Ó. Jensson

发表

Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresis

B. Levinson, J. Gitschier, S. Jónsdóttir, 1992, Human mutation.

Mutation in the cystatin C gene causes hereditary brain hemorrhage.

I. Olafsson, M. Abrahamson, Ó. Jensson, 1989, Progress in clinical and biological research.

The Molecular Pathology of Hereditary Cystatin C Amyloid Angiopathy Causing Brain Hemorrhage

I. Olafsson, Ó. Jensson, L. Thorsteinsson, 1996, Brain pathology.

Structure and expression of the human cystatin C gene.

I. Olafsson, M. Abrahamson, Ó. Jensson, 1990, The Biochemical journal.

MUTATION IN CYSTATIN C GENE CAUSES HEREDITARY BRAIN HAEMORRHAGE

I. Olafsson, M. Abrahamson, Ó. Jensson, 1988, The Lancet.

Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage.

G. Gudmundsson, B. Frangione, Ó. Jensson, 1987, Acta neurologica Scandinavica.

Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosis.

G. Gudmundsson, Ó. Jensson, A. Grubb, 1984, The New England journal of medicine.

Co‐localization of β/A4 and cystatin C in cortical blood vessels in Dutch, but not in Icelandic hereditary cerebral hemorrhage with amyloidosis

R. Roos, S. Duinen, Ó. Jensson, 1994, Acta neurologica Scandinavica.

The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms.

I. Olafsson, G. Gudmundsson, M. Abrahamson, 1990, Scandinavian journal of clinical and laboratory investigation.

Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace

B. Frangione, Ó. Jensson, H. Feiner, 1983, The Journal of experimental medicine.

Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the brain

H. Vinters, Ó. Jensson, L. Thorsteinsson, 1997, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C).

J. Ghiso, B. Frangione, Ó. Jensson, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Gc subtypes in Icelanders.

Ó. Jensson, A. Árnason, I. Skaftadottir, 1983, Human heredity.

Macroglobulinaemia in an Icelandic family.

Ó. Jensson, Ó. Björnsson, A. Árnason, 2009, Acta medica Scandinavica.

Immune reactions associated with cerebral amyloid angiopathy.

M. Yamada, E. Otomo, Y. Itoh, 1996, Stroke.

Gene organization of haplotypes expressing two different C4A allotypes

R. Fossdal, Ó. Jensson, A. Palsdottir, 1987, Human Genetics.

Heterogeneity of human C4 gene size

R. Fossdal, J. Edwards, Ó. Jensson, 1987, Immunogenetics.

Wilson disease in Iceland: a clinical and genetic study.

G. Gudmundsson, D. Cox, Ó. Jensson, 1995, American journal of human genetics.

Gc subtypes in Northern Indians.

Ó. Jensson, A. Árnason, P. Mackintosh, 1983, Human heredity.

Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosis.

G. Gudmundsson, E. Nilsson, Ó. Jensson, 1987, Stroke.

Cystatin C (γ-Trace) and β-Protein Coexist in the Cerebral Amyloid Angiopathy Causing Cerebral Hemorrhage and Consequential Vascular Dementia

Shotai Kobayashi, Ó. Jensson, Morihiko Nakamura, 1990 .

Absence of the cystatin C amyloid in the cerebral amyloid angiopathy, senile plaque, and extra‐CNS amyloid deposits of aged Japanese

Y. Wada, E. Otomo, H. Tsukagoshi, 1989, Acta Neurologica Scandinavica.

IMMUNOHISTOCHEMICAL DEMONSTRATION OF AMYLOID P COMPONENT IN CEREBRO‐VASCULAR AMYLOIDOSIS

P. D. Lewis, M. Pepys, G. Tennent, 1984, Neuropathology and applied neurobiology.

causing amyloid angiopathy and brain hemorrhage ‐ clinical genetics in Iceland

Ó. Jensson, A. Palsdottir, L. Thorsteinsson, 1989, Clinical genetics.

The First Icelandic Family with X‐Linked Agammaglobulinemia: Studies of Genetic Markers and Immune Function

G. Eyjolfsson, Ó. Jensson, L. Thorsteinsson, 1990, Scandinavian journal of immunology.

Amyloid Fibrils in Hereditary Cerebral Hemorrhage with Amyloidosis (HCHWAS) is Related to Cystatin (Gamma Trace)

B. Frangione, Ó. Jensson, H. Feiner, 1986 .

Human cystatin C expression and regulation by TGF-β1: Implications for the pathogenesis of hereditary cystatin C amyloid angiopathy causing brain hemorrhage

V. Emilsson, Ó. Jensson, L. Thorsteinsson, 1996 .

Observations on the Leucocyte Blood Picture in Acute Uraemia

Ó. Jensson, 1958, British journal of haematology.

