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E Tournier

Showing results (131-140 of 155) with videos related to

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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.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 13, 2024
Autoimmune bullous diseases induced by cyclin-dependent kinase 4/6 inhibitors-first cohort from the EADV Task Force 'Dermatology for Cancer Patients'A Ortiz-Brugués, M Starace, F Bardazzi, 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|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.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
Annales De Dermatologie Et De Venereologie|May 27, 2020
[The role of new molecular tests in the diagnosis of melanoma in a setting of congenital nævus in an infant]M Masson Regnault, S Fraitag, L Lamant, et al.
Pageof 16

Showing results (131-140 of 155) with videos related to

Sort By:
Pageof 16
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.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 13, 2024
Autoimmune bullous diseases induced by cyclin-dependent kinase 4/6 inhibitors-first cohort from the EADV Task Force 'Dermatology for Cancer Patients'A Ortiz-Brugués, M Starace, F Bardazzi, 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|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.
Neurology|January 15, 2003
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathyK Vahedi, P Massin, J-P Guichard, et al.
Annales De Dermatologie Et De Venereologie|May 27, 2020
[The role of new molecular tests in the diagnosis of melanoma in a setting of congenital nævus in an infant]M Masson Regnault, S Fraitag, L Lamant, et al.
Pageof 16