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S W Eber

Showing results (11-20 of 47) with videos related to

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Annals of Hematology|February 1, 1992
Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: a diagnostic tool for hereditary spherocytosisR Armbrust, S W Eber, W Schröter
Blut|August 1, 1985
Glucose-6-phosphate dehydrogenase (G6PD) Iserlohn and G6PD Regensburg: two new severe enzyme defects in German familiesS W Eber, M Gahr, W Schröter
The Journal of Pediatrics|September 1, 1990
Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysisS W Eber, R Armbrust, W Schröter
Klinische Padiatrie|September 29, 2001
[Antiinfectious prophylaxis in asplenia]S W Eber, B H Belohradsky, M Weiss
Annals of Hematology|February 1, 1992
Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis testS W Eber, A Pekrun, A Neufeldt, et al.
Annals of Hematology|August 1, 1993
Combined ankyrin and spectrin deficiency in hereditary spherocytosisA Pekrun, S W Eber, A Kuhlmey, et al.
Archives of Biochemistry and Biophysics|April 1, 1979
Multiple forms of human phosphoglycerate kinaseW K Krietsch, I U Freier, S W Eber
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1988
[Aplastic crises in hereditary spherocytosis]A Pekrun, H Eiffert, S W Eber, et al.
Acta Neuropathologica|January 1, 1990
Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiencyA Bardosi, S W Eber, M Hendrys, et al.
FEBS Letters|February 13, 1989
Structural basis for the high activation energy of spectrin self-associationS A Morris, S W Eber, W B Gratzer
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Annals of Hematology|February 1, 1992
Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: a diagnostic tool for hereditary spherocytosisR Armbrust, S W Eber, W Schröter
Blut|August 1, 1985
Glucose-6-phosphate dehydrogenase (G6PD) Iserlohn and G6PD Regensburg: two new severe enzyme defects in German familiesS W Eber, M Gahr, W Schröter
The Journal of Pediatrics|September 1, 1990
Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysisS W Eber, R Armbrust, W Schröter
Klinische Padiatrie|September 29, 2001
[Antiinfectious prophylaxis in asplenia]S W Eber, B H Belohradsky, M Weiss
Annals of Hematology|February 1, 1992
Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis testS W Eber, A Pekrun, A Neufeldt, et al.
Annals of Hematology|August 1, 1993
Combined ankyrin and spectrin deficiency in hereditary spherocytosisA Pekrun, S W Eber, A Kuhlmey, et al.
Archives of Biochemistry and Biophysics|April 1, 1979
Multiple forms of human phosphoglycerate kinaseW K Krietsch, I U Freier, S W Eber
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1988
[Aplastic crises in hereditary spherocytosis]A Pekrun, H Eiffert, S W Eber, et al.
Acta Neuropathologica|January 1, 1990
Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiencyA Bardosi, S W Eber, M Hendrys, et al.
FEBS Letters|February 13, 1989
Structural basis for the high activation energy of spectrin self-associationS A Morris, S W Eber, W B Gratzer
Pageof 5