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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2004 1
2005 7
2006 6
2007 7
2008 7
2009 9
2010 11
2011 4
2012 3
2013 7
2014 2
2015 1
2016 1
2024 0

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Search Results

61 results

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Page 1
Dopa responsive dystonia.
Low K, Harding T, Jardine P. Low K, et al. Among authors: jardine p. BMJ. 2010 Mar 4;340:c668. doi: 10.1136/bmj.c668. BMJ. 2010. PMID: 20203076 No abstract available.
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: jardine p. 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.
Fracture prevalence in Duchenne muscular dystrophy.
McDonald DG, Kinali M, Gallagher AC, Mercuri E, Muntoni F, Roper H, Jardine P, Jones DH, Pike MG. McDonald DG, et al. Among authors: jardine p. Dev Med Child Neurol. 2002 Oct;44(10):695-8. doi: 10.1017/s0012162201002778. Dev Med Child Neurol. 2002. PMID: 12418795 Free article.
Paediatric UK demyelinating disease longitudinal study (PUDDLS).
Absoud M, Cummins C, Chong WK, De Goede C, Foster K, Gunny R, Hemingway C, Jardine P, Kneen R, Likeman M, Lim MJ, Pike M, Sibtain N, Whitehouse WP, Wassmer E. Absoud M, et al. Among authors: jardine p. BMC Pediatr. 2011 Jul 28;11:68. doi: 10.1186/1471-2431-11-68. BMC Pediatr. 2011. PMID: 21798048 Free PMC article.
SGCE mutations cause psychiatric disorders: clinical and genetic characterization.
Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR. Peall KJ, et al. Among authors: jardine p. Brain. 2013 Jan;136(Pt 1):294-303. doi: 10.1093/brain/aws308. Brain. 2013. PMID: 23365103 Free PMC article.
Basal ganglia necrosis: a 'best-fit' approach.
Boca M, Lloyd K, Likeman M, Jardine P, Whone A. Boca M, et al. Among authors: jardine p. Pract Neurol. 2016 Dec;16(6):458-461. doi: 10.1136/practneurol-2016-001410. Epub 2016 Aug 8. Pract Neurol. 2016. PMID: 27503951
Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations.
Silveira-Moriyama L, Gardiner AR, Meyer E, King MD, Smith M, Rakshi K, Parker A, Mallick AA, Brown R, Vassallo G, Jardine PE, Guerreiro MM, Lees AJ, Houlden H, Kurian MA. Silveira-Moriyama L, et al. Among authors: jardine pe. Dev Med Child Neurol. 2013 Apr;55(4):327-34. doi: 10.1111/dmcn.12056. Epub 2013 Jan 30. Dev Med Child Neurol. 2013. PMID: 23363396 Free article.
Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort.
Hacohen Y, Absoud M, Woodhall M, Cummins C, De Goede CG, Hemingway C, Jardine PE, Kneen R, Pike MG, Whitehouse WP, Wassmer E, Waters P, Vincent A, Lim M; UK & Ireland Childhood CNS Inflammatory Demyelination Working Group. Hacohen Y, et al. Among authors: jardine pe. J Neurol Neurosurg Psychiatry. 2014 Apr;85(4):456-61. doi: 10.1136/jnnp-2013-306411. Epub 2013 Oct 16. J Neurol Neurosurg Psychiatry. 2014. PMID: 24133290
Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features.
Absoud M, Lim MJ, Chong WK, De Goede CG, Foster K, Gunny R, Hemingway C, Jardine PE, Kneen R, Likeman M, Nischal KK, Pike MG, Sibtain NA, Whitehouse WP, Cummins C, Wassmer E; UK and Ireland Childhood CNS Inflammatory Demyelination Working Group. Absoud M, et al. Among authors: jardine pe. Mult Scler. 2013 Jan;19(1):76-86. doi: 10.1177/1352458512445944. Epub 2012 Apr 19. Mult Scler. 2013. PMID: 22516794 Free PMC article.
61 results