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S W Eber

Showing results (1-10 of 47) with videos related to

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Klinische Padiatrie|July 1, 1991
[Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]S W Eber
Kinderkrankenschwester : Organ Der Sektion Kinderkrankenpflege|April 1, 1997
[Anemias in children]S W Eber
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1989
[Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia]W Schröter, S W Eber
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1992
[Diagnosis and therapy of anemia in childhood. Part 2. Hemolytic anemia and anemia in the newborn infant]S W Eber, W Schröter
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1992
[Diagnosis and therapy of anemia in childhood. Part 1. Differential diagnosis, hypoplastic anemia, thalassemia]S W Eber, W Schröter
Therapeutische Umschau. Revue Therapeutique|February 3, 2006
[Red cell membrane defects]S W Eber, A R Huber
Biochimica Et Biophysica Acta|July 10, 1980
The isolation and characterization of the multiple forms of human skeletal muscle triosephosphate isomeraseS W Eber, W K Krietsch
Clinical Neuropathology|March 1, 1985
Ultrastructural and histochemical abnormalities of skeletal muscle in a patient with a new variant (type Homburg) of glucosephosphate isomerase (GPI) deficiencyA Bardosi, S W Eber, U Roessmann
Blut|January 1, 1989
G6PD Avenches and G6PD Moosburg: biochemical and erythrocyte membrane characterizationA Pekrun, S W Eber, W Schröter
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1986
[Angelman syndrome]S W Eber, S Joost, M Gabriel
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Klinische Padiatrie|July 1, 1991
[Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity]S W Eber
Kinderkrankenschwester : Organ Der Sektion Kinderkrankenpflege|April 1, 1997
[Anemias in children]S W Eber
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1989
[Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia]W Schröter, S W Eber
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|June 1, 1992
[Diagnosis and therapy of anemia in childhood. Part 2. Hemolytic anemia and anemia in the newborn infant]S W Eber, W Schröter
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1992
[Diagnosis and therapy of anemia in childhood. Part 1. Differential diagnosis, hypoplastic anemia, thalassemia]S W Eber, W Schröter
Therapeutische Umschau. Revue Therapeutique|February 3, 2006
[Red cell membrane defects]S W Eber, A R Huber
Biochimica Et Biophysica Acta|July 10, 1980
The isolation and characterization of the multiple forms of human skeletal muscle triosephosphate isomeraseS W Eber, W K Krietsch
Clinical Neuropathology|March 1, 1985
Ultrastructural and histochemical abnormalities of skeletal muscle in a patient with a new variant (type Homburg) of glucosephosphate isomerase (GPI) deficiencyA Bardosi, S W Eber, U Roessmann
Blut|January 1, 1989
G6PD Avenches and G6PD Moosburg: biochemical and erythrocyte membrane characterizationA Pekrun, S W Eber, W Schröter
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1986
[Angelman syndrome]S W Eber, S Joost, M Gabriel
Pageof 5