Protein C mutation (A267T) results in ER retention and unfolded protein response activation von Tjeldhorn, Lena, Iversen, Nina, Sandvig, Kirsten, Bergan, Jonas, Sandset, Per Morten, Skretting, Grethe

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Management of Wrong Blood Transfusion to an RhD Negative Woman in Labor von Titze, Thomas Larsen, Hamnvik, Lars Henrik Dahl, Hauglum, Inga Marie, Carlsen, Anne Elisabeth Tonay, Tjeldhorn, Lena, Nguyen, Nhan Trung, Akkök, Çiğdem Akalın

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Abstract CT016: A first in man phase I/II adjuvant dendritic cell vaccine study in high-risk prostate cancer patients following radical surgery reduce the incidence of biochemical... von Tryggestad, Anne Merete, Bigalke, Iris, Axcrona, Karol, Brennhovd, Bjørn, Hønnåshagen, T Kirsti, Skoge, Lisbeth, Tjeldhorn, Lena, Mowinckel, Lene, Sæbøe-Larsen, Stein, Jørgensen, Jens A L, Andreassen, Grete S, Skorstad, Gjertrud, Josefsen, Dag, Axcrona, Ulrika, Aamadal, Steinar, Lilleby, Wolfgang, Dueland, Svein, Kvalheim, Gunnar

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Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis von Tjeldhorn, Lena, Sandset, Per Morten, Haugbro, Kaia, Skretting, Grethe

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Qualitative and quantitative analysis of FBN1 mRNA from 16 patients with Marfan Syndrome von Tjeldhorn, Lena, Amundsen, Silja Svanstrøm, Barøy, Tuva, Rand-Hendriksen, Svend, Geiran, Odd, Frengen, Eirik, Paus, Benedicte

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Protein C Mutation von Tjeldhorn, Lena, Iversen, Nina, Sandvig, Kirsten, Bergan, Jonas, Sandset, Per Morten, Skretting, Grethe

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Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome von RAND-HENDRIKSEN, Svend, LUNDBY, Rigmor, TJELDHORN, Lena, ANDERSEN, Kai, OFFSTAD, Jon, OVE SEMB, Svein, SMITH, Hans-Jørgen, PAUS, Benedicte, GEIRAN, Odd

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Functional characterization of the protein C A267T mutation: evidence for impaired secretion due to defective intracellular transport von Tjeldhorn, Lena, Iversen, Nina, Sandvig, Kirsten, Bergan, Jonas, Sandset, Per Morten, Skretting, Grethe

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Search for correlations between FBN1 genotype and complete Ghent phenotype in 44 unrelated Norwegian patients with Marfan syndrome von Rand-Hendriksen, Svend, Tjeldhorn, Lena, Lundby, Rigmor, Semb, Svein Ove, Offstad, Jon, Andersen, Kai, Geiran, Odd, Paus, Benedicte

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Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome von Rand-hendriksen, Svend, Lundby, Rigmor, Tjeldhorn, Lena, Andersen, Kai, Offstad, Jon, Semb, Svein Ove, Smith, Hans-jørgen, Paus, Benedicte, Geiran, Odd

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Erratum: Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome von Rand-Hendriksen, Svend, Lundby, Rigmor, Tjeldhorn, Lena, Andersen, Kai, Offstad, Jon, Semb, Svein Ove, Smith, Hans-Jørgen, Paus, Benedicte, Geiran, Odd

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Additional file 1: of Qualitative and quantitative analysis of FBN1 mRNA from 16 patients with Marfan Syndrome von Tjeldhorn, Lena, Amundsen, Silja, Tuva BarøY, Rand-Hendriksen, Svend, Geiran, Odd, Frengen, Eirik, Paus, Benedicte

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