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F Galacteros

Showing results (161-170 of 187) with videos related to

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Hemoglobin|January 1, 1987
Further characterization of Hb Henri Mondor or alpha 2 beta 2(26)(B8)Glu----ValJ Bardakdjian, N Arous, J Kister, et al.
Hemoglobin|January 1, 1986
Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndromeM D Rhoda, N Arous, M C Garel, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1994
[Transfusion and alloimmunization in sickle cell anemia patients]F Norol, J Nadjahi, D Bachir, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1985
[Abnormal hemoglobins identified in Martinique]N Monplaisir, F Galacteros, N Arous, et al.
Hemoglobin|January 1, 1987
A new case of Hb Little Rock [beta 143(H21)His----Gln], a high affinity variant. Study during pregnancyA Francina, C Lacombe, F Baklouti, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Endothelial cells and adhesion of red cells in diabetes and sickle cell anemia. Quantitative and qualitative aspects]J L Wautier, M P Wautier, C Guillam-Megnin, et al.
Hemoglobin|January 1, 1984
Two new cases of heterozygosity for hemoglobin Knossos alpha 2 beta 2 27 Ala----Ser detected in the French West Indies and AlgeriaF Galacteros, J D Garin, N Monplaisir, et al.
FEBS Letters|December 10, 1984
Hb Marseille [alpha 2 beta 2 N methionyl-2 (NA2) His----Pro]: a new beta chain variant having an extended N-terminusY Blouquit, N Arous, D Lena, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 26, 1998
Early glomerular dysfunction in patients with sickle cell anemiaF Schmitt, F Martinez, G Brillet, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 1, 1994
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygousF Galacteros, E Girodon, A M'Rad, et al.
Pageof 19

Showing results (161-170 of 187) with videos related to

Sort By:
Pageof 19
Hemoglobin|January 1, 1987
Further characterization of Hb Henri Mondor or alpha 2 beta 2(26)(B8)Glu----ValJ Bardakdjian, N Arous, J Kister, et al.
Hemoglobin|January 1, 1986
Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndromeM D Rhoda, N Arous, M C Garel, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1994
[Transfusion and alloimmunization in sickle cell anemia patients]F Norol, J Nadjahi, D Bachir, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1985
[Abnormal hemoglobins identified in Martinique]N Monplaisir, F Galacteros, N Arous, et al.
Hemoglobin|January 1, 1987
A new case of Hb Little Rock [beta 143(H21)His----Gln], a high affinity variant. Study during pregnancyA Francina, C Lacombe, F Baklouti, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Endothelial cells and adhesion of red cells in diabetes and sickle cell anemia. Quantitative and qualitative aspects]J L Wautier, M P Wautier, C Guillam-Megnin, et al.
Hemoglobin|January 1, 1984
Two new cases of heterozygosity for hemoglobin Knossos alpha 2 beta 2 27 Ala----Ser detected in the French West Indies and AlgeriaF Galacteros, J D Garin, N Monplaisir, et al.
FEBS Letters|December 10, 1984
Hb Marseille [alpha 2 beta 2 N methionyl-2 (NA2) His----Pro]: a new beta chain variant having an extended N-terminusY Blouquit, N Arous, D Lena, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 26, 1998
Early glomerular dysfunction in patients with sickle cell anemiaF Schmitt, F Martinez, G Brillet, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 1, 1994
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygousF Galacteros, E Girodon, A M'Rad, et al.
Pageof 19