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Molecular Genetics and Metabolism Reports|January 9, 2023
Challenges of managing ornithine transcarbamylase deficiency in female heterozygotesAnnette FeigenbaumEuropean Journal of Medical Genetics|October 26, 2010
Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosumAlice Abdel Aleem, Nourhan Abu-Shahba, Dominika Swistun, et al.Neuroimaging Clinics of North America|June 9, 2004
A neuroimaging approach to inborn errors of metabolismSusan Blaser, Annette FeigenbaumDevelopmental Cell|January 18, 2020
Primary Cilia and Brain Wiring, Connecting the DotsQiong Song, Joseph G GleesonPediatric Neurology|September 19, 2003
Is mental retardation a defect of synapse structure and function?Magdalena Chechlacz, Joseph G GleesonTrends in Genetics : TIG|November 13, 2007
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephalyGeraldine Kerjan, Joseph G GleesonNeuron|April 17, 2025
Prefrontal cortex modulation of stress by primary ciliaShixiong Tian, Joseph G GleesonTrends in Neurosciences|May 20, 2020
Closing in on Mechanisms of Open Neural Tube DefectsSangmoon Lee, Joseph G GleesonDevelopmental Medicine and Child Neurology|June 18, 2011
The ciliopathies in neuronal development: a clinical approach to investigation of Joubert syndrome and Joubert syndrome-related disordersShifteh Sattar, Joseph G GleesonNeuron|October 31, 2009
Sun proteins enlighten nuclear movement in developmentHiroyuki Koizumi, Joseph G GleesonPageof 44