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Journal of Child Neurology|April 26, 2012
The very low density lipoprotein receptor-associated pontocerebellar hypoplasia and dysmorphic features in three Turkish patientsFatma Mujgan Sonmez, Joseph G Gleeson, Figen Celep, et al.Biological Psychiatry|February 9, 2023
Stem Cell-Based Organoid Models of Neurodevelopmental DisordersLu Wang, Charlotte Owusu-Hammond, David Sievert, et al.Current Protocols|June 8, 2021
Efficient Derivation of Excitatory and Inhibitory Neurons from Human Pluripotent Stem Cells Stably Expressing Direct Reprogramming FactorsSaera Song, Archana Ashok, Damian Williams, et al.Annual Review of Cell and Developmental Biology|October 12, 2004
Cortical neuronal migration mutants suggest separate but intersecting pathwaysStephanie Bielas, Holden Higginbotham, Hiroyuki Koizumi, et al.Nature Reviews. Neurology|December 4, 2013
Primary cilia in neurodevelopmental disordersEnza Maria Valente, Rasim O Rosti, Elizabeth Gibbs, et al.American Journal of Medical Genetics. Part A|October 18, 2011
Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiersMaha S Zaki, Shifteh Sattar, Rustin A Massoudi, et al.American Journal of Medical Genetics. Part A|July 18, 2009
Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorderMaha S Zaki, Hanan H Afifi, A J Barkovich, et al.Developmental Medicine and Child Neurology|October 15, 2013
The genetic landscape of autism spectrum disordersRasim O Rosti, Abdelrahim A Sadek, Keith K Vaux, et al.Current Opinion in Neurology|March 2, 2013
Hemimegalencephaly, a paradigm for somatic postzygotic neurodevelopmental disordersSeung Tae Baek, Elizabeth M Gibbs, Joseph G Gleeson, et al.American Journal of Medical Genetics. Part A|June 26, 2015
Dandy-Walker malformation, genitourinary abnormalities, and intellectual disability in two familiesMaha S Zaki, Amira Masri, Anne Gregor, et al.Pageof 31