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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
November 18, 2003
[Hereditary cerebral arteriopathy]
W Rein Gustavsen, Kristin Eiklid
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
May 11, 2010
[Determination of chromosome aberrations with the help of DNA arrays]
Olaug K Rødningen, Trine E Prescott, Randi Hovland, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
July 9, 2010
Fanconi anaemia, BRCA2 and familial considerations - follow up on a previous case report
Trine Levin Bodd, Marijke Van Ghelue, Kristin Eiklid, et al.
Frontiers in Neurology
|
March 7, 2022
APOE-ε4 Is Associated With Reduced Verbal Memory Performance and Higher Emotional, Cognitive, and Everyday Executive Function Symptoms Two Months After Mild Traumatic Brain Injury
Torgeir Hellstrøm, Nada Andelic, Øyvor Øistensen Holthe, et al.
Journal of Clinical Medicine
|
January 27, 2021
Apolipoprotein ɛ4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging
Torgeir Hellstrøm, Nada Andelic, Ann-Marie G de Lange, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
November 21, 2008
ABCB4 sequence variations in young adults with cholesterol gallstone disease
Karl Esten Nakken, Knut Jørgen Labori, Olaug K Rødningen, et al.
Respiratory Medicine
|
May 9, 2006
CFTR gene mutations and asthma in the Norwegian Environment and Childhood Asthma study
Monica Cheng Munthe-Kaas, Karin C Lødrup Carlsen, Kai-Håkon Carlsen, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2005
Novel splicing mutation in the NEMO (IKK-gamma) gene with severe immunodeficiency and heterogeneity of X-chromosome inactivation
Karen Helene Ørstavik, Marianne Kristiansen, Gun Peggy Knudsen, et al.
Plos One
|
October 3, 2013
CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops
Sohela Shah, Laura K Conlin, Luis Gomez, et al.
The Journal of Pediatrics
|
April 25, 2003
Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome
Martin Frühwirth, Andreas R Janecke, Thomas Müller, et al.
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
November 18, 2003
[Hereditary cerebral arteriopathy]
W Rein Gustavsen, Kristin Eiklid
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
May 11, 2010
[Determination of chromosome aberrations with the help of DNA arrays]
Olaug K Rødningen, Trine E Prescott, Randi Hovland, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
July 9, 2010
Fanconi anaemia, BRCA2 and familial considerations - follow up on a previous case report
Trine Levin Bodd, Marijke Van Ghelue, Kristin Eiklid, et al.
Frontiers in Neurology
|
March 7, 2022
APOE-ε4 Is Associated With Reduced Verbal Memory Performance and Higher Emotional, Cognitive, and Everyday Executive Function Symptoms Two Months After Mild Traumatic Brain Injury
Torgeir Hellstrøm, Nada Andelic, Øyvor Øistensen Holthe, et al.
Journal of Clinical Medicine
|
January 27, 2021
Apolipoprotein ɛ4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging
Torgeir Hellstrøm, Nada Andelic, Ann-Marie G de Lange, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
November 21, 2008
ABCB4 sequence variations in young adults with cholesterol gallstone disease
Karl Esten Nakken, Knut Jørgen Labori, Olaug K Rødningen, et al.
Respiratory Medicine
|
May 9, 2006
CFTR gene mutations and asthma in the Norwegian Environment and Childhood Asthma study
Monica Cheng Munthe-Kaas, Karin C Lødrup Carlsen, Kai-Håkon Carlsen, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2005
Novel splicing mutation in the NEMO (IKK-gamma) gene with severe immunodeficiency and heterogeneity of X-chromosome inactivation
Karen Helene Ørstavik, Marianne Kristiansen, Gun Peggy Knudsen, et al.
Plos One
|
October 3, 2013
CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops
Sohela Shah, Laura K Conlin, Luis Gomez, et al.
The Journal of Pediatrics
|
April 25, 2003
Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome
Martin Frühwirth, Andreas R Janecke, Thomas Müller, et al.
Page
of 2