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Showing results (81-90 of 142) with videos related to

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Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0554C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: spastic paraparesis. Accession #Hs0515C Depienne, C Tallaksen, J Y Lephay, et al.
Revue Neurologique|April 4, 2007
[Adult leukoencephalopathy caused by alpha-mannosidosis deficiency]G Castelnovo, T Levade, H M F Riise Stensland, et al.
Journal of Medical Genetics|August 2, 2005
Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial casesC Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hd0519C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0557C Depienne, C Tallaksen, J Y Lephay, et al.
Revue Neurologique|June 21, 2008
[Ma2 antibody and multiple mononeuropathies]X Ayrignac, G Castelnovo, E Landrault, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0556C Depienne, C Tallaksen, J Y Lephay, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|October 18, 2015
Use of quantitative susceptibility mapping (QSM) in progressive multifocal leukoencephalopathyC Carra-Dalliere, N Menjot de Champfleur, J Deverdun, et al.
Revue Neurologique|February 17, 2007
[Influence of acute aggravations on the development of long-term handicap in relapsing remitting multiple sclerosis: a clinical study in 99 patients]N Gaillard, P Fabro-Perray, J-L Faillie, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0554C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: spastic paraparesis. Accession #Hs0515C Depienne, C Tallaksen, J Y Lephay, et al.
Revue Neurologique|April 4, 2007
[Adult leukoencephalopathy caused by alpha-mannosidosis deficiency]G Castelnovo, T Levade, H M F Riise Stensland, et al.
Journal of Medical Genetics|August 2, 2005
Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial casesC Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hd0519C Depienne, C Tallaksen, J Y Lephay, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0557C Depienne, C Tallaksen, J Y Lephay, et al.
Revue Neurologique|June 21, 2008
[Ma2 antibody and multiple mononeuropathies]X Ayrignac, G Castelnovo, E Landrault, et al.
Human Genetics|February 14, 2007
Gene symbol: SPAST. Disease: Spastic paraparesis. Accession #Hm0556C Depienne, C Tallaksen, J Y Lephay, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|October 18, 2015
Use of quantitative susceptibility mapping (QSM) in progressive multifocal leukoencephalopathyC Carra-Dalliere, N Menjot de Champfleur, J Deverdun, et al.
Revue Neurologique|February 17, 2007
[Influence of acute aggravations on the development of long-term handicap in relapsing remitting multiple sclerosis: a clinical study in 99 patients]N Gaillard, P Fabro-Perray, J-L Faillie, et al.
Pageof 15