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Kaja Kristine Selmer

Showing results (1-10 of 34) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 11, 2011
[Glucose transporter protein type 1 (GLUT-1) deficiency syndrome]Anette Ramm-Pettersen, Kaja Kristine Selmer, Karl O Nakken
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 24, 2019
Pyruvate dehydrogenase deficiencySigrid Pedersen, Yngve Thomas Bliksrud, Kaja Kristine Selmer, et al.
Acta Ophthalmologica|August 21, 2019
Inherited retinal disease in Norway - a characterization of current clinical and genetic knowledgeJosephine Prener Holtan, Kaja Kristine Selmer, Ketil Riddervold Heimdal, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 10, 2012
[Juvenile myoclonic epilepsy]Marte Roa Syvertsen, Rune Markhus, Kaja Kristine Selmer, et al.
Epilepsy & Behavior : E&B|March 12, 2014
CHD2 mutations in Lennox-Gastaut syndromeCaroline Lund, Eylert Brodtkorb, Ane-Marte Øye, et al.
Epilepsy & Behavior : E&B|September 21, 2014
Does ketogenic diet improve cognitive function in patients with GLUT1-DS? A 6- to 17-month follow-up studyAnette Ramm-Pettersen, Kirsten Engberg Stabell, Karl O Nakken, et al.
Epilepsy Research|February 19, 2013
Copy number variants in adult patients with Lennox-Gastaut syndrome featuresCaroline Lund, Eylert Brodtkorb, Oddveig Røsby, et al.
Epilepsy & Behavior : E&B|February 11, 2014
Occurrence of GLUT1 deficiency syndrome in patients treated with ketogenic dietAnette Ramm-Pettersen, Karl O Nakken, Kathrine Cammermeyer Haavardsholm, et al.
Epilepsy & Behavior : E&B|April 14, 2017
GLUT1-deficiency syndrome: Report of a four-generation Norwegian family with a mild phenotypeAnette Ramm-Pettersen, Karl O Nakken, Kathrine C Haavardsholm, et al.
Epilepsy & Behavior : E&B|September 29, 2009
SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome featuresKaja Kristine Selmer, Caroline Lund, Kristin Brandal, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 11, 2011
[Glucose transporter protein type 1 (GLUT-1) deficiency syndrome]Anette Ramm-Pettersen, Kaja Kristine Selmer, Karl O Nakken
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|October 24, 2019
Pyruvate dehydrogenase deficiencySigrid Pedersen, Yngve Thomas Bliksrud, Kaja Kristine Selmer, et al.
Acta Ophthalmologica|August 21, 2019
Inherited retinal disease in Norway - a characterization of current clinical and genetic knowledgeJosephine Prener Holtan, Kaja Kristine Selmer, Ketil Riddervold Heimdal, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|August 10, 2012
[Juvenile myoclonic epilepsy]Marte Roa Syvertsen, Rune Markhus, Kaja Kristine Selmer, et al.
Epilepsy & Behavior : E&B|March 12, 2014
CHD2 mutations in Lennox-Gastaut syndromeCaroline Lund, Eylert Brodtkorb, Ane-Marte Øye, et al.
Epilepsy & Behavior : E&B|September 21, 2014
Does ketogenic diet improve cognitive function in patients with GLUT1-DS? A 6- to 17-month follow-up studyAnette Ramm-Pettersen, Kirsten Engberg Stabell, Karl O Nakken, et al.
Epilepsy Research|February 19, 2013
Copy number variants in adult patients with Lennox-Gastaut syndrome featuresCaroline Lund, Eylert Brodtkorb, Oddveig Røsby, et al.
Epilepsy & Behavior : E&B|February 11, 2014
Occurrence of GLUT1 deficiency syndrome in patients treated with ketogenic dietAnette Ramm-Pettersen, Karl O Nakken, Kathrine Cammermeyer Haavardsholm, et al.
Epilepsy & Behavior : E&B|April 14, 2017
GLUT1-deficiency syndrome: Report of a four-generation Norwegian family with a mild phenotypeAnette Ramm-Pettersen, Karl O Nakken, Kathrine C Haavardsholm, et al.
Epilepsy & Behavior : E&B|September 29, 2009
SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome featuresKaja Kristine Selmer, Caroline Lund, Kristin Brandal, et al.
Pageof 4