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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 9, 2008
Hypericin uptake: a prognostic marker for survival in high-grade gliomaR Ritz, M Müller, K Dietz, et al.Neuropediatrics|December 19, 2009
Andermann syndrome can be a phenocopy of hereditary motor and sensory neuropathy--report of a discordant sibship with a compound heterozygous mutation of the KCC3 geneS Rudnik-Schöneborn, U Hehr, T von Kalle, et al.Neuropathology and Applied Neurobiology|February 4, 2009
The microglial/macrophagic response at the tumour-brain border of invasive meningiomasS Grund, J Schittenhelm, F Roser, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2000
Altered expression of calcium- and apoptosis-regulating proteins in multiple system atrophy Purkinje cellsU Wüllner, M Weller, J Kornhuber, et al.Journal of Neuropathology and Experimental Neurology|April 12, 2000
Allograft inflammatory factor-1 is expressed by macrophages in injured skeletal muscle and abrogates proliferation and differentiation of satellite cellsR Kuschel, M H Deininger, R Meyermann, et al.Neuropediatrics|June 21, 2001
Proton MR spectroscopy reveals lactate in infantile neuroaxonal dystrophy (INAD)I Mader, I Krägeloh-Mann, U Seeger, et al.Brain : a Journal of Neurology|May 13, 1998
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2K Bushby, L V Anderson, C Pollitt, et al.Neuropathology and Applied Neurobiology|March 16, 2007
The astrocytic response towards invasive meningiomasL Zeltner, J Schittenhelm, M Mittelbronn, et al.Skeletal Radiology|July 16, 2008
MR findings in patients with disabling musculocutaneous chronic graft-versus-host diseaseM Horger, A Boss, W Bethge, et al.Neuromuscular Disorders : NMD|April 12, 2001
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approachC Pollitt, L V Anderson, R Pogue, et al.Pageof 12