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European Journal of Human Genetics : EJHG|January 19, 2006
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndromeElisabeth Lajeunie, Solange Heuertz, Vincent El Ghouzzi, et al.
Traffic (Copenhagen, Denmark)|May 25, 2007
Activated somatostatin type 2 receptors traffic in vivo in central neurons from dendrites to the trans Golgi before recyclingZsolt Csaba, Benjamin Lelouvier, Cécile Viollet, et al.
Annals of Neurology|December 14, 2011
Stem cell therapy for neonatal brain injury: perspectives and challengesLuigi Titomanlio, Annemieke Kavelaars, Jeremie Dalous, et al.
Human Mutation|October 9, 2012
A novel RAB33B mutation in Smith-McCort dysplasiaNina Dupuis, Sophie Lebon, Manoj Kumar, et al.
Annals of Clinical and Translational Neurology|January 10, 2015
Endogenous cerebellar neurogenesis in adult mice with progressive ataxiaManoj Kumar, Zsolt Csaba, Stéphane Peineau, et al.
Iscience|March 9, 2026
Oropouche virus infects human neural progenitor cells and alters the growth of brain organoidsAlexandra Albert, Laurine Couture, François Piumi, et al.
Journal of Neuropathology and Experimental Neurology|September 7, 2007
Apoptosis-inducing factor deficiency induces early mitochondrial degeneration in brain followed by progressive multifocal neuropathologyVincent El Ghouzzi, Zsolt Csaba, Paul Olivier, et al.
Developmental Medicine and Child Neurology|June 21, 2022
Neurological outcome in WDR62 primary microcephalyLyse Ruaud, Séverine Drunat, Monique Elmaleh-Bergès, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 17, 2008
Vulnerability of white matter towards antenatal hypoxia is linked to a species-dependent regulation of glutamate receptor subunitsRomain H Fontaine, Paul Olivier, Véronique Massonneau, et al.
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