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R Girot

Showing results (151-160 of 195) with videos related to

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European Journal of Pediatrics|April 1, 1986
Neocytopheresis: a new approach for the transfusion of patients with thalassaemia majorP Triadou, R Girot, D Rebibo, et al.
The Journal of Pediatrics|August 1, 1993
Iron overload in children receiving prolonged parenteral nutritionM Ben Hariz, O Goulet, S De Potter, et al.
Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology : Official Publication of the International Retrovirology Association|August 26, 1998
Serum ferritin, desferrioxamine, and evolution of HIV-1 infection in thalassemic patientsY Salhi, D Costagliola, P Rebulla, et al.
Blood|October 15, 1993
Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in childrenM de Montalembert, M Maier-Redelsperger, R Girot, et al.
The New England Journal of Medicine|March 24, 1983
Cellular immune deficiency in two siblings with hereditary orotic aciduriaR Girot, M Hamet, J L Perignon, et al.
The Journal of Pediatrics|May 1, 1983
Diet-responsive proconvertin (factor VII) deficiency in homocystinuriaA Munnich, J M Saudubray, M D Dautzenberg, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1989
No evidence for a defect in growth hormone binding to liver membranes in thalassemia majorM C Postel-Vinay, R Girot, J Leger, et al.
Archives of Disease in Childhood|March 1, 1990
Partial splenectomy in homozygous beta thalassaemiaM de Montalembert, R Girot, Y Revillon, et al.
Hemoglobin|March 11, 1998
Hb Godavari [alpha 95(G2)Pro-->Thr]: a neutral amino acid substitution in the alpha 1 beta 2 interface that modifies the electrophoretic mobility of hemoglobinH Wajcman, J Kister, J Riou, et al.
Transfusion|July 1, 1992
Prevalence of markers for human immunodeficiency virus types 1 and 2, human T-lymphotropic virus type I, cytomegalovirus, and hepatitis B and C virus in multiply transfused thalassemia patients. The French Study Group On ThalassaemiaM de Montalembert, D G Costagliola, J J Lefrère, et al.
Pageof 20

Showing results (151-160 of 195) with videos related to

Sort By:
Pageof 20
European Journal of Pediatrics|April 1, 1986
Neocytopheresis: a new approach for the transfusion of patients with thalassaemia majorP Triadou, R Girot, D Rebibo, et al.
The Journal of Pediatrics|August 1, 1993
Iron overload in children receiving prolonged parenteral nutritionM Ben Hariz, O Goulet, S De Potter, et al.
Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology : Official Publication of the International Retrovirology Association|August 26, 1998
Serum ferritin, desferrioxamine, and evolution of HIV-1 infection in thalassemic patientsY Salhi, D Costagliola, P Rebulla, et al.
Blood|October 15, 1993
Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in childrenM de Montalembert, M Maier-Redelsperger, R Girot, et al.
The New England Journal of Medicine|March 24, 1983
Cellular immune deficiency in two siblings with hereditary orotic aciduriaR Girot, M Hamet, J L Perignon, et al.
The Journal of Pediatrics|May 1, 1983
Diet-responsive proconvertin (factor VII) deficiency in homocystinuriaA Munnich, J M Saudubray, M D Dautzenberg, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1989
No evidence for a defect in growth hormone binding to liver membranes in thalassemia majorM C Postel-Vinay, R Girot, J Leger, et al.
Archives of Disease in Childhood|March 1, 1990
Partial splenectomy in homozygous beta thalassaemiaM de Montalembert, R Girot, Y Revillon, et al.
Hemoglobin|March 11, 1998
Hb Godavari [alpha 95(G2)Pro-->Thr]: a neutral amino acid substitution in the alpha 1 beta 2 interface that modifies the electrophoretic mobility of hemoglobinH Wajcman, J Kister, J Riou, et al.
Transfusion|July 1, 1992
Prevalence of markers for human immunodeficiency virus types 1 and 2, human T-lymphotropic virus type I, cytomegalovirus, and hepatitis B and C virus in multiply transfused thalassemia patients. The French Study Group On ThalassaemiaM de Montalembert, D G Costagliola, J J Lefrère, et al.
Pageof 20