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Biological Psychiatry|February 9, 2023
Stem Cell-Based Organoid Models of Neurodevelopmental DisordersLu Wang, Charlotte Owusu-Hammond, David Sievert, 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.Journal of Child Neurology|December 21, 2004
Autism in several members of a family with generalized epilepsy with febrile seizures plusTracy J Dixon-Salazar, Lesley C Keeler, Doris A Trauner, et al.Journal of Child Neurology|August 4, 2012
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome: a case reportAriana Kariminejad, Farid Radmanesh, Ali-Reza Rezayi, et al.Pageof 33