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Joseph G Gleeson

Showing results (61-70 of 324) with videos related to

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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.
Neurology|August 17, 2012
Mild paroxysmal kinesigenic dyskinesia caused by PRRT2 missense mutation with reduced penetranceJennifer Friedman, Jesus Olvera, Jennifer L Silhavy, 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.
The Turkish Journal of Pediatrics|December 25, 2015
TSEN54 gene-related pontocerebellar hypoplasia type 2 presenting with exaggerated startle response: report of two cases in a familyHülya Maraş-Genç, Emek Uyur-Yalçın, Rasim Özgür Rosti, et al.
Nature Neuroscience|May 16, 2006
Doublecortin maintains bipolar shape and nuclear translocation during migration in the adult forebrainHiroyuki Koizumi, Holden Higginbotham, Tiffany Poon, et al.
Pageof 33

Showing results (61-70 of 324) with videos related to

Sort By:
Pageof 33
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.
Neurology|August 17, 2012
Mild paroxysmal kinesigenic dyskinesia caused by PRRT2 missense mutation with reduced penetranceJennifer Friedman, Jesus Olvera, Jennifer L Silhavy, 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.
The Turkish Journal of Pediatrics|December 25, 2015
TSEN54 gene-related pontocerebellar hypoplasia type 2 presenting with exaggerated startle response: report of two cases in a familyHülya Maraş-Genç, Emek Uyur-Yalçın, Rasim Özgür Rosti, et al.
Nature Neuroscience|May 16, 2006
Doublecortin maintains bipolar shape and nuclear translocation during migration in the adult forebrainHiroyuki Koizumi, Holden Higginbotham, Tiffany Poon, et al.
Pageof 33