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Oluf Andersen

Showing results (51-60 of 63) with videos related to

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Journal of Alzheimer'S Disease : JAD|April 24, 2010
Converging pathways of chromogranin and amyloid metabolism in the brainNiklas Mattsson, Per Johansson, Oskar Hansson, et al.
European Journal of Neurology|October 15, 2014
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosisChristina Sundal, Matt Baker, Virginija Karrenbauer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 6, 2023
Seroreactivity against lytic, latent and possible cross-reactive EBV antigens appears on average 10 years before MS induced preclinical neuroaxonal damageDaniel Jons, Viktor Grut, Tomas Bergström, et al.
Brain Pathology (Zurich, Switzerland)|February 8, 2013
Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseasesLucinda J L Craggs, Christian Hagel, Gregor Kuhlenbaeumer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 6, 2004
Concordance for disease course and age of onset in Scandinavian multiple sclerosis coaffected sib pairsAnnette Bang Oturai, Lars P Ryder, Sten Fredrikson, et al.
Brain : a Journal of Neurology|April 4, 2017
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, et al.
Brain : a Journal of Neurology|April 17, 2024
Genetics of immune response to Epstein-Barr virus: prospects for multiple sclerosis pathogenesisJesse Huang, Katarina Tengvall, Izaura Bomfim Lima, et al.
Journal of Neuroimmunology|October 25, 2003
Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patientsHanne F Harbo, Pameli Datta, Annette Oturai, et al.
Brain : a Journal of Neurology|November 6, 2023
Human herpesvirus 6A and axonal injury before the clinical onset of multiple sclerosisViktor Grut, Martin Biström, Jonatan Salzer, et al.
Brain : a Journal of Neurology|June 23, 2007
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Simon E Olpin, Brage S Andresen, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Journal of Alzheimer'S Disease : JAD|April 24, 2010
Converging pathways of chromogranin and amyloid metabolism in the brainNiklas Mattsson, Per Johansson, Oskar Hansson, et al.
European Journal of Neurology|October 15, 2014
Hereditary diffuse leukoencephalopathy with spheroids with phenotype of primary progressive multiple sclerosisChristina Sundal, Matt Baker, Virginija Karrenbauer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 6, 2023
Seroreactivity against lytic, latent and possible cross-reactive EBV antigens appears on average 10 years before MS induced preclinical neuroaxonal damageDaniel Jons, Viktor Grut, Tomas Bergström, et al.
Brain Pathology (Zurich, Switzerland)|February 8, 2013
Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseasesLucinda J L Craggs, Christian Hagel, Gregor Kuhlenbaeumer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 6, 2004
Concordance for disease course and age of onset in Scandinavian multiple sclerosis coaffected sib pairsAnnette Bang Oturai, Lars P Ryder, Sten Fredrikson, et al.
Brain : a Journal of Neurology|April 4, 2017
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, et al.
Brain : a Journal of Neurology|April 17, 2024
Genetics of immune response to Epstein-Barr virus: prospects for multiple sclerosis pathogenesisJesse Huang, Katarina Tengvall, Izaura Bomfim Lima, et al.
Journal of Neuroimmunology|October 25, 2003
Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patientsHanne F Harbo, Pameli Datta, Annette Oturai, et al.
Brain : a Journal of Neurology|November 6, 2023
Human herpesvirus 6A and axonal injury before the clinical onset of multiple sclerosisViktor Grut, Martin Biström, Jonatan Salzer, et al.
Brain : a Journal of Neurology|June 23, 2007
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Simon E Olpin, Brage S Andresen, et al.
Pageof 7