Campbell LE - Search Results

1

Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.

Sinderberry B, Brown S, Hammond P, Stevens AF, Schall U, Murphy DG, Murphy KC, Campbell LE. Sinderberry B, et al. Among authors: campbell le. Res Dev Disabil. 2013 Jan;34(1):116-25. doi: 10.1016/j.ridd.2012.07.025. Epub 2012 Aug 30. Res Dev Disabil. 2013. PMID: 22940165

2

3D analysis of facial morphology.

Hammond P, Hutton TJ, Allanson JE, Campbell LE, Hennekam RC, Holden S, Patton MA, Shaw A, Temple IK, Trotter M, Murphy KC, Winter RM. Hammond P, et al. Among authors: campbell le. Am J Med Genet A. 2004 May 1;126A(4):339-48. doi: 10.1002/ajmg.a.20665. Am J Med Genet A. 2004. PMID: 15098232

3

Discriminating power of localized three-dimensional facial morphology.

Hammond P, Hutton TJ, Allanson JE, Buxton B, Campbell LE, Clayton-Smith J, Donnai D, Karmiloff-Smith A, Metcalfe K, Murphy KC, Patton M, Pober B, Prescott K, Scambler P, Shaw A, Smith AC, Stevens AF, Temple IK, Hennekam R, Tassabehji M. Hammond P, et al. Among authors: campbell le. Am J Hum Genet. 2005 Dec;77(6):999-1010. doi: 10.1086/498396. Epub 2005 Oct 26. Am J Hum Genet. 2005. PMID: 16380911 Free PMC article.

4

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

Campbell LE, Daly E, Toal F, Stevens A, Azuma R, Catani M, Ng V, van Amelsvoort T, Chitnis X, Cutter W, Murphy DG, Murphy KC. Campbell LE, et al. Brain. 2006 May;129(Pt 5):1218-28. doi: 10.1093/brain/awl066. Epub 2006 Mar 28. Brain. 2006. PMID: 16569671

5

Primary and secondary neural networks of auditory prepulse inhibition: a functional magnetic resonance imaging study of sensorimotor gating of the human acoustic startle response.

Campbell LE, Hughes M, Budd TW, Cooper G, Fulham WR, Karayanidis F, Hanlon MC, Stojanov W, Johnston P, Case V, Schall U. Campbell LE, et al. Eur J Neurosci. 2007 Oct;26(8):2327-33. doi: 10.1111/j.1460-9568.2007.05858.x. Epub 2007 Oct 1. Eur J Neurosci. 2007. PMID: 17908169

6

A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome.

Campbell LE, Stevens A, Daly E, Toal F, Azuma R, Karmiloff-Smith A, Murphy DG, Murphy KC. Campbell LE, et al. Neuropsychologia. 2009 Mar;47(4):1034-44. doi: 10.1016/j.neuropsychologia.2008.10.029. Epub 2008 Nov 13. Neuropsychologia. 2009. PMID: 19061904

7

Brain structural differences associated with the behavioural phenotype in children with Williams syndrome.

Campbell LE, Daly E, Toal F, Stevens A, Azuma R, Karmiloff-Smith A, Murphy DG, Murphy KC. Campbell LE, et al. Brain Res. 2009 Mar 3;1258:96-107. doi: 10.1016/j.brainres.2008.11.101. Epub 2008 Dec 11. Brain Res. 2009. PMID: 19118537

8

Executive functions and memory abilities in children with 22q11.2 deletion syndrome.

Campbell LE, Azuma R, Ambery F, Stevens A, Smith A, Morris RG, Murphy DG, Murphy KC. Campbell LE, et al. Aust N Z J Psychiatry. 2010 Apr;44(4):364-71. doi: 10.3109/00048670903489882. Aust N Z J Psychiatry. 2010. PMID: 20307169

9

Visual scanning of faces in 22q11.2 deletion syndrome: Attention to the mouth or the eyes?

Campbell L, McCabe K, Leadbeater K, Schall U, Loughland C, Rich D. Campbell L, et al. Psychiatry Res. 2010 May 15;177(1-2):211-5. doi: 10.1016/j.psychres.2009.06.007. Epub 2010 Apr 9. Psychiatry Res. 2010. PMID: 20381171

10

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

Campbell LE, Stevens AF, McCabe K, Cruickshank L, Morris RG, Murphy DG, Murphy KC. Campbell LE, et al. J Neurodev Disord. 2011 Jun;3(2):152-61. doi: 10.1007/s11689-011-9082-7. Epub 2011 May 5. J Neurodev Disord. 2011. PMID: 21544568 Free PMC article.

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