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T Krusius

Showing results (81-90 of 105) with videos related to

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Thrombosis and Haemostasis|October 6, 2000
Single founder mutation (W380G) in type II protein C deficiency in FinlandA Levo, K Kuismanen, P Holopainen, et al.
Pediatric Hematology and Oncology|March 24, 1998
Multiple drug resistance mediated by P-glycoprotein is not a major factor in a slow response to therapy in childhood ALLJ Kanerva, M Tiirikainen, A Mäkipernaa, et al.
Gut|March 13, 2003
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's diseaseT Heliö, L Halme, M Lappalainen, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 18, 2003
Melanocortin-3-receptor gene variants in morbid obesityC Schalin-Jäntti, K Valli-Jaakola, L Oksanen, et al.
Pediatric Hematology and Oncology|February 24, 2001
Initial P-glycoprotein expression in childhood acute lymphoblastic leukemia: no evidence of prognostic impact in follow-upJ Kanerva, M I Tiirikainen, A Mäkipernaa, et al.
Journal of Clinical Microbiology|April 1, 1994
Geographical distribution of hepatitis C virus genotypes in blood donors: an international collaborative surveyF McOmish, P L Yap, B C Dow, et al.
The Journal of General Virology|May 1, 1995
Survey of major genotypes and subtypes of hepatitis C virus using RFLP of sequences amplified from the 5' non-coding regionF Davidson, P Simmonds, J C Ferguson, et al.
Vox Sanguinis|May 8, 1999
Blood transfusion in premature or young infants with polyagglutination and activation of the T antigenC P Engelfriet, H W Reesink, R G Strauss, et al.
The American Journal of Clinical Nutrition|February 16, 1999
Higher concentrations of serum transferrin receptor in children than in adultsM A Virtanen, L U Viinikka, M K Virtanen, et al.
Vox Sanguinis|August 16, 2006
Development of permanent national register of blood component use utilizing electronic hospital information systemsR Palo, T Ali-Melkkilä, R Hanhela, et al.
Pageof 11

Showing results (81-90 of 105) with videos related to

Sort By:
Pageof 11
Thrombosis and Haemostasis|October 6, 2000
Single founder mutation (W380G) in type II protein C deficiency in FinlandA Levo, K Kuismanen, P Holopainen, et al.
Pediatric Hematology and Oncology|March 24, 1998
Multiple drug resistance mediated by P-glycoprotein is not a major factor in a slow response to therapy in childhood ALLJ Kanerva, M Tiirikainen, A Mäkipernaa, et al.
Gut|March 13, 2003
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's diseaseT Heliö, L Halme, M Lappalainen, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 18, 2003
Melanocortin-3-receptor gene variants in morbid obesityC Schalin-Jäntti, K Valli-Jaakola, L Oksanen, et al.
Pediatric Hematology and Oncology|February 24, 2001
Initial P-glycoprotein expression in childhood acute lymphoblastic leukemia: no evidence of prognostic impact in follow-upJ Kanerva, M I Tiirikainen, A Mäkipernaa, et al.
Journal of Clinical Microbiology|April 1, 1994
Geographical distribution of hepatitis C virus genotypes in blood donors: an international collaborative surveyF McOmish, P L Yap, B C Dow, et al.
The Journal of General Virology|May 1, 1995
Survey of major genotypes and subtypes of hepatitis C virus using RFLP of sequences amplified from the 5' non-coding regionF Davidson, P Simmonds, J C Ferguson, et al.
Vox Sanguinis|May 8, 1999
Blood transfusion in premature or young infants with polyagglutination and activation of the T antigenC P Engelfriet, H W Reesink, R G Strauss, et al.
The American Journal of Clinical Nutrition|February 16, 1999
Higher concentrations of serum transferrin receptor in children than in adultsM A Virtanen, L U Viinikka, M K Virtanen, et al.
Vox Sanguinis|August 16, 2006
Development of permanent national register of blood component use utilizing electronic hospital information systemsR Palo, T Ali-Melkkilä, R Hanhela, et al.
Pageof 11