Showing results (21-30 of 2,350) with videos related to

Sort By:
Pageof 235
Neuropathology and Applied Neurobiology|December 1, 1990
A human glioma cell line retaining expression of GFAP and gangliosides, recognized by A2B5 and LB1 antibodies, after prolonged passageJ C Knott, A J Edwards, R W Gullan, et al.
Neuropathology and Applied Neurobiology|January 1, 1988
The cranial arachnoid and pia mater in man: anatomical and ultrastructural observationsR Alcolado, R O Weller, E P Parrish, et al.
Neuropathology and Applied Neurobiology|March 23, 2021
Loss of the metabolism and sleep regulating neuronal populations expressing orexin and oxytocin in the hypothalamus in amyotrophic lateral sclerosisSanaz Gabery, Rebekah M Ahmed, Jashelle Caga, et al.
Neuropathology and Applied Neurobiology|September 16, 2011
Cellular protein quality control and the evolution of aggregates in spinocerebellar ataxia type 3 (SCA3)K Seidel, M Meister, G J Dugbartey, et al.
Neuropathology and Applied Neurobiology|August 1, 1990
Glutathione S-transferase in human brainP J Carder, R Hume, A A Fryer, et al.
Neuropathology and Applied Neurobiology|September 29, 2011
Cerebral subcortical small vessel disease and its relation to cognition in elderly subjects: a pathological study in the Oxford Project to Investigate Memory and Ageing (OPTIMA) cohortA Smallwood, A Oulhaj, C Joachim, et al.
Neuropathology and Applied Neurobiology|April 25, 2012
Characterization of MENX-associated pituitary tumoursI Marinoni, M Lee, S Mountford, et al.
Neuropathology and Applied Neurobiology|March 23, 2012
Regionally different immunoreactivity for Smurf2 and pSmad2/3 in TDP-43-positive inclusions of amyotrophic lateral sclerosisM Nakamura, S Kaneko, R Wate, et al.
Neuropathology and Applied Neurobiology|April 5, 2012
Neuropathology of the hippocampus in FTLD-Tau with Pick bodies: a study of the BrainNet Europe ConsortiumG G Kovacs, A J M Rozemuller, J C van Swieten, et al.
Neuropathology and Applied Neurobiology|April 1, 2011
Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypesB A Faucheux, E Morain, V Diouron, et al.
Pageof 235