Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Elma Scheibel"'
Publikováno v:
Scandinavian Journal of Haematology. 32:544-551
Screening of 43 healthy Danish haemophiliacs revealed a significantly lower helper/suppressor (H/S) ratio than in controls. 8 of the haemophiliacs had an H/S ratio less than or equal to 1.0. A significant negative correlation occurred between the tot
Autor:
J. Dalsgård Nielsen, J. Gerstoft, B. Ørskov Lindhardt, Ebbe Dickmeiss, Elma Scheibel, K. Bentzen, K. Ulrich
Publikováno v:
Scandinavian Journal of Haematology. 35:379-385
18 out of 40 healthy Danish type A haemophiliacs had antibodies against HTLV-III as measured by an enzyme linked immunosorbent assay (ELISA). The overall seropositivity was 45%. A significant positive correlation was found between seropositivity and
Publikováno v:
European Journal of Haematology. 61:11-14
Significant advances have been achieved in prevention of haemophilic disability through prophylactic administration of concentrates and early administration of coagulation factors to control new bleeding episodes, but there is only limited experience
Autor:
Jørn Attermann, Arne Svejgaard, Peter Skinhøj, Claus Bohn Christiansen, Sam Schulman, Jørgen Ingerslev, Astrid K. N. Iversen, Erik Berntorp, Jan Gerstoft, Ebbe Dickmeiss, Elma Scheibel, L Tengborn, Lars Fugger, Jesper Eugen-Olsen
Publikováno v:
Iversen, A K N, Christiansen, C B, Attermann, J, Eugen-Olsen, J, Schulman, S, Berntop, E, Ingerslev, J, Fugger, L H, Scheibel, E, Tengborn, L, Gerstoft, J, Dickmeiss, E, Svejgaard, A & Skinhøj, P 2003, ' Limited protective effect of the CCR5Δ32/CCR5Δ32 genotype on human immunodeficiency virus infection incidence in a cohort of patients with hemophilia and selection for genotypic X4 virus ', Journal of Infectious Diseases, vol. 187, no. 2, pp. 215-225 . https://doi.org/10.1086/345881
Iversen, A K N, Christiansen, C B, Attermann, J, Eugen-Olsen, J, Schulman, S, Berntorp, E, Ingerslev, J, Fugger, L, Scheibel, E, Tengborn, L, Gerstoft, J, Dickmeiss, E, Svejgaard, A & Skinhøj, P 2003, ' Limited protective effect of the CCR5Delta32/CCR5Delta32 genotype on human immunodeficiency virus infection incidence in a cohort of patients with hemophilia and selection for genotypic X4 virus. ', Journal of Infectious Diseases, vol. 187, no. 2, pp. 215-25 .
Iversen, J, Christiansen, C B, Attermann, J, Eugen-Olsen, J, Schulman, S, Berntorp, E, Ingerslev, J, Fugger, L, Scheibel, E, Tengborn, L, Gerstoft, J, Dickmeiss, E, Svejgaard, A & Skinhoj, P 2003, ' Limited protective effect of the CCR5Delta32/CCR5Delta32 genotype on human immunodificiency virus infection incidence in a cohort of patients with hemophilia and selection for genotypic X4 virus ', J Infect Dis, vol. 2, no. 187, pp. 215-225 .
Iversen, A K N, Christiansen, C B, Attermann, J, Eugen-Olsen, J, Schulman, S, Berntorp, E, Ingerslev, J, Fugger, L, Scheibel, E, Tengborn, L, Gerstoft, J, Dickmeiss, E, Svejgaard, A & Skinhøj, P 2003, ' Limited protective effect of the CCR5Delta32/CCR5Delta32 genotype on human immunodeficiency virus infection incidence in a cohort of patients with hemophilia and selection for genotypic X4 virus. ', Journal of Infectious Diseases, vol. 187, no. 2, pp. 215-25 .
