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Journal of Alzheimer'S Disease : JAD
|
April 24, 2010
Converging pathways of chromogranin and amyloid metabolism in the brain
Niklas 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 sclerosis
Christina 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 damage
Daniel 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 diseases
Lucinda 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 pairs
Annette 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 COL4A1
Maija 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 pathogenesis
Jesse Huang, Katarina Tengvall, Izaura Bomfim Lima, et al.
Journal of Neuroimmunology
|
October 25, 2003
Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patients
Hanne 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 sclerosis
Viktor 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 deficiency
Rikke K J Olsen, Simon E Olpin, Brage S Andresen, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Journal of Alzheimer'S Disease : JAD
|
April 24, 2010
Converging pathways of chromogranin and amyloid metabolism in the brain
Niklas 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 sclerosis
Christina 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 damage
Daniel 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 diseases
Lucinda 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 pairs
Annette 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 COL4A1
Maija 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 pathogenesis
Jesse Huang, Katarina Tengvall, Izaura Bomfim Lima, et al.
Journal of Neuroimmunology
|
October 25, 2003
Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patients
Hanne 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 sclerosis
Viktor 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 deficiency
Rikke K J Olsen, Simon E Olpin, Brage S Andresen, et al.
Page
of 7