158 related articles for article (PubMed ID: 1352269)
1. Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis.
Abrahamson M; Jonsdottir S; Olafsson I; Jensson O; Grubb A
Hum Genet; 1992 Jun; 89(4):377-80. PubMed ID: 1352269
[TBL] [Abstract][Full Text] [Related]
2. Molecular diagnosis of hereditary cystatin C amyloid angiopathy.
Jonsdottir S; Palsdottir A
Biochem Med Metab Biol; 1993 Apr; 49(2):117-23. PubMed ID: 8097919
[TBL] [Abstract][Full Text] [Related]
3. Hereditary cystatin C amyloid angiopathy: monitoring the presence of the Leu-68-->Gln cystatin C variant in cerebrospinal fluids and monocyte cultures by MS.
Asgeirsson B; Haebel S; Thorsteinsson L; Helgason E; Gudmundsson KO; Gudmundsson G; Roepstorff P
Biochem J; 1998 Feb; 329 ( Pt 3)(Pt 3):497-503. PubMed ID: 9445375
[TBL] [Abstract][Full Text] [Related]
4. 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.
Olafsson I; Gudmundsson G; Abrahamson M; Jensson O; Grubb A
Scand J Clin Lab Invest; 1990 Feb; 50(1):85-93. PubMed ID: 2315647
[TBL] [Abstract][Full Text] [Related]
5. 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; 2(8611):603-4. PubMed ID: 2900981
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 8737928
[TBL] [Abstract][Full Text] [Related]
7. The cerebral hemorrhage-producing cystatin C variant (L68Q) in extracellular fluids.
Bjarnadottir M; Nilsson C; Lindström V; Westman A; Davidsson P; Thormodsson F; Blöndal H; Gudmundsson G; Grubb A
Amyloid; 2001 Mar; 8(1):1-10. PubMed ID: 11293820
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 2602420
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 1517744
[TBL] [Abstract][Full Text] [Related]
10. Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2.
Schnittger S; Rao VV; Abrahamson M; Hansmann I
Genomics; 1993 Apr; 16(1):50-5. PubMed ID: 8486384
[TBL] [Abstract][Full Text] [Related]
11. Cystatin C. Icelandic-like mutation in an animal model of cerebrovascular beta-amyloidosis.
Wei LH; Walker LC; Levy E
Stroke; 1996 Nov; 27(11):2080-5. PubMed ID: 8898820
[TBL] [Abstract][Full Text] [Related]
12. Molecular basis for amyloidosis related to hereditary brain hemorrhage.
Abrahamson M
Scand J Clin Lab Invest Suppl; 1996; 226():47-56. PubMed ID: 8981667
[TBL] [Abstract][Full Text] [Related]
13. Hereditary cystatin C amyloid angiopathy: genetic, clinical, and pathological aspects.
Palsdottir A; Snorradottir AO; Thorsteinsson L
Brain Pathol; 2006 Jan; 16(1):55-9. PubMed ID: 16612982
[TBL] [Abstract][Full Text] [Related]
14. An Ala/Thr variation in the coding region of the human cystatin C gene (CST3) detected as a SstII polymorphism.
Balbín M; Grubb A; Abrahamson M
Hum Genet; 1993 Sep; 92(2):206-7. PubMed ID: 8103758
[TBL] [Abstract][Full Text] [Related]
15. Hereditary cystatin C amyloid angiopathy.
Olafsson I; Grubb A
Amyloid; 2000 Mar; 7(1):70-9. PubMed ID: 10842708
[No Abstract] [Full Text] [Related]
16. 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; 18(24):7471. PubMed ID: 1979681
[No Abstract] [Full Text] [Related]
17. 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. PubMed ID: 2689007
[TBL] [Abstract][Full Text] [Related]
18. Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases.
Levy E; Lopez-Otin C; Ghiso J; Geltner D; Frangione B
J Exp Med; 1989 May; 169(5):1771-8. PubMed ID: 2541223
[TBL] [Abstract][Full Text] [Related]
19. Two stable unfolding intermediates of the disease-causing L68Q variant of human cystatin C.
Gerhartz B; Ekiel I; Abrahamson M
Biochemistry; 1998 Dec; 37(49):17309-17. PubMed ID: 9860845
[TBL] [Abstract][Full Text] [Related]
20. No mutations in cystatin C gene in cerebral amyloid angiopathy with cystatin C deposition.
Nagai A; Kobayashi S; Shimode K; Imaoka K; Umegae N; Fujihara S; Nakamura M
Mol Chem Neuropathol; 1998 Jan; 33(1):63-78. PubMed ID: 9493177
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]