Von Willebrand's disease in an Icelandic family.

Ó. Jensson, L. Wallett, 2009, Acta medica Scandinavica.

X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17

A. Ivens, R. Williamson, Ó. Jensson, 1988, Human Genetics.

The application of molecular genetics to detection of craniofacial abnormality.

A. Bjornsson, A. Ivens, R. Williamson, 1988, Development.

ANTI‐TISSUE ANTIBODIES AND IMMUNOGLOBULIN LEVELS IN RELATION TO HLA AND OTHER MARKERS IN ICELANDIC FAMILIES

J. Edwards, Ó. Jensson, D. Stanworth, 1979, Journal of immunogenetics.

Studies on Hereditary Spherocytosis in Iceland

S. Magnússon, Ó. Jensson, J. L. Jónasson, 2009 .

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

M. Farrall, S. Forbes, P. Stanier, 1994, Clinical Genetics.

Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.

A. Ivens, R. Williamson, Ó. Jensson, 1991, Journal of craniofacial genetics and developmental biology.

Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis

I. Olafsson, M. Abrahamson, Ó. Jensson, 1992, Human Genetics.

Hereditary Central Nervous System γ-Trace Amyloid Angiopathy and Stroke in Icelandic Families

G. Gudmundsson, Ó. Jensson, H. Löfberg, 1986 .

Linkage of an X-chromosome cleft palate gene

M. Farrall, A. Ivens, R. Williamson, 1987, Nature.

Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family

E. Mariman, B. Hamel, Ó. Jensson, 1994, Human Genetics.

A family showing apparent X linked inheritance of both anencephaly and spina bifida.

R. Fossdal, Ó. Jensson, S. Hreidarsson, 1988, Journal of medical genetics.

Natural killer cell function and malignant cell phenotype in hairy cell leukaemia

G. Eyjolfsson, Ó. Jensson, S. Sveinsdóttir, 1992, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

Serum amyloid P-component and C-reactive protein in serum of healthy Icelanders and members of an Icelandic family with macroglobulinaemia.

M. Pepys, Ó. Jensson, Ó. Björnsson, 2009, Acta medica Scandinavica.

Familial Macroglobulinaemia: Hyperactive B‐Cells but Normal Natural Killer Function

A. Hegeman, Ó. Jensson, S. Sveinsdóttir, 1994, Scandinavian journal of immunology.

Familial Acute Myeloid Leukaemia with Acquired Pelger-Huët Anomaly and Aneuploidy of C Group

D. Catovsky, H. Valdimarsson, Ó. Jensson, 1972, British medical journal.

An Isolate of Families with Hereditary Cystatin C Amyloid Angiopathy and Cerebral Haemorrhage in the South of Iceland

I. Olafsson, G. Gudmundsson, M. Abrahamson, 1988 .

Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysis

R. Fossdal, M. Breuning, D. Peters, 1993, Human Genetics.

X Chromosome Genes Involved in the Regulation of Facial Clefting and Spina Bifida

A. Ivens, Ó. Jensson, D. Henderson, 1990 .

Perturbation of processing of cystatin C in monocytes from patients with hereditary cystatin C amyloid angiopathy

I. Olafsson, B. Ásgeirsson, G. Georgsson, 1991 .

Hereditary cystatin C (γ‐trace) amyloid angiopathy of the CNS causing cerebral hemorrhage

B. Frangione, Ó. Jensson, A. Grubb, 1987 .

MUTATION IN THE CYSTATIN C GENE CAUSES HEREDITARY CYSTATINC AMYLOID ANGIOPATHY WITH CEREBRAL HEMORRHAGE

I. Olafsson, M. Abrahamson, Ó. Jensson, 1988 .

Distribution of Cystatin C Amyloid Deposits in the Icelandic Patients with Hereditary Cystatin C Amyloid Angiopathy

G. Gudmundsson, Ó. Jensson, L. Thorsteinsson, 1988 .

Molecular Biology of Hereditary Cystatin C Amyloid Angiopathy in Iceland

M. Abrahamson, Ó. Jensson, A. Grubb, 1991 .

GLO polymorphism in Iceland.

Ó. Jensson, A. Árnason, S. Karlsson, 1980, Human Heredity.

Hereditary Elliptocytosis in Iceland

Ó. Jensson, O. Olafsson, T. Jonasson, 1967, British journal of haematology.

The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms.

I. Olafsson, Ó. Jensson, Anders Grubb, 1990, Scandinavian journal of clinical and laboratory investigation.

Serum esterases of Icelanders 1. A “silent” pseudocholinesterase gene in an icelandic family

Ó. Jensson, A. Árnason, Olafur Jensson, 1975, Clinical genetics.