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F Chapon

Showing results (91-100 of 104) with videos related to

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Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
The Neuroradiology Journal|September 25, 2013
Five-Year Longitudinal MRI Follow-up and (1)H Single Voxel MRS in 14 patients with Gliomatosis Treated with Temodal, Radiotherapy and Antiangiogenic TherapyJ M Constans, S Collet, F Kauffmann, et al.
European Neurology|January 1, 1997
New mutations in the X-linked form of Charcot-Marie-Tooth diseaseP Latour, A Fabreguette, C Ressot, et al.
Molecular Syndromology|June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple MeningiomasF Riant, F Bergametti, H-D Fournier, et al.
Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.
Neuropathology and Applied Neurobiology|June 24, 2011
Utility of Ki67 immunostaining in the grading of pineal parenchymal tumours: a multicentre studyM Fèvre-Montange, A Vasiljevic, D Frappaz, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Pageof 11

Showing results (91-100 of 104) with videos related to

Sort By:
Pageof 11
Revue Neurologique|June 9, 2000
[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene]M Fardeau, P Vicart, A Caron, et al.
Clinical Genetics|November 6, 2007
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decayM Krahn, C Pécheux, F Chapon, et al.
Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
The Neuroradiology Journal|September 25, 2013
Five-Year Longitudinal MRI Follow-up and (1)H Single Voxel MRS in 14 patients with Gliomatosis Treated with Temodal, Radiotherapy and Antiangiogenic TherapyJ M Constans, S Collet, F Kauffmann, et al.
European Neurology|January 1, 1997
New mutations in the X-linked form of Charcot-Marie-Tooth diseaseP Latour, A Fabreguette, C Ressot, et al.
Molecular Syndromology|June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple MeningiomasF Riant, F Bergametti, H-D Fournier, et al.
Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.
Neuropathology and Applied Neurobiology|June 24, 2011
Utility of Ki67 immunostaining in the grading of pineal parenchymal tumours: a multicentre studyM Fèvre-Montange, A Vasiljevic, D Frappaz, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Pageof 11