Devile CJ - Search Results

1

Severe cerebellitis following methadone poisoning.

Mills F, MacLennan SC, Devile CJ, Saunders DE. Mills F, et al. Among authors: devile cj. Pediatr Radiol. 2008 Feb;38(2):227-9. doi: 10.1007/s00247-007-0635-6. Epub 2007 Oct 20. Pediatr Radiol. 2008. PMID: 17952429

2

Magnetic resonance imaging assessment of infantile myofibromatosis.

Counsell SJ, Devile C, Mercuri E, Allsop JM, Birch R, Muntoni F. Counsell SJ, et al. Clin Radiol. 2002 Jan;57(1):67-70. doi: 10.1053/crad.2001.0723. Clin Radiol. 2002. PMID: 11798206 No abstract available.

3

Severe iron deficiency anaemia and ischaemic stroke in children.

Munot P, De Vile C, Hemingway C, Gunny R, Ganesan V. Munot P, et al. Arch Dis Child. 2011 Mar;96(3):276-9. doi: 10.1136/adc.2010.189241. Epub 2010 Oct 27. Arch Dis Child. 2011. PMID: 21030379

4

Clinical neuroimaging features and outcome in molybdenum cofactor deficiency.

Vijayakumar K, Gunny R, Grunewald S, Carr L, Chong KW, DeVile C, Robinson R, McSweeney N, Prabhakar P. Vijayakumar K, et al. Pediatr Neurol. 2011 Oct;45(4):246-52. doi: 10.1016/j.pediatrneurol.2011.06.006. Pediatr Neurol. 2011. PMID: 21907887

5

New challenges in the growth field.

DeVile CJ, Albanese A, Thomas B, Stanhope R. DeVile CJ, et al. J Pediatr Endocrinol. 1993 Jul-Dec;6(3-4):295-301. doi: 10.1515/jpem.1993.6.3-4.295. J Pediatr Endocrinol. 1993. PMID: 7920997 Review.

6

Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?

Mercuri E, Sewry CA, Brown SC, Brockington M, Jungbluth H, DeVile C, Counsell S, Manzur A, Muntoni F. Mercuri E, et al. Neuropediatrics. 2000 Aug;31(4):186-9. doi: 10.1055/s-2000-7460. Neuropediatrics. 2000. PMID: 11071142

7

Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy.

Mercuri E, Rutherford M, De Vile C, Counsell S, Sewry C, Brown S, Bydder G, Dubowitz V, Muntoni F. Mercuri E, et al. Neuromuscul Disord. 2001 Apr;11(3):297-9. doi: 10.1016/s0960-8966(00)00190-5. Neuromuscul Disord. 2001. PMID: 11297945

8

A severity scoring tool to assess the neurological features of neuronopathic Gaucher disease.

Davies EH, Surtees R, DeVile C, Schoon I, Vellodi A. Davies EH, et al. J Inherit Metab Dis. 2007 Oct;30(5):768-82. doi: 10.1007/s10545-007-0595-x. Epub 2007 Sep 16. J Inherit Metab Dis. 2007. PMID: 17876722 Review.

9

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations.

Polke JM, Laurá M, Pareyson D, Taroni F, Milani M, Bergamin G, Gibbons VS, Houlden H, Chamley SC, Blake J, Devile C, Sandford R, Sweeney MG, Davis MB, Reilly MM. Polke JM, et al. Neurology. 2011 Jul 12;77(2):168-73. doi: 10.1212/WNL.0b013e3182242d4d. Epub 2011 Jun 29. Neurology. 2011. PMID: 21715711 Free PMC article.

10

Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens.

Hacohen Y, Wright S, Waters P, Agrawal S, Carr L, Cross H, De Sousa C, Devile C, Fallon P, Gupta R, Hedderly T, Hughes E, Kerr T, Lascelles K, Lin JP, Philip S, Pohl K, Prabahkar P, Smith M, Williams R, Clarke A, Hemingway C, Wassmer E, Vincent A, Lim MJ. Hacohen Y, et al. J Neurol Neurosurg Psychiatry. 2013 Jul;84(7):748-55. doi: 10.1136/jnnp-2012-303807. Epub 2012 Nov 22. J Neurol Neurosurg Psychiatry. 2013. PMID: 23175854 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results