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Human Molecular Genetics|January 15, 2013
Altered localization, abnormal modification and loss of function of Sigma receptor-1 in amyotrophic lateral sclerosisJ Prause, A Goswami, I Katona, et al.Archives of Neurology|July 1, 1992
Increased metallothionein in the liver and kidney of patients with amyotrophic lateral sclerosisP A Sillevis Smitt, H van Beek, A J Baars, et al.Biochemical and Biophysical Research Communications|August 21, 2001
GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytomaD A Vandeputte, C B Meije, M van Dartel, et al.Journal of Cancer Research and Clinical Oncology|January 12, 2001
Additive cytotoxic effect of cisplatin and X-irradiation on human glioma cell cultures derived from biopsy-tissueF Fehlauer, A D Barten-Van Rijbroek, L J Stalpers, et al.Epilepsy Research|November 21, 2007
Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complexK Boer, F Jansen, M Nellist, et al.Annals of Neurology|May 1, 1996
A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvementA J van der Kooi, T M Ledderhof, W G de Voogt, et al.Neuropathology and Applied Neurobiology|November 16, 2004
Neurotrophin receptor immunoreactivity in the hippocampus of patients with mesial temporal lobe epilepsyF Ozbas-Gerçeker, J A Gorter, S Redeker, et al.AJNR. American Journal of Neuroradiology|January 29, 2011
Correlating quantitative MR imaging with histopathology in X-linked adrenoleukodystrophyJ P van der Voorn, P J W Pouwels, J M Powers, et al.Neuroscience|April 18, 2003
Expression and cellular distribution of multidrug transporter proteins in two major causes of medically intractable epilepsy: focal cortical dysplasia and glioneuronal tumorsE Aronica, J A Gorter, G H Jansen, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1G J Jöbsis, J W Weber, P G Barth, et al.Pageof 21