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

Helle Hjalgrim

Showing results (31-40 of 71) with videos related to

Pageof 8
Sort By:
Annales De Genetique|June 24, 2003
Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunctionCíntia Barros Santos, Helle Hjalgrim, Flávia Raquel Gonçalves Carneiro, et al.
Epilepsia|June 4, 2014
Quantitative analysis of surface electromyography during epileptic and nonepileptic convulsive seizuresSándor Beniczky, Isa Conradsen, Mihai Moldovan, et al.
Epilepsy Research|September 3, 2011
Transcranial direct current stimulation in refractory continuous spikes and waves during slow sleep: a controlled studyEdina T Varga, Daniella Terney, Mary D Atkins, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 17, 2012
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersLinh Duong, Laura L Klitten, Rikke S Møller, et al.
BMC Medical Genetics|May 21, 2005
Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qterMarie Sogaard, Zeynep Tümer, Helle Hjalgrim, et al.
Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.
Journal of Child Neurology|October 12, 2013
Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsiesAnna Baumgart, Sarah von Spiczak, Nanda M Verhoeven-Duif, et al.
Annals of Neurology|April 22, 2016
ReplyElena Gardella, Sándor Beniczky, Rikke S Møller, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsyMai-Britt Mosbech, Anne S B Olsen, Ditte Neess, et al.
American Journal of Human Genetics|January 17, 2003
Expansion of the fragile X CGG repeat in females with premutation or intermediate allelesSarah L Nolin, W Ted Brown, Anne Glicksman, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Annales De Genetique|June 24, 2003
Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunctionCíntia Barros Santos, Helle Hjalgrim, Flávia Raquel Gonçalves Carneiro, et al.
Epilepsia|June 4, 2014
Quantitative analysis of surface electromyography during epileptic and nonepileptic convulsive seizuresSándor Beniczky, Isa Conradsen, Mihai Moldovan, et al.
Epilepsy Research|September 3, 2011
Transcranial direct current stimulation in refractory continuous spikes and waves during slow sleep: a controlled studyEdina T Varga, Daniella Terney, Mary D Atkins, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 17, 2012
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersLinh Duong, Laura L Klitten, Rikke S Møller, et al.
BMC Medical Genetics|May 21, 2005
Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qterMarie Sogaard, Zeynep Tümer, Helle Hjalgrim, et al.
Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.
Journal of Child Neurology|October 12, 2013
Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsiesAnna Baumgart, Sarah von Spiczak, Nanda M Verhoeven-Duif, et al.
Annals of Neurology|April 22, 2016
ReplyElena Gardella, Sándor Beniczky, Rikke S Møller, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsyMai-Britt Mosbech, Anne S B Olsen, Ditte Neess, et al.
American Journal of Human Genetics|January 17, 2003
Expansion of the fragile X CGG repeat in females with premutation or intermediate allelesSarah L Nolin, W Ted Brown, Anne Glicksman, et al.
Pageof 8