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Stroke|March 20, 2014
Cerebral cavernous malformations arise independent of the heart of glass receptorXiangjian Zheng, Florence Riant, Françoise Bergametti, et al.
Journal of Medical Genetics|April 20, 2023
Biallelic NPR1 loss of function variants are responsible for neonatal systemic hypertensionYline Capri, Theresa Kwon, Olivia Boyer, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|October 18, 2022
Phenotypic variability in 446 CADASIL patients: Impact of NOTCH3 gene mutation location in addition to the effects of age, sex and vascular risk factorsCharlotte Dupé, Stéphanie Guey, Lucie Biard, et al.
European Stroke Journal|April 6, 2023
European Stroke Organisation (ESO) Guidelines on Moyamoya angiopathy Endorsed by Vascular European Reference Network (VASCERN)Anna Bersano, Nadia Khan, Blanca Fuentes, et al.
European Journal of Human Genetics : EJHG|June 22, 2017
Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in CaucasiansStéphanie Guey, Markus Kraemer, Dominique Hervé, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|November 25, 2024
Input of exome sequencing in early-onset cerebral amyloid angiopathyLou Grangeon, Camille Charbonnier, Stéphane Rousseau, et al.
Bioinformatics (Oxford, England)|November 1, 2016
Network-based analysis of omics data: the LEAN methodFrederik Gwinner, Gwénola Boulday, Claire Vandiedonck, et al.
Genes & Development|November 17, 2004
Notch3 is required for arterial identity and maturation of vascular smooth muscle cellsValérie Domenga, Peggy Fardoux, Pierre Lacombe, et al.
Stroke|March 26, 2019
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya AngiopathyLou Grangeon, Stéphanie Guey, Jan Claudius Schwitalla, et al.
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