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R Girot

Showing results (61-70 of 195) with videos related to

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Archives Francaises De Pediatrie|February 1, 1989
[Treatment of post-transfusion iron overload by deferoxamine]M de Montalembert, A Llados, T Hannedouche, et al.
Seminars in Hematology|October 1, 1995
Transfusion-dependent thalassemia: viral complications (epidemiology and follow-up)M de Montalembert, R Girot, B Mattlinger, et al.
Nouvelle Revue Francaise D'Hematologie; Blood Cells|January 1, 1977
[Blood and bone marrow cytology in the diagnosis of illnesses of excess. Forty observations of mucopolysaccharidosis, mucolipidosis and mannosidosis]A Cosson, P Maroteaux, J Tapon, et al.
European Journal of Haematology|September 1, 1993
Epidemiological and clinical study of sickle cell disease in France, French Guiana and AlgeriaM de Montalembert, M Guilloud-Bataille, J Feingold, et al.
British Journal of Haematology|May 1, 1992
Incidence of AIDS in HIV-1 infected thalassaemia patients. European and Mediterranean W.H.O. Working Group on Haemoglobinopathies and CooleycareD G Costagliola, R Girot, P Rebulla, et al.
European Journal of Haematology|February 28, 2002
Long-term administration of high-dose deferoxamine 2 days per week in thalassemic patientsI Hagège, A Becker, T Kerdaffrec, et al.
Sante Publique (Vandoeuvre-Les-Nancy, France)|February 10, 2000
[Contributions to the sociologic analysis of the impact of sickle cell disease on families from Northern Tunisia]R Hamza, S Fattoum, M Péchevis, et al.
Revue Neurologique|June 9, 2000
[Spinal cord compression secondary to extramedullary hematopoiesis in a patient with thalassemia]G Bruneteau, G Fénelon, A Khalil, et al.
Annals of Neurology|May 1, 1985
Neurological findings in triosephosphate isomerase deficiencyB T Poll-The, J Aicardi, R Girot, et al.
Human Genetics|February 1, 1988
Analysis of crossover type in the alpha -3.7 haplotype among sickle cell anemia patients from various parts of AfricaC Dodé, A Berth, J Rochette, et al.
Pageof 20

Showing results (61-70 of 195) with videos related to

Sort By:
Pageof 20
Archives Francaises De Pediatrie|February 1, 1989
[Treatment of post-transfusion iron overload by deferoxamine]M de Montalembert, A Llados, T Hannedouche, et al.
Seminars in Hematology|October 1, 1995
Transfusion-dependent thalassemia: viral complications (epidemiology and follow-up)M de Montalembert, R Girot, B Mattlinger, et al.
Nouvelle Revue Francaise D'Hematologie; Blood Cells|January 1, 1977
[Blood and bone marrow cytology in the diagnosis of illnesses of excess. Forty observations of mucopolysaccharidosis, mucolipidosis and mannosidosis]A Cosson, P Maroteaux, J Tapon, et al.
European Journal of Haematology|September 1, 1993
Epidemiological and clinical study of sickle cell disease in France, French Guiana and AlgeriaM de Montalembert, M Guilloud-Bataille, J Feingold, et al.
British Journal of Haematology|May 1, 1992
Incidence of AIDS in HIV-1 infected thalassaemia patients. European and Mediterranean W.H.O. Working Group on Haemoglobinopathies and CooleycareD G Costagliola, R Girot, P Rebulla, et al.
European Journal of Haematology|February 28, 2002
Long-term administration of high-dose deferoxamine 2 days per week in thalassemic patientsI Hagège, A Becker, T Kerdaffrec, et al.
Sante Publique (Vandoeuvre-Les-Nancy, France)|February 10, 2000
[Contributions to the sociologic analysis of the impact of sickle cell disease on families from Northern Tunisia]R Hamza, S Fattoum, M Péchevis, et al.
Revue Neurologique|June 9, 2000
[Spinal cord compression secondary to extramedullary hematopoiesis in a patient with thalassemia]G Bruneteau, G Fénelon, A Khalil, et al.
Annals of Neurology|May 1, 1985
Neurological findings in triosephosphate isomerase deficiencyB T Poll-The, J Aicardi, R Girot, et al.
Human Genetics|February 1, 1988
Analysis of crossover type in the alpha -3.7 haplotype among sickle cell anemia patients from various parts of AfricaC Dodé, A Berth, J Rochette, et al.
Pageof 20