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Items: 1 to 50 of 68

1.

Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the brain.

Wang ZZ, Jensson O, Thorsteinsson L, Vinters HV.

APMIS. 1997 Jan;105(1):41-7.

PMID:
9063500
2.

Immune reactions associated with cerebral amyloid angiopathy.

Yamada M, Itoh Y, Shintaku M, Kawamura J, Jensson O, Thorsteinsson L, Suematsu N, Matsushita M, Otomo E.

Stroke. 1996 Jul;27(7):1155-62.

PMID:
8685920
3.

The molecular pathology of hereditary cystatin C amyloid angiopathy causing brain hemorrhage.

Olafsson I, Thorsteinsson L, Jensson O.

Brain Pathol. 1996 Apr;6(2):121-6. Review.

PMID:
8737928
4.

[Mild haemophilia A in Iceland.].

Jensson O, Jonsdottir S.

Laeknabladid. 1995 Jun;81(6):477-83. Icelandic.

PMID:
20065483
5.

Wilson disease in Iceland: a clinical and genetic study.

Thomas GR, Jensson O, Gudmundsson G, Thorsteinsson L, Cox DW.

Am J Hum Genet. 1995 May;56(5):1140-6.

6.
7.

Familial macroglobulinaemia: hyperactive B-cells but normal natural killer function.

Ogmundsdóttir HM, Jóhannesson GM, Sveinsdóttir S, Einarsdóttir S, Hegeman A, Jensson O, Ogsmundsdóttir HM.

Scand J Immunol. 1994 Aug;40(2):195-200. Erratum in: Scand J Immunol 1995 Jun;41(6):650.

PMID:
8047841
8.

Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation.

Jensson O, Stenbjerg Bernvil S, Jónsdóttir S, Ingerslev J.

J Intern Med. 1994 May;235(5):443-50.

PMID:
8182400
9.

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

Haan J, Maat-Schieman ML, van Duinen SG, Jensson O, Thorsteinsson L, Roos RA.

Acta Neurol Scand. 1994 May;89(5):367-71.

PMID:
8085435
10.

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.

Newton R, Stanier P, Loughna S, Henderson DJ, Forbes SA, Farrall M, Jensson O, Moore GE.

Clin Genet. 1994 May;45(5):241-9.

PMID:
8076409
11.

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

Hol FA, Geurds MP, Jensson O, Hamel BC, Moore GE, Newton R, Mariman EC.

Hum Genet. 1994 Apr;93(4):452-6.

PMID:
8168816
12.

[Transfusion medicine--Scandinavian recommendations].

Jørgensen J, Jensson O, Eklund J, Kornstad L, Messeter L.

Nord Med. 1994;109(2):61-3. Danish.

PMID:
8121792
13.

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

Fossdal R, Böthvarsson M, Asmundsson P, Ragnarsson J, Peters D, Breuning MH, Jensson O.

Hum Genet. 1993 Jul;91(6):609-13.

PMID:
8340115
14.
15.

On the role of monocytes/macrophages in the pathogenesis of central nervous system lesions in hereditary cystatin C amyloid angiopathy.

Thorsteinsson L, Georgsson G, Asgeirsson B, Bjarnadóttir M, Olafsson I, Jensson O, Gudmundsson G.

J Neurol Sci. 1992 Apr;108(2):121-8.

PMID:
1517744
16.

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

Ogmundsdóttir HM, Thorsteinsson L, Sigfússon A, Sveinsdóttir S, Björnsson S, Eyjólfsson G, Jóhannesson GM, Jensson O.

APMIS. 1992 Jan;100(1):10-20.

PMID:
1536717
17.

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

Jonsdottir S, Diamond C, Levinson B, Magnusson S, Jensson O, Gitschier J.

Hum Mutat. 1992;1(6):506-8. No abstract available.

PMID:
1301960
18.

