Surgical diagnostic tests

Clinical course, pathological correlations, and outcome of biopsy proved inflammatory demyelinating disease
S J Pittock, R L McClelland, S J Achenbach, F Konig, A Bitsch, W Brück, H Lassmann, J E Parisi, B W Scheithauer, M Rodriguez, B G Weinshenker, C F Lucchinetti

Journal of Neurology, Neurosurgery & Psychiatry Dec 2005, 76 (12) 1693-1697; DOI: 10.1136/jnnp.2004.060624
Peripheral neuropathy in metachromatic leucodystrophy. A study of 40 cases from south India
P S Bindu, A Mahadevan, A B Taly, R Christopher, N Gayathri, S K Shankar

Journal of Neurology, Neurosurgery & Psychiatry Dec 2005, 76 (12) 1698-1701; DOI: 10.1136/jnnp.2005.063776
Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy
F L Mastaglia, K J Nowak, R Stell, B A Phillips, J E Edmondston, S M Dorosz, S D Wilton, J Hallmayer, B A Kakulas, N G Laing

Journal of Neurology, Neurosurgery & Psychiatry Aug 1999, 67 (2) 174-179; DOI: 10.1136/jnnp.67.2.174
Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3
Rita Horvath, Birgit Czermin, Sweena Gulati, Stephanie Demuth, Gunnar Houge, Angela Pyle, Christine Dineiger, Emma L Blakely, Adam Hassani, Charlotte Foley, Michael Brodhun, Karin Storm, Janbernd Kirschner, Grainne S Gorman, Hanns Lochmüller, Elke Holinski-Feder, Robert W Taylor, Patrick F Chinnery

Journal of Neurology, Neurosurgery & Psychiatry Feb 2012, 83 (2) 174-178; DOI: 10.1136/jnnp-2011-301258
Visualisation of the circumventricular organs by fluorescence endoscopy
S Kubo, T Inui, K Yamazato

Journal of Neurology, Neurosurgery & Psychiatry Feb 2004, 75 (2) 180; DOI: 10.1136/jnnp.2003.023952
A novel NGFB point mutation: a phenotype study of heterozygous patients
J Minde, T Andersson, M Fulford, M Aguirre, I Nennesmo, I Nilsson Remahl, O Svensson, M Holmberg, G Toolanen, G Solders

Journal of Neurology, Neurosurgery & Psychiatry Feb 2009, 80 (2) 188-195; DOI: 10.1136/jnnp.2007.136051
Vertebral sarcoidosis mimicking metastases
C M Rice, V Beric, S Love, N J Scolding

Journal of Neurology, Neurosurgery & Psychiatry Feb 2011, 82 (2) 188; DOI: 10.1136/jnnp.2009.204636
A novel amyloidogenic transthyretin variant, Gly53Ala, associated with intermittent headaches and ataxia
C Douglass, K Suvarna, M M Reilly, P N Hawkins, M Hadjivassiliou

Journal of Neurology, Neurosurgery & Psychiatry Feb 2007, 78 (2) 193-195; DOI: 10.1136/jnnp.2006.093500
Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system?
D Caparros-Lefebvre, A Destée, H Petit

Journal of Neurology, Neurosurgery & Psychiatry Aug 1997, 63 (2) 196-203; DOI: 10.1136/jnnp.63.2.196
Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype
J Berciano, E Gallardo, R Domínguez-Perles, E Gallardo, A García, R García-Barredo, O Combarros, J Infante, I Illa

Journal of Neurology, Neurosurgery & Psychiatry Feb 2008, 79 (2) 205-208; DOI: 10.1136/jnnp.2007.125435

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