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F Chapon

Showing results (81-90 of 104) with videos related to

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European Journal of Nuclear Medicine|August 22, 2000
Non-invasive grading of oligodendrogliomas: correlation between in vivo metabolic pattern and histopathologyJ M Derlon, F Chapon, M H Noël, et al.
Clinical Chemistry|July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12A Vandenberghe, P Latour, G Chauplannaz, et al.
Muscle & Nerve|January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B diseaseP Sindou, J M Vallat, F Chapon, et al.
Neurology|March 26, 2003
Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutationS M Greenberg, Y Shin, T J Grabowski, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 31, 2007
Multiparametric differentiation of posterior fossa tumors in children using diffusion-weighted imaging and short echo-time 1H-MR spectroscopyJ F Schneider, S Confort-Gouny, A Viola, et al.
La Revue De Medecine Interne|October 30, 2010
[Confusion in a 60-year-old man]L Chiche, K Mazodier, S Genot, et al.
Journal De Radiologie|March 24, 2005
[Stent-graft treatment of a ruptured aortic graft: a case report]V Vidal, P Amabile, A Jacquier, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|February 24, 2007
Infratentorial pediatric brain tumors: the value of new imaging modalitiesJ F Schneider, A Viola, S Confort-Gouny, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
European Journal of Nuclear Medicine|August 22, 2000
Non-invasive grading of oligodendrogliomas: correlation between in vivo metabolic pattern and histopathologyJ M Derlon, F Chapon, M H Noël, et al.
Clinical Chemistry|July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12A Vandenberghe, P Latour, G Chauplannaz, et al.
Muscle & Nerve|January 12, 1999
Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B diseaseP Sindou, J M Vallat, F Chapon, et al.
Neurology|March 26, 2003
Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutationS M Greenberg, Y Shin, T J Grabowski, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 31, 2007
Multiparametric differentiation of posterior fossa tumors in children using diffusion-weighted imaging and short echo-time 1H-MR spectroscopyJ F Schneider, S Confort-Gouny, A Viola, et al.
La Revue De Medecine Interne|October 30, 2010
[Confusion in a 60-year-old man]L Chiche, K Mazodier, S Genot, et al.
Journal De Radiologie|March 24, 2005
[Stent-graft treatment of a ruptured aortic graft: a case report]V Vidal, P Amabile, A Jacquier, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|February 24, 2007
Infratentorial pediatric brain tumors: the value of new imaging modalitiesJ F Schneider, A Viola, S Confort-Gouny, et al.
Nature Genetics|September 10, 1998
A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathyP Vicart, A Caron, P Guicheney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Pageof 11