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J P Brandel

Showing results (31-40 of 55) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1996
[Acute basal ganglia necrosis with favorable course during Mycoplasma encepahlitis]G Noseda, J P Harpey, J P Brandel, 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.
AJNR. American Journal of Neuroradiology|May 1, 2010
Combined diffusion imaging and MR spectroscopy in the diagnosis of human prion diseasesDamien Galanaud, S Haik, M G Linguraru, et al.
Journal of Clinical Epidemiology|August 15, 2000
European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factorsI Zerr, J P Brandel, C Masullo, et al.
Neurology|October 16, 1999
Incubation period of Creutzfeldt-Jakob disease in human growth hormone recipients in FranceJ Huillard d'Aignaux, D Costagliola, J Maccario, et al.
Neurology|May 7, 2010
Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticusB Lapergue, S Demeret, V Denys, et al.
Neurology|April 13, 2000
Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP geneJ J Hauw, V Sazdovitch, J L Laplanche, et al.
Neurology|December 30, 2004
Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effectsS Haïk, J P Brandel, D Salomon, et al.
Neurology|January 1, 1997
Accuracy of the clinical diagnosis of corticobasal degeneration: a clinicopathologic studyI Litvan, Y Agid, C Goetz, et al.
Archives of Neurology|August 1, 1997
What is the accuracy of the clinical diagnosis of multiple system atrophy? A clinicopathologic studyI Litvan, C G Goetz, J Jankovic, et al.
Pageof 6

Showing results (31-40 of 55) with videos related to

Sort By:
Pageof 6
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1996
[Acute basal ganglia necrosis with favorable course during Mycoplasma encepahlitis]G Noseda, J P Harpey, J P Brandel, 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.
AJNR. American Journal of Neuroradiology|May 1, 2010
Combined diffusion imaging and MR spectroscopy in the diagnosis of human prion diseasesDamien Galanaud, S Haik, M G Linguraru, et al.
Journal of Clinical Epidemiology|August 15, 2000
European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factorsI Zerr, J P Brandel, C Masullo, et al.
Neurology|October 16, 1999
Incubation period of Creutzfeldt-Jakob disease in human growth hormone recipients in FranceJ Huillard d'Aignaux, D Costagliola, J Maccario, et al.
Neurology|May 7, 2010
Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticusB Lapergue, S Demeret, V Denys, et al.
Neurology|April 13, 2000
Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP geneJ J Hauw, V Sazdovitch, J L Laplanche, et al.
Neurology|December 30, 2004
Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effectsS Haïk, J P Brandel, D Salomon, et al.
Neurology|January 1, 1997
Accuracy of the clinical diagnosis of corticobasal degeneration: a clinicopathologic studyI Litvan, Y Agid, C Goetz, et al.
Archives of Neurology|August 1, 1997
What is the accuracy of the clinical diagnosis of multiple system atrophy? A clinicopathologic studyI Litvan, C G Goetz, J Jankovic, et al.
Pageof 6