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F Riant

Showing results (11-20 of 17) with videos related to

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Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Revue Neurologique|October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian familyF Tinsa, I Bel Hadj, F Riant, et al.
Revue Neurologique|April 7, 2015
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 geneA Bisserbe, G Tertian, C Buffet, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Neurology|June 10, 2009
Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutationsP Labauge, B Fontaine, J-P Neau, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, 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.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Revue Neurologique|September 16, 2019
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature reviewO Osman, P Labrune, P Reiner, et al.
Revue Neurologique|October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian familyF Tinsa, I Bel Hadj, F Riant, et al.
Revue Neurologique|April 7, 2015
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 geneA Bisserbe, G Tertian, C Buffet, et al.
Neurology|April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutationsK Vahedi, C Depienne, D Le Fort, et al.
Neurology|June 10, 2009
Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutationsP Labauge, B Fontaine, J-P Neau, et al.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, 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.
Pageof 2