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S W Eber

Showing results (31-40 of 47) with videos related to

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American Journal of Human Genetics|May 1, 1980
Characterization of a phosphoglycerate kinase deficiency variants not associated with hemolytic anemiaW K Krietsch, S W Eber, B Haas, et al.
European Journal of Pediatrics|December 14, 1999
Therapy-resistant haemarthros in a patient with factor VIII inhibitor: successful treatment with recombinant factor VIIaE Lenz, M Repas-Humpe, J Oldenburg, et al.
Clinical Genetics|April 1, 1995
Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosisA Pekrun, B A Neubauer, S W Eber, et al.
European Journal of Pediatrics|November 1, 1985
Generalised glucosephosphate isomerase (GPI) deficiency causing haemolytic anaemia, neuromuscular symptoms and impairment of granulocytic function: a new syndrome due to a new stable GPI variant with diminished specific activity (GPI Homburg)W Schröter, S W Eber, A Bardosi, et al.
Human Genetics|January 1, 1984
Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 peopleS W Eber, M Dünnwald, G Heinemann, et al.
Biochemistry|January 28, 1999
Regulation of band 3 rotational mobility by ankyrin in intact human red cellsM R Cho, S W Eber, S C Liu, et al.
The British Journal of Surgery|December 29, 2007
Mode of splenectomy and immunogenicity of meningococcal vaccination in patients with hereditary spherocytosisG A Stoehr, J Luecken, S Zielen, et al.
Pediatric Transplantation|January 24, 2007
Favorable response of pediatric stem cell recipients to human protein C concentrate substitution for veno-occlusive diseaseS W Eber, T Gungor, A Veldman, et al.
Deutsche Medizinische Wochenschrift (1946)|April 2, 2009
[Prevention of infections and thromboses after splenectomy or because of functional loss of the spleen]M Engelhardt, P S Haas, C Theilacker, et al.
European Journal of Clinical Investigation|June 1, 1979
Hereditary deficiency of triosephosphate isomerase in four unrelated familiesS W Eber, M Dünnwald, B H Belohradsky, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
American Journal of Human Genetics|May 1, 1980
Characterization of a phosphoglycerate kinase deficiency variants not associated with hemolytic anemiaW K Krietsch, S W Eber, B Haas, et al.
European Journal of Pediatrics|December 14, 1999
Therapy-resistant haemarthros in a patient with factor VIII inhibitor: successful treatment with recombinant factor VIIaE Lenz, M Repas-Humpe, J Oldenburg, et al.
Clinical Genetics|April 1, 1995
Triosephosphate isomerase deficiency: biochemical and molecular genetic analysis for prenatal diagnosisA Pekrun, B A Neubauer, S W Eber, et al.
European Journal of Pediatrics|November 1, 1985
Generalised glucosephosphate isomerase (GPI) deficiency causing haemolytic anaemia, neuromuscular symptoms and impairment of granulocytic function: a new syndrome due to a new stable GPI variant with diminished specific activity (GPI Homburg)W Schröter, S W Eber, A Bardosi, et al.
Human Genetics|January 1, 1984
Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 peopleS W Eber, M Dünnwald, G Heinemann, et al.
Biochemistry|January 28, 1999
Regulation of band 3 rotational mobility by ankyrin in intact human red cellsM R Cho, S W Eber, S C Liu, et al.
The British Journal of Surgery|December 29, 2007
Mode of splenectomy and immunogenicity of meningococcal vaccination in patients with hereditary spherocytosisG A Stoehr, J Luecken, S Zielen, et al.
Pediatric Transplantation|January 24, 2007
Favorable response of pediatric stem cell recipients to human protein C concentrate substitution for veno-occlusive diseaseS W Eber, T Gungor, A Veldman, et al.
Deutsche Medizinische Wochenschrift (1946)|April 2, 2009
[Prevention of infections and thromboses after splenectomy or because of functional loss of the spleen]M Engelhardt, P S Haas, C Theilacker, et al.
European Journal of Clinical Investigation|June 1, 1979
Hereditary deficiency of triosephosphate isomerase in four unrelated familiesS W Eber, M Dünnwald, B H Belohradsky, et al.
Pageof 5