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Diagnosis of sporadic neurofibromatosis type 2 in the paediatric population.
Anand G, Vasallo G, Spanou M, Thomas S, Pike M, Kariyawasam DS, Mehta S, Parry A, Durie-Gair J, Nicholson J, Lascelles K, Everett V, Gibbon FM, Jarvis N, Elston J, Evans DG, Halliday D. Anand G, et al. Among authors: pike m. Arch Dis Child. 2018 May;103(5):463-469. doi: 10.1136/archdischild-2017-313154. Epub 2018 Mar 13. Arch Dis Child. 2018. PMID: 29535107
It is all in the history, or is it?
Anand G, Jayawant S, McShane T, Pike M. Anand G, et al. Among authors: pike m. Arch Dis Child Educ Pract Ed. 2012 Feb;97(1):17-22. doi: 10.1136/adc.2010.202986. Epub 2011 Jun 22. Arch Dis Child Educ Pract Ed. 2012. PMID: 21697234 No abstract available.
Electroclinical outcome of children referred with suspected absence seizures.
Anand G, Padeniya A, Jain R, Hasan N, Jayawant S, Pike M, McShane T, Zaiwalla Z. Anand G, et al. Among authors: pike m. Arch Dis Child. 2011 Oct;96(10):987-8. doi: 10.1136/archdischild-2011-300531. Epub 2011 Sep 8. Arch Dis Child. 2011. PMID: 21908420 No abstract available.
Milder phenotypes of glucose transporter type 1 deficiency syndrome.
Anand G, Padeniya A, Hanrahan D, Scheffer H, Zaiwalla Z, Cox D, Mann N, Hewertson J, Price S, Nemeth A, Arsov T, Scheffer I, Jayawant S, Pike M, McShane T. Anand G, et al. Among authors: pike m. Dev Med Child Neurol. 2011 Jul;53(7):664-8. doi: 10.1111/j.1469-8749.2011.03949.x. Epub 2011 Mar 24. Dev Med Child Neurol. 2011. PMID: 21649651 Free article.
946 results