Iversen, J, Christiansen, C B, Attermann, J, Eugen-Olsen, J, Schulman, S, Berntorp, E, Ingerslev, J, Fugger, L, Scheibel, E, Tengborn, L, Gerstoft, J, Dickmeiss, E, Svejgaard, A & Skinhoj, P 2003, ' Limited protective effect of the CCR5Delta32/CCR5Delta32 genotype on human immunodificiency virus infection incidence in a cohort of patients with hemophilia and selection for genotypic X4 virus ', J Infect Dis, vol. 2, no. 187, pp. 215-225 .
Udgivelsesdato: 2003-Jan-15 The relationship among CCR5 genotype, cytomegalovirus infection, and disease progression and death was studied among 159 human immunodeficiency virus (HIV)-infected patients with hemophilia. One patient (0.6%) had the CCR5
Autor:
Anne, Jung, Katharina Maria, Main, Elma, Scheibel, Birgit, Peitersen, Niels, Clausen, Gunna, Erichsen, Kjeld, Schmiegelow, Niels, Illum
Publikováno v:
Ugeskrift for laeger. 164(49)
Beta-thalassemia major occurs with increasing frequency among Danish children as a result of immigration. The aim of the study was to estimate the occurrence of beta-thalassemia major in Denmark, analyse the treatment and organ functions, and identif
Autor:
Anne Jung, Katharina Maria Main, Elma Scheibel, Birgit Peitersen, Niels Clausen, Gunna Erichsen, Kjeld Schmiegelow, Niels Ove Illum
Publikováno v:
Jung, A, Main, K M, Scheibel, E, Peitersen, B, Clausen, N, Erichsen, G, Schmiegelow, K & Illum, N 2002, ' beta-thalassaemia major hos børn og unge i Danmark ', Ugeskrift for Laeger, bind 164, nr. 49, s. 5803-6 .
Capital Region of Denmark
Jung, A, Main, K M, Scheibel, E, Peitersen, B, Clausen, N, Erichsen, G, Schmiegelow, K & Illum, N 2002, ' Beta-thalassaemia major hos børn og unge i Danmark ' Ugeskr. Læg., bind 164, s. 5803-5806 .
University of Southern Denmark
Capital Region of Denmark
Jung, A, Main, K M, Scheibel, E, Peitersen, B, Clausen, N, Erichsen, G, Schmiegelow, K & Illum, N 2002, ' Beta-thalassaemia major hos børn og unge i Danmark ' Ugeskr. Læg., bind 164, s. 5803-5806 .
University of Southern Denmark
INTRODUCTION: Beta-thalassemia major occurs with increasing frequency among Danish children as a result of immigration. The aim of the study was to estimate the occurrence of beta-thalassemia major in Denmark, analyse the treatment and organ function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4bcf7f43c9314d57870be760c5a536f9
https://portal.findresearcher.sdu.dk/da/publications/c8bea560-3dd6-49b5-9c8c-bac3b6f2c012
https://portal.findresearcher.sdu.dk/da/publications/c8bea560-3dd6-49b5-9c8c-bac3b6f2c012
Publikováno v:
Thrombosis and haemostasis. 83(3)
SummaryHaemophilia A and B are X-linked disorders which are due to a reduced activity of coagulation factor VIII or IX, respectively. Female carriers have a wide range of plasma concentration of factor VIII or factor IX, and may in rare cases have an
Publikováno v:
Clinical Genetics. 29:472-473
Publikováno v:
Thrombosis and haemostasis. 73(5)
SummaryHemophilia B is caused by a wide range of mutations. In order to characterize the mutations among patients in Denmark, we have systematically screened the entire coding region, the promoter region and exon flanking sequences of the gene encodi
Autor:
Bjöurn Dahlbäck, Lars Holmberg, Harald Lenk, Mikael Donnér, Inga Marie Nilsson, Elma Scheibel, Ann-Charlotte Kristoffersson
Publikováno v:
British journal of haematology. 82(1)
Type IIB of von Willebrand's disease (vWD) is a variant in which the structurally abnormal von Willebrand factor (vWF) shows an increased affinity for the platelet vWF receptor, glycoprotein Ib (GPIb). This may sometimes give rise to platelet aggrega