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

Moore GE, Williamson R, Jensson O, Chambers J, Takakubo F, Newton R, Balacs MA, Ivens A.

J Craniofac Genet Dev Biol. 1991 Oct-Dec;11(4):372-6.

PMID:
1687471
19.

[Scandinavian recommendations for transfusion medicine].

Eklund J, Jørgensen J, Högman C, Jensson O, Kornstad L.

Nord Med. 1991;106(11):299-300. Swedish.

PMID:
1945807
20.

Three RFLPs at the 3' end of the cystatin C gene, the disease gene in hereditary cystatin C amyloid angiopathy (HCCAA) in Iceland.

Palsdottir A, Jonsdottir S, Abrahamson M, Grubb A, Jensson O.

Nucleic Acids Res. 1990 Dec 25;18(24):7471. No abstract available.

21.

The first Icelandic family with X-linked agammaglobulinaemia: studies of genetic markers and immune function.

Thorsteinsson L, Ogmundsdóttir HM, Sigfússon A, Arnason A, Eyjólfsson G, Jensson O.

Scand J Immunol. 1990 Sep;32(3):273-80.

PMID:
2402596
22.

Structure and expression of the human cystatin C gene.

Abrahamson M, Olafsson I, Palsdottir A, Ulvsbäck M, Lundwall A, Jensson O, Grubb A.

Biochem J. 1990 Jun 1;268(2):287-94.

23.

Cystatin C mutation causing amyloid angiopathy and brain hemorrhage.

Jensson O, Pálsdóttir A, Thorsteinsson L, Arnason A, Abrahamson M, Olafsson I, Grubb A.

Biol Chem Hoppe Seyler. 1990 May;371 Suppl:229-32. No abstract available.

PMID:
2169252
24.

X chromosome genes involved in the regulation of facial clefting and spina bifida.

Moore GE, Ivens A, Newton R, Balacs MA, Henderson DJ, Jensson O.

Cleft Palate J. 1990 Apr;27(2):131-5. Review.

PMID:
2187632
25.
26.

[Recommendations from the 12th Scandinavian meeting on transfusion medicine].

Eklund J, Jørgensen J, Högman C, Jensson O, Kornstad L.

Nord Med. 1990;105(4):119-20. Danish. No abstract available.

PMID:
2111542
27.

The saga of cystatin C gene mutation causing amyloid angiopathy and brain hemorrhage--clinical genetics in Iceland.

Jensson O, Palsdottir A, Thorsteinsson L, Arnason A.

Clin Genet. 1989 Nov;36(5):368-77. Review.

PMID:
2689007
28.

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

Yamada M, Tsukagoshi H, Wada Y, Otomo E, Hayakawa M, Thorsteinsson L, Jensson O.

Acta Neurol Scand. 1989 Jun;79(6):504-9.

PMID:
2782031
29.

[Norwegian propositions for blood transfusion practices].

Högman C, Jensson O, Eklund J, Kornstad L, Jörgensen J.

Nord Med. 1989;104(3):83-4. Swedish. No abstract available.

PMID:
2922255
30.

Mutation in the cystatin C gene causes hereditary brain hemorrhage.

Palsdottir A, Abrahamson M, Thorsteinsson L, Arnason A, Olafsson I, Grubb A, Jensson O.

Prog Clin Biol Res. 1989;317:241-6.

PMID:
2602420
31.

Mutation in cystatin C gene causes hereditary brain haemorrhage.

Palsdottir A, Abrahamson M, Thorsteinsson L, Arnason A, Olafsson I, Grubb A, Jensson O.

Lancet. 1988 Sep 10;2(8611):603-4.

PMID:
2900981
32.

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

Jensson O, Arnason A, Gunnarsdottir H, Petursdottir I, Fossdal R, Hreidarsson S.

J Med Genet. 1988 Apr;25(4):227-9.

33.

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

Ivens A, Moore GE, Chambers J, Arnason A, Jensson O, Bjornsson A, Williamson R.

