Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B Ben-Zeev

Showing results (21-30 of 37) with videos related to

Pageof 4
Sort By:
Neurology|April 8, 2009
The common BDNF polymorphism may be a modifier of disease severity in Rett syndromeB Ben Zeev, A Bebbington, G Ho, et al.
Journal of Medical Genetics|February 5, 2002
A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cystsY Shinar, B Ben-Zeev, N Brand, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 7, 2015
The neuropsychological profile of patients with 3-methylglutaconic aciduria type III, Costeff syndromeS Sofer, A Schweiger, L Blumkin, et al.
Neurogenetics|February 26, 2009
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypesS Russo, M Marchi, F Cogliati, et al.
European Journal of Neurology|April 8, 2009
Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrinS Cohen-Sadan, U Kramer, B Ben-Zeev, et al.
American Journal of Medical Genetics|October 1, 1994
Familial Dandy-Walker malformation associated with macrocephaly, facial anomalies, developmental delay, and brain stem dysgenesis: prenatal diagnosis and postnatal outcome in brothers. A new syndrome?D Chitayat, L Moore, M R Del Bigio, et al.
Neurology|February 26, 2003
Malformations of cortical development with balloon cells: clinical and radiologic correlatesM T Mackay, L E Becker, S H Chuang, et al.
Journal of Neurology|August 25, 1999
Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxiaS Hassin-Baer, A Bar-Shira, S Gilad, et al.
Neurology|March 12, 2008
Investigating genotype-phenotype relationships in Rett syndrome using an international data setA Bebbington, A Anderson, D Ravine, et al.
Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Neurology|April 8, 2009
The common BDNF polymorphism may be a modifier of disease severity in Rett syndromeB Ben Zeev, A Bebbington, G Ho, et al.
Journal of Medical Genetics|February 5, 2002
A common ancestral haplotype in carrier chromosomes from different ethnic backgrounds in vacuolating megalencephalic leucoencephalopathy with subcortical cystsY Shinar, B Ben-Zeev, N Brand, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 7, 2015
The neuropsychological profile of patients with 3-methylglutaconic aciduria type III, Costeff syndromeS Sofer, A Schweiger, L Blumkin, et al.
Neurogenetics|February 26, 2009
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypesS Russo, M Marchi, F Cogliati, et al.
European Journal of Neurology|April 8, 2009
Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrinS Cohen-Sadan, U Kramer, B Ben-Zeev, et al.
American Journal of Medical Genetics|October 1, 1994
Familial Dandy-Walker malformation associated with macrocephaly, facial anomalies, developmental delay, and brain stem dysgenesis: prenatal diagnosis and postnatal outcome in brothers. A new syndrome?D Chitayat, L Moore, M R Del Bigio, et al.
Neurology|February 26, 2003
Malformations of cortical development with balloon cells: clinical and radiologic correlatesM T Mackay, L E Becker, S H Chuang, et al.
Journal of Neurology|August 25, 1999
Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxiaS Hassin-Baer, A Bar-Shira, S Gilad, et al.
Neurology|March 12, 2008
Investigating genotype-phenotype relationships in Rett syndrome using an international data setA Bebbington, A Anderson, D Ravine, et al.
Journal of Medical Genetics|November 17, 2009
Updating the profile of C-terminal MECP2 deletions in Rett syndromeA Bebbington, A Percy, J Christodoulou, et al.
Pageof 4