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O Rudolphi

Showing results (1-10 of 19) with videos related to

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Lakartidningen|May 1, 1996
[Hereditary spherocytosis is more common than expected. Hemolysis, anemia and splenomegaly are among the symptoms]O Rudolphi, P Hörnsten
Scandinavian Journal of Haematology|March 1, 1983
Effects of intensive plasmapheresis on the haemostatic systemT Nilsson, O Rudolphi, B Cedergren
Scandinavian Journal of Urology and Nephrology|January 1, 1971
Oral creatinine loadingB Lindqvist, O Rudolphi, L Jacobsson
European Journal of Haematology|October 1, 1995
Inherited phosphofructokinase deficiency associated with hemolysis and exertional myopathyO Rudolphi, B Ek, G Ronquist
Annales Chirurgiae Et Gynaecologiae|January 1, 1977
Serum fibrinogen/fibrin degradation products in patients with ovarian carcinomaO Lalos, B Frankendal, O Rudolphi
American Journal of Hematology|March 1, 1995
Initiation codon mutation (ATG --> ATA) of the beta-globin gene causing beta-thalassemia in a Swedish familyB Landin, O Rudolphi, B Ek
Acta Oncologica (Stockholm, Sweden)|January 1, 1995
Myelodysplastic syndromes--a population-based study on transformation and survivalP Hörnsten, A Wahlin, O Rudolphi, et al.
Scandinavian Journal of Haematology|January 1, 1986
Double gammopathies: incidence and clinical course of 20 patientsT Nilsson, B Norberg, O Rudolphi, et al.
Journal of Internal Medicine|February 13, 2001
Familial phosphofructokinase deficiency is associated with a disturbed calcium homeostasis in erythrocytesG Ronquist, O Rudolphi, I Engström, et al.
Acta Medica Scandinavica|May 1, 1982
Melphalan-related leukemia in multiple myelomaA Wahlin, G Roos, O Rudolphi, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Lakartidningen|May 1, 1996
[Hereditary spherocytosis is more common than expected. Hemolysis, anemia and splenomegaly are among the symptoms]O Rudolphi, P Hörnsten
Scandinavian Journal of Haematology|March 1, 1983
Effects of intensive plasmapheresis on the haemostatic systemT Nilsson, O Rudolphi, B Cedergren
Scandinavian Journal of Urology and Nephrology|January 1, 1971
Oral creatinine loadingB Lindqvist, O Rudolphi, L Jacobsson
European Journal of Haematology|October 1, 1995
Inherited phosphofructokinase deficiency associated with hemolysis and exertional myopathyO Rudolphi, B Ek, G Ronquist
Annales Chirurgiae Et Gynaecologiae|January 1, 1977
Serum fibrinogen/fibrin degradation products in patients with ovarian carcinomaO Lalos, B Frankendal, O Rudolphi
American Journal of Hematology|March 1, 1995
Initiation codon mutation (ATG --> ATA) of the beta-globin gene causing beta-thalassemia in a Swedish familyB Landin, O Rudolphi, B Ek
Acta Oncologica (Stockholm, Sweden)|January 1, 1995
Myelodysplastic syndromes--a population-based study on transformation and survivalP Hörnsten, A Wahlin, O Rudolphi, et al.
Scandinavian Journal of Haematology|January 1, 1986
Double gammopathies: incidence and clinical course of 20 patientsT Nilsson, B Norberg, O Rudolphi, et al.
Journal of Internal Medicine|February 13, 2001
Familial phosphofructokinase deficiency is associated with a disturbed calcium homeostasis in erythrocytesG Ronquist, O Rudolphi, I Engström, et al.
Acta Medica Scandinavica|May 1, 1982
Melphalan-related leukemia in multiple myelomaA Wahlin, G Roos, O Rudolphi, et al.
Pageof 2