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Arthritis Research & Therapy|July 4, 2014
Anti-MDA5 autoantibodies in juvenile dermatomyositis identify a distinct clinical phenotype: a prospective cohort studySarah L Tansley, Zoe E Betteridge, Harsha Gunawardena, et al.
Acta Neuropathologica Communications|June 5, 2016
Imaging Invasion: Micro-CT imaging of adamantinomatous craniopharyngioma highlights cell type specific spatial relationships of tissue invasionJohn R Apps, J Ciaran Hutchinson, Owen J Arthurs, et al.
Experimental Cell Research|June 16, 2009
Astrocytoma derived short-term cell cultures retain molecular signatures characteristic of the tumour in situNicola E Potter, K Phipps, W Harkness, et al.
Annals of Neurology|September 1, 2005
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriersPeter P Pramstaller, Michael G Schlossmacher, Thomas S Jacques, et al.
Cancer Research|July 27, 2013
Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumor propagation in vitroNico V Henriquez, Tim Forshew, Ruth Tatevossian, et al.
Clinical Genetics|June 11, 2016
Aneuploidy: the impact of chromosome imbalance on nuclear organization and overall genome expressionB Hervé, A Coussement, T Gilbert, et al.
Journal of Neuro-Oncology|January 7, 2010
Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisationSamantha J Ward, Katherine Karakoula, Kim P Phipps, et al.
Acta Neuropathologica|February 22, 2012
Identification of novel pathways involved in the pathogenesis of human adamantinomatous craniopharyngiomaCynthia L Andoniadou, Carles Gaston-Massuet, Rukmini Reddy, et al.
Genes, Chromosomes & Cancer|July 30, 2008
Real-time quantitative PCR analysis of pediatric ependymomas identifies novel candidate genes including TPR at 1q25 and CHIBBY at 22q12-q13Katherine Karakoula, Blanca Suarez-Merino, Samantha Ward, et al.
Neuromuscular Disorders : NMD|March 23, 2013
Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 geneNomazulu Dlamini, Dragana J Josifova, Simon M L Paine, et al.
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