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E Tournier-Lasserve

Showing results (81-90 of 100) with videos related to

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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.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Neurology|July 21, 2010
A hereditary moyamoya syndrome with multisystemic manifestationsD Hervé, P Touraine, A Verloes, et al.
Lancet (London, England)|January 5, 2002
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosisA Joutel, P Favrole, P Labauge, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 10, 2020
Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesionsP Maurice, L Guilbaud, J Garel, et al.
Neuropediatrics|December 3, 2011
COL4A1 mutations associated with a characteristic pattern of intracranial calcificationJ Livingston, D Doherty, S Orcesi, et al.
European Journal of Neurology|March 21, 2020
Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of NeurologyM Mancuso, M Arnold, A Bersano, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
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.
Annals of Neurology|December 24, 1997
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneityA Ducros, A Joutel, K Vahedi, et al.
Nature Genetics|October 3, 1999
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomasS Laberge-le Couteulx, H H Jung, P Labauge, et al.
Lancet (London, England)|December 6, 1997
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patientsA Joutel, K Vahedi, C Corpechot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7qL Notelet, F Chapon, S Khoury, et al.
Neurology|July 21, 2010
A hereditary moyamoya syndrome with multisystemic manifestationsD Hervé, P Touraine, A Verloes, et al.
Lancet (London, England)|January 5, 2002
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosisA Joutel, P Favrole, P Labauge, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 10, 2020
Prevalence of COL4A1 and COL4A2 mutations in severe fetal multifocal hemorrhagic and/or ischemic cerebral lesionsP Maurice, L Guilbaud, J Garel, et al.
Neuropediatrics|December 3, 2011
COL4A1 mutations associated with a characteristic pattern of intracranial calcificationJ Livingston, D Doherty, S Orcesi, et al.
European Journal of Neurology|March 21, 2020
Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of NeurologyM Mancuso, M Arnold, A Bersano, et al.
Pageof 10