Immune reactions associated with cerebral amyloid angiopathy von YAMADA, M, ITOH, Y, SHINTAKU, M, KAWAMURA, J, JENSSON, O, THORSTEINSSON, L, SUEMATSU, N, MATSUSHITA, M, OTOMO, E

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Structure and expression of the human cystatin C gene von Abrahamson, M, Olafsson, I, Palsdottir, A, Ulvsbäck, M, Lundwall, A, Jensson, O, Grubb, A

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The Molecular Pathology of Hereditary Cystatin C Amyloid Angiopathy Causing Brain Hemorrhage von Ólafsson, Ísleifur, Thorsteinsson, Leifur, Jensson, Ólafur

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Amyloid Fibrils in Hereditary Cerebral Hemorrhage with Amyloidosis of Icelandic Type is a Variant of γ -trace Basic Protein (Cystatin C) von Ghiso, Jorge, Jensson, Olafur, Frangione, Blas

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The application of molecular genetics to detection of craniofacial abnormality von Moore, G, Ivens, A, Chambers, J, Bjornsson, A, Arnason, A, Jensson, O, Williamson, R

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HEREDITARY CYSTATIN-C AMYLOID ANGIOPATHY - IDENTIFICATION OF THE DISEASE-CAUSING MUTATION AND SPECIFIC DIAGNOSIS BY POLYMERASE CHAIN-REACTION BASED ANALYSIS von ABRAHAMSON, M, JONSDOTTIR, S, OLAFSSON, JENSSON, O, GRUBB, A

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Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2 von Sykes, B, Ogilvie, D, Wordsworth, P, Wallis, G, Mathew, C, Beighton, P, Nicholls, A, Pope, F M, Thompson, E, Tsipouras, P

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Microvascular degeneration in hereditary cystatin C amyloid angiopathy of the brain von WANG, ZHEN ZHEN, JENSSON, OLAFUR, THORSTEINSSON, LEIFUR, VINTERS, HARRY V.

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Abnormal Metabolism of γ-Trace Alkaline Microprotein: The Basic Defect in Hereditary Cerebral Hemorrhage with Amyloidosis von Grubb, Anders, Jensson, Olafur, Gudmundsson, Gunnar, Arnason, Alfred, Löfberg, Helge, Malm, Johan

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Amyloid fibril in hereditary cerebral hemorrhage with amyloidosis (HCHWA) is related to the gastroentero-pancreatic neuroendocrine protein, gamma trace von Cohen, D H, Feiner, H, Jensson, O, Frangione, B

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Gc Subtypes in Icelanders von Karlsson, Stefan, Skaftadóttir, Inga, Árnason, Alfred, Thórdarson, Gudmundur, Jensson, Ólafur

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Human cystatin C expression and regulation by TGF-β1: Implications for the pathogenesis of hereditary cystatin C amyloid angiopathy causing brain hemorrhage von Emilsson, Valur, Thorsteinsson, Leifur, Jensson, Olafur, Gudnnundsson, Gunnar

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Linkage of an X-chromosome cleft palate gene von Moore, Gudrun E, Ivens, Alasdair, Chambers, Joanna, Farrall, Martin, Williamson, Robert, Page, David C, Bjornsson, Ami, Arnason, Alfred, Jensson, Olafur

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Immunohistochemical characterization of the amyloid deposits and quantitation of pertinent cerebrospinal fluid proteins in hereditary cerebral hemorrhage with amyloidosis von Löfberg, H, Grubb, A O, Nilsson, E K, Jensson, O, Gudmundsson, G, Blöndal, H, Arnason, A, Thorsteinsson, L

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Missense mutations causing mild hemophilia A in Iceland detected by denaturing gradient gel electrophoresis von Jonsdottir, Sif, Diamond, Carol, Levinson, Barbara, Magnusson, Sigmundur, Jensson, Olafur, Gitschier, Jane

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Wilson disease in Iceland : a clinical and genetic study von THOMAS, G. R, JENSSON, O, GUDMUNDSSON, G, THORSTEINSSON, L, COX, D. W

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Abnormal Metabolism of [gamma]-Trace Alkaline Microprotein: The Basic Defect in Hereditary Cerebral Hemorrhage with Amyloidosis von Grubb, Anders, Jensson, Olafur, Gudmundsson, Gunnar, Arnason, Alfred, Löfberg, Helge, Malm, Johan

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Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15 von Fossdal, Ragnheidur, Magnússon, Loftur, Weber, James L., Jensson, Ólafur

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On the role of monocytes/macrophages in the pathogenesis of central nervous system lesions in hereditary cystatin C amyloid angiopathy von Thorsteinsson, Leifur, Georgsson, Gudmundur, Ásgeirsson, Bjarni, Bjarnadóttir, María, Ólafsson, Ísleifur, Jensson, Ólafur, Gudmundsson, Gunnar

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Icelandic families with autosomal dominant polycystic kidney disease : families unlinked to chromosome 16p13.3 revealed by linkage analysis von FOSSDAL, R, BÖOVARSSON, M, ASMUNDSSON, P, RAGNARSSON, J, PETERS, D, BREUNING, M. H, JENSSON, O

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