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Sigvard Olsson

Showing results (1-10 of 18) with videos related to

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Lakartidningen|December 4, 2003
[Background of iron deficiency as a symptom should be assessed]Sigvard Olsson
Lakartidningen|February 11, 2015
[Born in the foyer of the Grand Hotel in Lund]Sigvard Olsson
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|September 17, 2009
[Hemochromatosis]K Sigvard Olsson
Lakartidningen|February 25, 2016
[Was the boat packed with hemochromatosis?]K Sigvard Olsson
EJIFCC|November 16, 2018
Hereditary Hemochromatosis and Iron MetabolismJoyce Carlson, Sigvard Olsson
European Journal of Haematology|September 22, 2011
Letter to the editorSigvard Olsson, Ruma Raha-Chowdhury
Haematologica|June 3, 2008
Comment to: Hepcidin: from discovery to differential diagnosis. Haematologica 2008; 93:90-7K Sigvard Olsson, Anders Norrby
European Journal of Haematology|October 11, 2007
The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?K Sigvard Olsson, Bernd Ritter, Norbeth Hansson
European Journal of Haematology|November 17, 2009
HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overloadK Sigvard Olsson, Bernd Ritter, Ruma Raha-Chowdhury
Scandinavian Journal of Gastroenterology|July 11, 2012
Common local founder effects for Wilson's disease and hereditary hemochromatosis; mutation studies of a large familyKarl Sigvard Olsson, Olof Wålinder, Andreas Kindmark, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Lakartidningen|December 4, 2003
[Background of iron deficiency as a symptom should be assessed]Sigvard Olsson
Lakartidningen|February 11, 2015
[Born in the foyer of the Grand Hotel in Lund]Sigvard Olsson
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|September 17, 2009
[Hemochromatosis]K Sigvard Olsson
Lakartidningen|February 25, 2016
[Was the boat packed with hemochromatosis?]K Sigvard Olsson
EJIFCC|November 16, 2018
Hereditary Hemochromatosis and Iron MetabolismJoyce Carlson, Sigvard Olsson
European Journal of Haematology|September 22, 2011
Letter to the editorSigvard Olsson, Ruma Raha-Chowdhury
Haematologica|June 3, 2008
Comment to: Hepcidin: from discovery to differential diagnosis. Haematologica 2008; 93:90-7K Sigvard Olsson, Anders Norrby
European Journal of Haematology|October 11, 2007
The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?K Sigvard Olsson, Bernd Ritter, Norbeth Hansson
European Journal of Haematology|November 17, 2009
HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overloadK Sigvard Olsson, Bernd Ritter, Ruma Raha-Chowdhury
Scandinavian Journal of Gastroenterology|July 11, 2012
Common local founder effects for Wilson's disease and hereditary hemochromatosis; mutation studies of a large familyKarl Sigvard Olsson, Olof Wålinder, Andreas Kindmark, et al.
Pageof 2