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E Tournier-Lasserve

Showing results (71-80 of 100) with videos related to

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Arthritis and Rheumatism|October 19, 1999
Poly(ADP-ribose) polymerase alleles in French Caucasians are associated neither with lupus nor with primary antiphospholipid syndrome. GRAID Research Group. Group for Research on Auto-Immune DisordersO Delrieu, M Michel, C Francès, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureM Vérin, Y Rolland, F Landgraf, 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.
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.
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.
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.
Neurology|March 26, 2003
Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutationS M Greenberg, Y Shin, T J Grabowski, et al.
Neurology|June 20, 1998
SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia onlyJ K Mellies, T Bäumer, J A Müller, 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.
Pageof 10

Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
Arthritis and Rheumatism|October 19, 1999
Poly(ADP-ribose) polymerase alleles in French Caucasians are associated neither with lupus nor with primary antiphospholipid syndrome. GRAID Research Group. Group for Research on Auto-Immune DisordersO Delrieu, M Michel, C Francès, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1995
New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical featureM Vérin, Y Rolland, F Landgraf, 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.
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.
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.
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.
Neurology|March 26, 2003
Hemorrhagic stroke associated with the Iowa amyloid precursor protein mutationS M Greenberg, Y Shin, T J Grabowski, et al.
Neurology|June 20, 1998
SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia onlyJ K Mellies, T Bäumer, J A Müller, 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.
Pageof 10