Pathological changes in basement membranes and dermal connective tissue of skin from patients with hereditary cystatin C amyloid angiopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology,Pathology and Forensic Medicine
Link
http://www.nature.com/articles/labinvest2016133.pdf
Reference50 articles.
1. Jensson O, Gudmundsson G, Arnason A et al, Hereditary cystatin C (gamma-trace) amyloid angiopathy of the CNS causing cerebral hemorrhage. Acta Neurol Scand 1987; 76: 102–114.
2. Gudmundsson G, Hallgrimsson J, Jonasson TA et al, Hereditary cerebral haemorrhage with amyloidosis. Brain 1972; 95: 387–404.
3. Cohen DH, Feiner H, Jensson O et al, Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace. J Exp Med 1983; 158: 623–628.
4. Ghiso J, Jensson O, Frangione B . Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C). Proc Natl Acad Sci USA 1986; 83: 2974–2978.
5. Levy E, Lopez-Otin C, Ghiso J et al, Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases. J Exp Med 1989; 169: 1771–1778.
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