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Neuropathology and Applied Neurobiology
|
January 1, 1984
Immunohistochemical demonstration of amyloid P component in cerebro-vascular amyloidosis
I 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 amyloidosis
J 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 Syndrome
Sigridur 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 function
H 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 leukaemia
H 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 amyloidosis
H 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 family
G E Moore, R Williamson, O Jensson, et al.
Stroke
|
July 1, 1996
Immune reactions associated with cerebral amyloid angiopathy
M 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 family
F 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 defects
R Newton, P Stanier, S Loughna, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 102) with videos related to
Sort By:
Page
of 11
Neuropathology and Applied Neurobiology
|
January 1, 1984
Immunohistochemical demonstration of amyloid P component in cerebro-vascular amyloidosis
I 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 amyloidosis
J 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 Syndrome
Sigridur 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 function
H 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 leukaemia
H 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 amyloidosis
H 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 family
G E Moore, R Williamson, O Jensson, et al.
Stroke
|
July 1, 1996
Immune reactions associated with cerebral amyloid angiopathy
M 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 family
F 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 defects
R Newton, P Stanier, S Loughna, et al.
Page
of 11