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Sigvard Olsson

Showing results (11-20 of 18) with videos related to

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European Journal of Haematology|March 28, 2008
HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central SwedenK Sigvard Olsson, Bernd Ritter, Norbeth Hansson, et al.
World Journal of Hepatology|September 26, 2022
Hemorrhagic colitis induced by trientine in a 51-year-old patient with Wilson's disease waiting for liver transplantation: A case reportAndreas Schult, Matts Andersson, Jorge Asin-Cayuela, et al.
European Journal of Haematology|October 16, 2010
Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of SwedenKarl Sigvard Olsson, Jan Konar, Inge Hoegh Dufva, et al.
The Journal of Nutritional Biochemistry|May 23, 2008
Hepcidin, interleukin-6 and hematological iron markers in males before and after heart surgeryMichael Hoppe, Bo Lönnerdal, Bakhtiar Hossain, et al.
Hereditas|December 23, 2017
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the <i>WHRN</i> and <i>TMC1</i> genesK Sigvard Olsson, Olof Wålinder, Ulf Jansson, et al.
Scandinavian Journal of Gastroenterology|June 17, 2011
Health check-ups and family screening allow detection of hereditary hemochromatosis with less advanced liver fibrosis and survival comparable with the general populationSoo Aleman, Sanam Endalib, Per Stål, et al.
Gastroenterology|July 23, 2009
Increased mortality risk in patients with phenotypic hereditary hemochromatosis but not in their first-degree relativesMaria Elmberg, Rolf Hultcrantz, Fereshte Ebrahim, et al.
Gastroenterology|January 16, 2004
Cancer risk in patients with hereditary hemochromatosis and in their first-degree relativesMaria Elmberg, Rolf Hultcrantz, Anders Ekbom, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
European Journal of Haematology|March 28, 2008
HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central SwedenK Sigvard Olsson, Bernd Ritter, Norbeth Hansson, et al.
World Journal of Hepatology|September 26, 2022
Hemorrhagic colitis induced by trientine in a 51-year-old patient with Wilson's disease waiting for liver transplantation: A case reportAndreas Schult, Matts Andersson, Jorge Asin-Cayuela, et al.
European Journal of Haematology|October 16, 2010
Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of SwedenKarl Sigvard Olsson, Jan Konar, Inge Hoegh Dufva, et al.
The Journal of Nutritional Biochemistry|May 23, 2008
Hepcidin, interleukin-6 and hematological iron markers in males before and after heart surgeryMichael Hoppe, Bo Lönnerdal, Bakhtiar Hossain, et al.
Hereditas|December 23, 2017
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the <i>WHRN</i> and <i>TMC1</i> genesK Sigvard Olsson, Olof Wålinder, Ulf Jansson, et al.
Scandinavian Journal of Gastroenterology|June 17, 2011
Health check-ups and family screening allow detection of hereditary hemochromatosis with less advanced liver fibrosis and survival comparable with the general populationSoo Aleman, Sanam Endalib, Per Stål, et al.
Gastroenterology|July 23, 2009
Increased mortality risk in patients with phenotypic hereditary hemochromatosis but not in their first-degree relativesMaria Elmberg, Rolf Hultcrantz, Fereshte Ebrahim, et al.
Gastroenterology|January 16, 2004
Cancer risk in patients with hereditary hemochromatosis and in their first-degree relativesMaria Elmberg, Rolf Hultcrantz, Anders Ekbom, et al.
Pageof 2