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O Jensson

Showing results (51-60 of 102) with videos related to

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Neuropathology and Applied Neurobiology|January 1, 1984
Immunohistochemical demonstration of amyloid P component in cerebro-vascular amyloidosisI F Rowe, O Jensson, P D Lewis, et al.
Acta Neurologica Scandinavica|May 1, 1994
Co-localization of beta/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosisJ Haan, M L Maat-Schieman, S G van Duinen, et al.
Kidney International Reports|May 14, 2023
Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic SyndromeSigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Brynjar O Jensson, et al.
Scandinavian Journal of Immunology|August 1, 1994
Familial macroglobulinaemia: hyperactive B-cells but normal natural killer functionH M Ogmundsdóttir, G M Jóhannesson, S Sveinsdóttir, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|January 1, 1992
Natural killer cell function and malignant cell phenotype in hairy cell leukaemiaH M Ogmundsdóttir, L Thorsteinsson, A Sigfússon, et al.
Stroke|March 1, 1987
Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosisH Löfberg, A O Grubb, E K Nilsson, et al.
Journal of Craniofacial Genetics and Developmental Biology|October 1, 1991
Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic familyG E Moore, R Williamson, O Jensson, et al.
Stroke|July 1, 1996
Immune reactions associated with cerebral amyloid angiopathyM Yamada, Y Itoh, M Shintaku, et al.
Human Genetics|April 1, 1994
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic familyF A Hol, M P Geurds, O Jensson, et al.
Clinical Genetics|May 1, 1994
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defectsR Newton, P Stanier, S Loughna, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
Neuropathology and Applied Neurobiology|January 1, 1984
Immunohistochemical demonstration of amyloid P component in cerebro-vascular amyloidosisI F Rowe, O Jensson, P D Lewis, et al.
Acta Neurologica Scandinavica|May 1, 1994
Co-localization of beta/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosisJ Haan, M L Maat-Schieman, S G van Duinen, et al.
Kidney International Reports|May 14, 2023
Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic SyndromeSigridur Sunna Aradottir, Ann-Charlotte Kristoffersson, Brynjar O Jensson, et al.
Scandinavian Journal of Immunology|August 1, 1994
Familial macroglobulinaemia: hyperactive B-cells but normal natural killer functionH M Ogmundsdóttir, G M Jóhannesson, S Sveinsdóttir, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|January 1, 1992
Natural killer cell function and malignant cell phenotype in hairy cell leukaemiaH M Ogmundsdóttir, L Thorsteinsson, A Sigfússon, et al.
Stroke|March 1, 1987
Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosisH Löfberg, A O Grubb, E K Nilsson, et al.
Journal of Craniofacial Genetics and Developmental Biology|October 1, 1991
Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic familyG E Moore, R Williamson, O Jensson, et al.
Stroke|July 1, 1996
Immune reactions associated with cerebral amyloid angiopathyM Yamada, Y Itoh, M Shintaku, et al.
Human Genetics|April 1, 1994
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic familyF A Hol, M P Geurds, O Jensson, et al.
Clinical Genetics|May 1, 1994
Linkage analysis of 62 X-chromosomal loci excludes the X chromosome in an Icelandic family showing apparent X-linked recessive inheritance of neural tube defectsR Newton, P Stanier, S Loughna, et al.
Pageof 11