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E Tournier

Showing results (111-120 of 155) with videos related to

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Neurology|May 10, 2000
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASILA Joutel, H Chabriat, K Vahedi, et al.
The Journal of Infectious Diseases|June 1, 1988
Intrathecal synthesis of antibodies to human T lymphotropic virus type I and the presence of IgG oligoclonal bands in the cerebrospinal fluid of patients with endemic tropical spastic paraparesisA Gessain, C Caudie, O Gout, et al.
Annals of Neurology|August 1, 1995
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)M Ragno, E Tournier-Lasserve, M G Fiori, et al.
Clinical Radiology|May 14, 2013
Natural history of cerebral dot-like cavernomasO Nikoubashman, M Wiesmann, E Tournier-Lasserve, et al.
Revue Neurologique|January 1, 1986
[Double-blind treatment of 49 cases of chronic multiple sclerosis using hyperbaric oxygen]F Lhermitte, E Roullet, O Lyon-Caen, et al.
Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.
Neurology|June 1, 1995
Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locusH Chabriat, E Tournier-Lasserve, K Vahedi, 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.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 9, 2022
Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotypeT Coste, C Aloui, F Petit, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1991
Restricted T-cell receptor V beta gene usage by myelin basic protein-specific T-cell clones in multiple sclerosis: predominant genes vary in individualsA Ben-Nun, R S Liblau, L Cohen, et al.
Pageof 16

Showing results (111-120 of 155) with videos related to

Sort By:
Pageof 16
Neurology|May 10, 2000
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASILA Joutel, H Chabriat, K Vahedi, et al.
The Journal of Infectious Diseases|June 1, 1988
Intrathecal synthesis of antibodies to human T lymphotropic virus type I and the presence of IgG oligoclonal bands in the cerebrospinal fluid of patients with endemic tropical spastic paraparesisA Gessain, C Caudie, O Gout, et al.
Annals of Neurology|August 1, 1995
An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)M Ragno, E Tournier-Lasserve, M G Fiori, et al.
Clinical Radiology|May 14, 2013
Natural history of cerebral dot-like cavernomasO Nikoubashman, M Wiesmann, E Tournier-Lasserve, et al.
Revue Neurologique|January 1, 1986
[Double-blind treatment of 49 cases of chronic multiple sclerosis using hyperbaric oxygen]F Lhermitte, E Roullet, O Lyon-Caen, et al.
Nature Genetics|March 1, 1993
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12E Tournier-Lasserve, A Joutel, J Melki, et al.
Neurology|June 1, 1995
Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locusH Chabriat, E Tournier-Lasserve, K Vahedi, 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.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 9, 2022
Rare metabolic disease mimicking COL4A1/COL4A2 fetal brain phenotypeT Coste, C Aloui, F Petit, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 1991
Restricted T-cell receptor V beta gene usage by myelin basic protein-specific T-cell clones in multiple sclerosis: predominant genes vary in individualsA Ben-Nun, R S Liblau, L Cohen, et al.
Pageof 16