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R Ducrocq

Showing results (21-30 of 59) with videos related to

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Hemoglobin|May 21, 1999
A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobinS Zertal-Zidani, T Merghoub, R Ducrocq, et al.
Diabete & Metabolisme|December 1, 1984
Haemoglobinopathies, malaria, and other interferences with HBA1 assessmentC Eberentz-Lhomme, R Ducrocq, S Intrator, et al.
Diabetologia|December 1, 1984
Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatographyC Eberentz-Lhomme, R Ducrocq, S Intrator, et al.
Thrombosis and Haemostasis|September 1, 1996
Increased procoagulant activity of red blood cells from patients with homozygous sickle cell disease and beta-thalassemiaD Helley, A Eldor, R Girot, et al.
Analytical Biochemistry|May 15, 1996
Perfusion chromatography on reversed-phase column allows fast analysis of human globin chainsH Wajcman, R Ducrocq, J Riou, et al.
Archives De L'Institut Pasteur De Tunis|July 1, 1987
[A case of hemoglobin D Punjab in Tunisia. Characterization and structural study]F Guemira, F Hajji, M Sellami, et al.
Cytometry|July 17, 1998
New method for quantitative determination of fetal hemoglobin-containing red blood cells by flow cytometry: application to sickle-cell diseaseJ M Navenot, T Merghoub, R Ducrocq, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 9, 2001
[Neonatal screening for sickle cell anemia: evaluation of a five-year experience in an area of northern Paris]R Ducrocq, M Benkerrou, L Brahimi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 27, 2009
[Announcing the diagnosis of sickle cell disease in a newborn to the parents]A Niakaté, F Cavazza, A Perrin, et al.
British Journal of Haematology|November 1, 1995
A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patientF Morlé, A Francina, R Ducrocq, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Hemoglobin|May 21, 1999
A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobinS Zertal-Zidani, T Merghoub, R Ducrocq, et al.
Diabete & Metabolisme|December 1, 1984
Haemoglobinopathies, malaria, and other interferences with HBA1 assessmentC Eberentz-Lhomme, R Ducrocq, S Intrator, et al.
Diabetologia|December 1, 1984
Haemoglobinopathies: a pitfall in the assessment of glycosylated haemoglobin by ion-exchange chromatographyC Eberentz-Lhomme, R Ducrocq, S Intrator, et al.
Thrombosis and Haemostasis|September 1, 1996
Increased procoagulant activity of red blood cells from patients with homozygous sickle cell disease and beta-thalassemiaD Helley, A Eldor, R Girot, et al.
Analytical Biochemistry|May 15, 1996
Perfusion chromatography on reversed-phase column allows fast analysis of human globin chainsH Wajcman, R Ducrocq, J Riou, et al.
Archives De L'Institut Pasteur De Tunis|July 1, 1987
[A case of hemoglobin D Punjab in Tunisia. Characterization and structural study]F Guemira, F Hajji, M Sellami, et al.
Cytometry|July 17, 1998
New method for quantitative determination of fetal hemoglobin-containing red blood cells by flow cytometry: application to sickle-cell diseaseJ M Navenot, T Merghoub, R Ducrocq, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 9, 2001
[Neonatal screening for sickle cell anemia: evaluation of a five-year experience in an area of northern Paris]R Ducrocq, M Benkerrou, L Brahimi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 27, 2009
[Announcing the diagnosis of sickle cell disease in a newborn to the parents]A Niakaté, F Cavazza, A Perrin, et al.
British Journal of Haematology|November 1, 1995
A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patientF Morlé, A Francina, R Ducrocq, et al.
Pageof 6