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Hermann Heimpel

Showing results (11-20 of 36) with videos related to

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Haematologica|November 21, 2007
A new type of transfusion-dependent congenital dyserythropoietic anemiaHermann Heimpel, Elisabeth Kohne, Lothar Schrod, et al.
Haematologica|April 28, 2010
The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cellsHermann Heimpel, Kerstin Kellermann, Nadine Neuschwander, et al.
Annals of Hematology|June 13, 2006
Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapyJeroen S Goede, Rudolf Benz, Joerg Fehr, et al.
Cytometry. Part B, Clinical Cytometry|September 3, 2014
Towards the harmonization of result presentation for the eosin-5'- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosisLinda Hunt, David Greenwood, Hermann Heimpel, et al.
Cytometry. Part B, Clinical Cytometry|September 18, 2014
Toward the harmonization of result presentation for the eosin-5'-maleimide binding test in the diagnosis of hereditary spherocytosisLinda Hunt, David Greenwood, Hermann Heimpel, et al.
Journal of Psychosomatic Research|October 29, 2005
Coping and survival in patients with leukemia undergoing allogeneic bone marrow transplantation--long-term follow-up of a prospective studyNorbert Grulke, Harald Bailer, Bernd Hertenstein, et al.
Blood|November 2, 2002
Tumor necrosis factor receptor-associated factor 1 gene overexpression in B-cell chronic lymphocytic leukemia: analysis of NF-kappa B/Rel-regulated inhibitors of apoptosisGerd Munzert, Dieter Kirchner, Heike Stobbe, et al.
Glycoconjugate Journal|January 2, 2008
Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS)Jonas Denecke, Christian Kranz, Manfred Nimtz, et al.
Annals of Hematology|June 26, 2008
Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-geneYong Xi Ru, Xiao-fan Zhu, Wen-wei Yan, et al.
Annals of Hematology|October 6, 2010
Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 (G208R) mutationUlrich Dührsen, Christian P Kratz, Christian Flotho, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Haematologica|November 21, 2007
A new type of transfusion-dependent congenital dyserythropoietic anemiaHermann Heimpel, Elisabeth Kohne, Lothar Schrod, et al.
Haematologica|April 28, 2010
The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cellsHermann Heimpel, Kerstin Kellermann, Nadine Neuschwander, et al.
Annals of Hematology|June 13, 2006
Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapyJeroen S Goede, Rudolf Benz, Joerg Fehr, et al.
Cytometry. Part B, Clinical Cytometry|September 3, 2014
Towards the harmonization of result presentation for the eosin-5'- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosisLinda Hunt, David Greenwood, Hermann Heimpel, et al.
Cytometry. Part B, Clinical Cytometry|September 18, 2014
Toward the harmonization of result presentation for the eosin-5'-maleimide binding test in the diagnosis of hereditary spherocytosisLinda Hunt, David Greenwood, Hermann Heimpel, et al.
Journal of Psychosomatic Research|October 29, 2005
Coping and survival in patients with leukemia undergoing allogeneic bone marrow transplantation--long-term follow-up of a prospective studyNorbert Grulke, Harald Bailer, Bernd Hertenstein, et al.
Blood|November 2, 2002
Tumor necrosis factor receptor-associated factor 1 gene overexpression in B-cell chronic lymphocytic leukemia: analysis of NF-kappa B/Rel-regulated inhibitors of apoptosisGerd Munzert, Dieter Kirchner, Heike Stobbe, et al.
Glycoconjugate Journal|January 2, 2008
Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS)Jonas Denecke, Christian Kranz, Manfred Nimtz, et al.
Annals of Hematology|June 26, 2008
Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-geneYong Xi Ru, Xiao-fan Zhu, Wen-wei Yan, et al.
Annals of Hematology|October 6, 2010
Long-term outcome of hemizygous and heterozygous carriers of a germline GATA1 (G208R) mutationUlrich Dührsen, Christian P Kratz, Christian Flotho, et al.
Pageof 4