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Showing results (121-130 of 195) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 2, 2001
Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin geneA Magdelaine, E Verdy, F Coulet, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Improved oxygen delivery to tissues and iron chelator transport through the use of lysed and resealed red blood cells: a new perspective on Cooley's anemia therapyC Ropars, B Teisseire, G Avenard, et al.
Clinical Rheumatology|August 31, 2006
Unusual sites of Salmonella osteoarthritis in patients with sickle cell disease: two casesC Bachmeyer, W Ammouri, P M'Bappé, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1990
Platelet function in sickle cell disease during steady stateP Triadou, E Fonty, A S Ambrosio, et al.
The Journal of Urology|December 1, 1984
Recurrent hematuria in 4 white patients with sickle cell traitE Oksenhendler, B Bourbigot, F Desbazeille, et al.
Liver|April 21, 1998
Hepatitis C associated with Guillain-Barré syndromeF Lacaille, H Zylberberg, H Hagège, et al.
The American Journal of Medicine|July 1, 1991
Poor tolerance of zidovudine in an HIV-asymptomatic patient with alpha-thalassemiaD Vittecoq, E Delabesse, M Bary, et al.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
The British Journal of Dermatology|December 1, 2007
Sickle cell leg ulcers: a frequently disabling complication and a marker of severityM Halabi-Tawil, F Lionnet, R Girot, et al.
Biomedica Biochimica Acta|January 1, 1983
The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosisN Alloisio, E Dorleac, L Morle, et al.
Pageof 20

Showing results (121-130 of 195) with videos related to

Sort By:
Pageof 20
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 2, 2001
Deep vein thrombosis during enoxaparin prophylactic treatment in a young pregnant woman homozygous for factor V Leiden and heterozygous for the G127-->a mutation in the thrombomodulin geneA Magdelaine, E Verdy, F Coulet, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Improved oxygen delivery to tissues and iron chelator transport through the use of lysed and resealed red blood cells: a new perspective on Cooley's anemia therapyC Ropars, B Teisseire, G Avenard, et al.
Clinical Rheumatology|August 31, 2006
Unusual sites of Salmonella osteoarthritis in patients with sickle cell disease: two casesC Bachmeyer, W Ammouri, P M'Bappé, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1990
Platelet function in sickle cell disease during steady stateP Triadou, E Fonty, A S Ambrosio, et al.
The Journal of Urology|December 1, 1984
Recurrent hematuria in 4 white patients with sickle cell traitE Oksenhendler, B Bourbigot, F Desbazeille, et al.
Liver|April 21, 1998
Hepatitis C associated with Guillain-Barré syndromeF Lacaille, H Zylberberg, H Hagège, et al.
The American Journal of Medicine|July 1, 1991
Poor tolerance of zidovudine in an HIV-asymptomatic patient with alpha-thalassemiaD Vittecoq, E Delabesse, M Bary, et al.
Blood|June 1, 1985
The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1L Morlé, M Garbarz, N Alloisio, et al.
The British Journal of Dermatology|December 1, 2007
Sickle cell leg ulcers: a frequently disabling complication and a marker of severityM Halabi-Tawil, F Lionnet, R Girot, et al.
Biomedica Biochimica Acta|January 1, 1983
The genetic abnormalities involving red cell membrane protein 4.1 with or without elliptocytosisN Alloisio, E Dorleac, L Morle, et al.
Pageof 20