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Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.Radiology|April 1, 1988
Adhesive capsulitis of the wrist: arthrographic diagnosisM D Maloney, D D Sauser, E C Hanson, et al.Neuromuscular Disorders : NMD|March 14, 2000
A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathyS R Hammans, D O Robinson, C Moutou, et al.Annals of Neurology|June 1, 1988
Somatostatin and neuropeptide Y concentrations in pathologically graded cases of Huntington's diseaseM F Beal, M F Mazurek, D W Ellison, et al.Journal of Clinical Pathology|February 1, 1994
AIDS presenting as focal segmental membranous glomerulopathyP S Bass, P J Garrett, D W Ellison, et al.British Journal of Cancer|April 16, 2002
Genetic abnormalities detected in ependymomas by comparative genomic hybridisationM Carter, J Nicholson, F Ross, et al.Journal of the Neurological Sciences|March 1, 1988
A detailed examination of substance P in pathologically graded cases of Huntington's diseaseM F Beal, D W Ellison, M F Mazurek, et al.Brain : a Journal of Neurology|October 1, 1995
Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellumK P Bhatia, P Brown, R Gregory, et al.Pediatric Neurosurgery|August 15, 2000
Management of choroid plexus tumours in children: 20 years experience at a single neurosurgical centreA W McEvoy, B N Harding, K P Phipps, et al.AJNR. American Journal of Neuroradiology|July 30, 2016
Relative ADC and Location Differ between Posterior Fossa Pilocytic Astrocytomas with and without Gangliocytic DifferentiationJ H Harreld, S N Hwang, I Qaddoumi, et al.Pageof 13