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Helle Hjalgrim

Showing results (21-30 of 71) with videos related to

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European Journal of Human Genetics : EJHG|June 17, 2004
Screening of the ARX gene in 682 retarded malesKaren Grønskov, Helle Hjalgrim, Inge-Merete Nielsen, et al.
Ugeskrift for Laeger|April 19, 2017
[Dietary treatment of medically refractory epilepsy in children and adolescents]Frederikke Høgsbro-Rode, Katrine M Harris Johannesen, Vibeke Stubbings, et al.
Epilepsia|January 11, 2016
From unwitnessed fatality to witnessed rescue: Nonpharmacologic interventions in sudden unexpected death in epilepsyFergus Rugg-Gunn, John Duncan, Helle Hjalgrim, et al.
European Journal of Human Genetics : EJHG|September 3, 2010
Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsyLaura L Klitten, Rikke S Møller, Kirstine Ravn, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 1, 2019
Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutationsGaetan Lesca, Rikke S Møller, Gabrielle Rudolf, et al.
Epilepsia|November 5, 2011
A balanced translocation disrupts SYNGAP1 in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA)Laura L Klitten, Rikke S Møller, Marina Nikanorova, et al.
Ugeskrift for Laeger|April 27, 2012
[Genetic causes of infantile spasms--a systematic review]Lars Kjærsgaard Hansen, Lilian Bomme Ousager, Rikke Steensbjerre Møller, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 27, 2010
Performance on Wechsler intelligence scales in children with Tourette syndromeNanette M M M Debes, Theis Lange, Tanja L Jessen, et al.
Molecular Cytogenetics|April 23, 2015
Dysregulation of FOXG1 by ring chromosome 14Daniela Alosi, Laura Line Klitten, Mads Bak, et al.
Annals of Neurology|December 30, 2014
Automated differentiation between epileptic and nonepileptic convulsive seizuresSándor Beniczky, Isa Conradsen, Mihai Moldovan, et al.
Pageof 8

Showing results (21-30 of 71) with videos related to

Sort By:
Pageof 8
European Journal of Human Genetics : EJHG|June 17, 2004
Screening of the ARX gene in 682 retarded malesKaren Grønskov, Helle Hjalgrim, Inge-Merete Nielsen, et al.
Ugeskrift for Laeger|April 19, 2017
[Dietary treatment of medically refractory epilepsy in children and adolescents]Frederikke Høgsbro-Rode, Katrine M Harris Johannesen, Vibeke Stubbings, et al.
Epilepsia|January 11, 2016
From unwitnessed fatality to witnessed rescue: Nonpharmacologic interventions in sudden unexpected death in epilepsyFergus Rugg-Gunn, John Duncan, Helle Hjalgrim, et al.
European Journal of Human Genetics : EJHG|September 3, 2010
Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsyLaura L Klitten, Rikke S Møller, Kirstine Ravn, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 1, 2019
Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutationsGaetan Lesca, Rikke S Møller, Gabrielle Rudolf, et al.
Epilepsia|November 5, 2011
A balanced translocation disrupts SYNGAP1 in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA)Laura L Klitten, Rikke S Møller, Marina Nikanorova, et al.
Ugeskrift for Laeger|April 27, 2012
[Genetic causes of infantile spasms--a systematic review]Lars Kjærsgaard Hansen, Lilian Bomme Ousager, Rikke Steensbjerre Møller, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 27, 2010
Performance on Wechsler intelligence scales in children with Tourette syndromeNanette M M M Debes, Theis Lange, Tanja L Jessen, et al.
Molecular Cytogenetics|April 23, 2015
Dysregulation of FOXG1 by ring chromosome 14Daniela Alosi, Laura Line Klitten, Mads Bak, et al.
Annals of Neurology|December 30, 2014
Automated differentiation between epileptic and nonepileptic convulsive seizuresSándor Beniczky, Isa Conradsen, Mihai Moldovan, et al.
Pageof 8