Hum Genet. 1988 Apr;78(4):356-8.

PMID:
2896158
34.

The application of molecular genetics to detection of craniofacial abnormality.

Moore G, Ivens A, Chambers J, Bjornsson A, Arnason A, Jensson O, Williamson R.

Development. 1988;103 Suppl:233-9.

PMID:
3074911
35.

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

Jensson O, Gudmundsson G, Arnason A, Blöndal H, Petursdottir I, Thorsteinsson L, Grubb A, Löfberg H, Cohen D, Frangione B.

Acta Neurol Scand. 1987 Aug;76(2):102-14.

PMID:
3673496
36.

Gene organization of haplotypes expressing two different C4A allotypes.

Palsdottir A, Arnason A, Fossdal R, Jensson O.

Hum Genet. 1987 Jul;76(3):220-4.

PMID:
3036685
37.

Bgl II polymorphic site upstream to the human complement component C4A gene.

Palsdottir A, Fossdal R, Jensson O, Arnason A.

Nucleic Acids Res. 1987 Mar 11;15(5):2395. No abstract available.

38.

Linkage of an X-chromosome cleft palate gene.

Moore GE, Ivens A, Chambers J, Farrall M, Williamson R, Page DC, Bjornsson A, Arnason A, Jensson O.

Nature. 1987 Mar 5-11;326(6108):91-2.

PMID:
2881212
39.

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

Löfberg H, Grubb AO, Nilsson EK, Jensson O, Gudmundsson G, Blöndal H, Arnason A, Thorsteinsson L.

Stroke. 1987 Mar-Apr;18(2):431-40.

PMID:
2436360
40.

Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes.

Palsdottir A, Fossdal R, Arnason A, Edwards JH, Jensson O.

Immunogenetics. 1987;25(5):299-304.

PMID:
2883116
41.
42.

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

Grubb A, Jensson O, Gudmundsson G, Arnason A, Löfberg H, Malm J.

N Engl J Med. 1984 Dec 13;311(24):1547-9. No abstract available.

PMID:
6390199
43.

Immunohistochemical demonstration of amyloid P component in cerebro-vascular amyloidosis.

Rowe IF, Jensson O, Lewis PD, Candy J, Tennent GA, Pepys MB.

Neuropathol Appl Neurobiol. 1984 Jan-Feb;10(1):53-61.

PMID:
6377111
45.

An unusual Rhesus haplotype, --D--, in Iceland.

Olafsdóttir S, Jensson O, Thordarson G, Sigurdardóttir S.

Forensic Sci Int. 1983 Aug-Sep;22(2-3):183-7.

PMID:
6416954
46.

Gc subtypes in Icelanders.

Karlsson S, Skaftadóttir I, Arnason A, Thórdarson G, Jensson O.

Hum Hered. 1983;33(1):5-8.

PMID:
6840779
47.

Gc subtypes in Northern Indians.

Karlsson S, Skaftadóttir I, Arnason A, Mackintosh P, Jensson O.

Hum Hered. 1983;33(3):199-200.

PMID:
6688237
48.

Epidemiology of delta infection in Scandinavia.

Hansson BG, Norkrans G, Weibull M, Weiland O, Nielsen J, Leinikki P, Ukkonen P, Jensson O, Siebke JC.

Prog Clin Biol Res. 1983;143:155-9. No abstract available.

PMID:
6669568
49.

Selective serum IgA deficiency in Icelanders. Frequency, family studies and Ig levels.

Ulfarsson J, Gudmundsson S, Birgisdóttir B, Kjeld JM, Jensson O.

Acta Med Scand. 1982;211(6):481-7.

PMID:
7113764
50.

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

Jensson O, Björnsson OG, Arnason A, Birgisdóttir B, Pepys MB.

Acta Med Scand. 1982;211(5):341-5.

PMID:
6810656

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