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The Journal of Biological Chemistry|November 20, 2022
Lysyl hydroxylase 3-mediated post-translational modifications are required for proper biosynthesis of collagen α1α1α2(IV)Yoshihiro Ishikawa, Yuki Taga, Thibault Coste, et al.Annals of Neurology|October 17, 2006
Genotype-phenotype correlations in cerebral cavernous malformations patientsChristian Denier, Pierre Labauge, Françoise Bergametti, et al.Annals of Surgery|October 26, 2005
French women from multiplex abdominal aortic aneurysm families should be screenedClaire Le Hello, Fabien Koskas, Philippe Cluzel, et al.Journal of Stroke|October 12, 2022
Elderly CADASIL patients with intact neurological statusRuiting Zhang, Elisa Ouin, Lina Grosset, et al.Stroke|March 24, 2025
Identity-by-Descent Analysis Uncovering a Founder Event in a Novel Hereditary Small Vessel Cerebral DiseaseArnaud Maillard, Eva Pipiras, Philippe Jarnoux, et al.European Journal of Neurology|July 13, 2026
Late Cognitive or Mood Alterations With 'Status Cribrosum' and Diffuse White Matter Lesions: A New Cerebral Small Vessel Disease Phenotype Associated With Rare COL4A1 Variants Located Within Exon 23Hélène Morel, Sophie Dufourd-Delalande, William Bloch, et al.Annals of Neurology|February 3, 2004
Clinical features of cerebral cavernous malformations patients with KRIT1 mutationsChristian Denier, Pierre Labauge, Laurent Brunereau, et al.The Journal of Experimental Medicine|August 24, 2011
Developmental timing of CCM2 loss influences cerebral cavernous malformations in miceGwénola Boulday, Noemi Rudini, Luigi Maddaluno, et al.Neurology|October 19, 2012
PRRT2 mutations cause hemiplegic migraineFlorence Riant, Emmanuel Roze, Cecile Barbance, et al.Epilepsia|June 22, 2010
Familial form of typical childhood absence epilepsy in a consanguineous contextHanen Abouda, Yosr Hizem, Amina Gargouri, et al.Pageof 12