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Kai Eriksson

Showing results (31-40 of 39) with videos related to

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European Journal of Human Genetics : EJHG|September 28, 2006
Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patientsTarja Joensuu, Mervi Kuronen, Kirsi Alakurtti, et al.
Epilepsia|July 2, 2013
Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findingsEija Gaily, Anna-Kaisa Anttonen, Leena Valanne, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 26, 2010
[Update on current care guidelines. The treatment of status epilepticus]Reetta Kälviäinen, Kai Eriksson, Olli Häppölä, et al.
European Journal of Human Genetics : EJHG|November 1, 2007
An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseasesColm T O'Dushlaine, Ciara Dolan, Michael E Weale, et al.
Epilepsia|September 27, 2018
Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsyJohanna Hynynen, Tytti Pokka, Jonna Komulainen-Ebrahim, et al.
Epilepsia|July 10, 2002
Visual field constriction in 91 Finnish children treated with vigabatrinSampsa Vanhatalo, Iiris Nousiainen, Kai Eriksson, et al.
Epilepsia Open|November 9, 2024
Epilepsy care pathway: The Finnish modelReetta Kälviäinen, Zakarya Hadj-Allal, Jarkko Kirjavainen, et al.
The Lancet. Neurology|October 5, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control studyGianpiero L Cavalleri, Michael E Weale, Kevin V Shianna, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
European Journal of Human Genetics : EJHG|September 28, 2006
Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patientsTarja Joensuu, Mervi Kuronen, Kirsi Alakurtti, et al.
Epilepsia|July 2, 2013
Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findingsEija Gaily, Anna-Kaisa Anttonen, Leena Valanne, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 26, 2010
[Update on current care guidelines. The treatment of status epilepticus]Reetta Kälviäinen, Kai Eriksson, Olli Häppölä, et al.
European Journal of Human Genetics : EJHG|November 1, 2007
An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseasesColm T O'Dushlaine, Ciara Dolan, Michael E Weale, et al.
Epilepsia|September 27, 2018
Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsyJohanna Hynynen, Tytti Pokka, Jonna Komulainen-Ebrahim, et al.
Epilepsia|July 10, 2002
Visual field constriction in 91 Finnish children treated with vigabatrinSampsa Vanhatalo, Iiris Nousiainen, Kai Eriksson, et al.
Epilepsia Open|November 9, 2024
Epilepsy care pathway: The Finnish modelReetta Kälviäinen, Zakarya Hadj-Allal, Jarkko Kirjavainen, et al.
The Lancet. Neurology|October 5, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control studyGianpiero L Cavalleri, Michael E Weale, Kevin V Shianna, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Pageof 4