Search research articles
Contact Us
Filters
Showing results (11-20 of 17) with videos related to
Page
of 2
Sort By:
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 review
O Osman, P Labrune, P Reiner, et al.
Revue Neurologique
|
October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian family
F 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 gene
A Bisserbe, G Tertian, C Buffet, et al.
Neurology
|
April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations
K Vahedi, C Depienne, D Le Fort, et al.
Neurology
|
June 10, 2009
Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations
P Labauge, B Fontaine, J-P Neau, et al.
Neurology
|
January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy
K Vahedi, P Massin, J-P Guichard, et al.
Molecular Syndromology
|
June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas
F Riant, F Bergametti, H-D Fournier, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 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 review
O Osman, P Labrune, P Reiner, et al.
Revue Neurologique
|
October 14, 2018
A novel large deletion in CCM1 gene in a Tunisian family
F 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 gene
A Bisserbe, G Tertian, C Buffet, et al.
Neurology
|
April 1, 2009
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations
K Vahedi, C Depienne, D Le Fort, et al.
Neurology
|
June 10, 2009
Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations
P Labauge, B Fontaine, J-P Neau, et al.
Neurology
|
January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy
K Vahedi, P Massin, J-P Guichard, et al.
Molecular Syndromology
|
June 27, 2013
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas
F Riant, F Bergametti, H-D Fournier, et al.
Page
of 2