McAllister CJ - Search Results

1

Asymptomatic sleep abnormalities are a common early feature in patients with Huntington's disease.

Goodman AO, Rogers L, Pilsworth S, McAllister CJ, Shneerson JM, Morton AJ, Barker RA. Goodman AO, et al. Among authors: mcallister cj. Curr Neurol Neurosci Rep. 2011 Apr;11(2):211-7. doi: 10.1007/s11910-010-0163-x. Curr Neurol Neurosci Rep. 2011. PMID: 21103960

2

Responses to environmental enrichment differ with sex and genotype in a transgenic mouse model of Huntington's disease.

Wood NI, Carta V, Milde S, Skillings EA, McAllister CJ, Ang YL, Duguid A, Wijesuriya N, Afzal SM, Fernandes JX, Leong TW, Morton AJ. Wood NI, et al. Among authors: mcallister cj. PLoS One. 2010 Feb 12;5(2):e9077. doi: 10.1371/journal.pone.0009077. PLoS One. 2010. PMID: 20174443 Free PMC article.

3

Disruption of peripheral circadian timekeeping in a mouse model of Huntington's disease and its restoration by temporally scheduled feeding.

Maywood ES, Fraenkel E, McAllister CJ, Wood N, Reddy AB, Hastings MH, Morton AJ. Maywood ES, et al. Among authors: mcallister cj. J Neurosci. 2010 Jul 28;30(30):10199-204. doi: 10.1523/JNEUROSCI.1694-10.2010. J Neurosci. 2010. PMID: 20668203 Free PMC article.

4

Adaptation to experimental jet-lag in R6/2 mice despite circadian dysrhythmia.

Wood NI, McAllister CJ, Cuesta M, Aungier J, Fraenkel E, Morton AJ. Wood NI, et al. Among authors: mcallister cj. PLoS One. 2013;8(2):e55036. doi: 10.1371/journal.pone.0055036. Epub 2013 Feb 4. PLoS One. 2013. PMID: 23390510 Free PMC article.

5

The transition between the phenotypes of Prader-Willi syndrome during infancy and early childhood.

Butler JV, Whittington JE, Holland AJ, McAllister CJ, Goldstone AP. Butler JV, et al. Among authors: mcallister cj. Dev Med Child Neurol. 2010 Jun;52(6):e88-93. doi: 10.1111/j.1469-8749.2009.03530.x. Epub 2009 Dec 23. Dev Med Child Neurol. 2010. PMID: 20041936 Free article.

6

Defective mitochondrial function in vivo in skeletal muscle in adults with Down's syndrome: a 31P-MRS study.

Phillips AC, Sleigh A, McAllister CJ, Brage S, Carpenter TA, Kemp GJ, Holland AJ. Phillips AC, et al. Among authors: mcallister cj. PLoS One. 2013 Dec 31;8(12):e84031. doi: 10.1371/journal.pone.0084031. eCollection 2013. PLoS One. 2013. PMID: 24391872 Free PMC article.

7

Comparative analysis of synovial fluid and plasma proteomes in juvenile arthritis--proteomic patterns of joint inflammation in early stage disease.

Gibson DS, Blelock S, Curry J, Finnegan S, Healy A, Scaife C, McAllister C, Pennington S, Dunn M, Rooney M. Gibson DS, et al. J Proteomics. 2009 May 2;72(4):656-76. doi: 10.1016/j.jprot.2009.01.022. J Proteomics. 2009. PMID: 19367684 Free PMC article.

8

Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding.

McAllister CJ, Whittington JE, Holland AJ. McAllister CJ, et al. Int J Obes (Lond). 2011 Feb;35(2):188-97. doi: 10.1038/ijo.2010.139. Epub 2010 Aug 3. Int J Obes (Lond). 2011. PMID: 20680019 Review.

9

A short clinical overview of Prader-Willi syndrome.

McAllister CJ, Whittington JE. McAllister CJ, et al. Clin Obes. 2011 Aug;1(4-6):184-8. doi: 10.1111/j.1758-8111.2011.00022.x. Epub 2011 Sep 29. Clin Obes. 2011. PMID: 25585908

10

Growth hormone, gender and face shape in Prader-Willi syndrome.

de Souza MA, McAllister C, Suttie M, Perrotta C, Mattina T, Faravelli F, Forzano F, Holland A, Hammond P. de Souza MA, et al. Am J Med Genet A. 2013 Oct;161A(10):2453-63. doi: 10.1002/ajmg.a.36100. Epub 2013 Aug 5. Am J Med Genet A. 2013. PMID: 23918156

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