.04.005. Epub 2011 Aug 10. Eur J Paediatr Neurol. 2011. PMID: 21835657 Review.
Childhood presentation of COL4A1 mutations.
Shah S, Ellard S, Kneen R, Lim M, Osborne N, Rankin J, Stoodley N, van der Knaap M, Whitney A, Jardine P. Shah S, et al. Among authors: whitney a. Dev Med Child Neurol. 2012 Jun;54(6):569-74. doi: 10.1111/j.1469-8749.2011.04198.x. Epub 2012 Jan 16. Dev Med Child Neurol. 2012. PMID: 22574627 Free article. Review.
Intrathecal baclofen pumps in the management of hypertonia in childhood: a UK and Ireland wide survey.
Lodh R, Amin S, Ammar A, Bellis L, Brink P, Calisto A, Crimmins D, Eunson P, Forsyth RJ, Goodden J, Kaminska M, Kehoe J, Kirkpatrick M, Kumar R, Leonard J, Lording A, Martin K, Miller R, Mordekar SR, Pettorini B, Smith M, Smith R, Sneade C, Whitney A, Vloeberghs M, Zaki H, Lumsden DE. Lodh R, et al. Among authors: whitney a. Arch Dis Child. 2021 Dec;106(12):1202-1206. doi: 10.1136/archdischild-2020-321487. Epub 2021 Apr 14. Arch Dis Child. 2021. PMID: 33853760
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Jenkinson EM, Rodero MP, Kasher PR, Uggenti C, Oojageer A, Goosey LC, Rose Y, Kershaw CJ, Urquhart JE, Williams SG, Bhaskar SS, O'Sullivan J, Baerlocher GM, Haubitz M, Aubert G, Barañano KW, Barnicoat AJ, Battini R, Berger A, Blair EM, Brunstrom-Hernandez JE, Buckard JA, Cassiman DM, Caumes R, Cordelli DM, De Waele LM, Fay AJ, Ferreira P, Fletcher NA, Fryer AE, Goel H, Hemingway CA, Henneke M, Hughes I, Jefferson RJ, Kumar R, Lagae L, Landrieu PG, Lourenço CM, Malpas TJ, Mehta SG, Metz I, Naidu S, Õunap K, Panzer A, Prabhakar P, Quaghebeur G, Schiffmann R, Sherr EH, Sinnathuray KR, Soh C, Stewart HS, Stone J, Van Esch H, Van Mol CE, Vanderver A, Wakeling EL, Whitney A, Pavitt GD, Griffiths-Jones S, Rice GI, Revy P, van der Knaap MS, Livingston JH, O'Keefe RT, Crow YJ. Jenkinson EM, et al. Among authors: whitney a. Nat Genet. 2016 Oct;48(10):1185-92. doi: 10.1038/ng.3661. Epub 2016 Aug 29. Nat Genet. 2016. PMID: 27571260 Free PMC article.
213 results