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F Galacteros

Showing results (111-120 of 187) with videos related to

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Nouvelle Revue Francaise D'Hematologie|January 1, 1986
[Abnormal hemoglobins screened in Tunisia]A Blibech, A Mrad, A Belhas, et al.
American Journal of Hematology|October 1, 1989
Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in TunisiaA Mrad, J Kister, C Feo, et al.
Chest|May 16, 2000
Acute chest syndrome in adults with sickle cell diseaseB Maitre, A Habibi, F Roudot-Thoraval, et al.
Hemoglobin|January 1, 1989
Structure-function of Hb Marseille-Long Island [alpha 2 beta 2 N-methionyl-2(NA2) His----Pro]B Bohn, G Craescu, J Kister, et al.
FEBS Letters|April 6, 1981
Hemoglobin Saint Mandé beta 102 (G4) asn replaced by tyr: a new low oxygen affinity variantN Arous, F Braconnier, J Thillet, et al.
Annals of Hematology|May 1, 1993
Comparison of the protein and DNA approaches for the characterization of a beta-globin chain variant, hemoglobin Cocody [beta 21 (B3) Asp--->Asn], in a Caucasian patientP Aguilar-Martinez, F Galacteros, J F Schved, et al.
Seminars in Arthritis and Rheumatism|January 8, 2008
Characteristics and outcome of connective tissue diseases in patients with sickle-cell disease: report of 30 casesM Michel, A Habibi, B Godeau, et al.
Human Genetics|September 1, 1986
Hemoglobin abnormalities. An evaluation on new-born infants and their mothers in a maternity unit close to Brazzaville (P.R. Congo)M Lallemant, F Galacteros, S Lallemant-Lecoeur, et al.
Hemoglobin|January 1, 1992
HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee familyS Abbes, A M'Rad, P A Fitzgerald, et al.
Biorheology|January 1, 1989
Filterability of sickle cells as a function of pO2: role of physico-chemical factorsA Kraiem, C T Craescu, F Galacteros, et al.
Pageof 19

Showing results (111-120 of 187) with videos related to

Sort By:
Pageof 19
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
[Abnormal hemoglobins screened in Tunisia]A Blibech, A Mrad, A Belhas, et al.
American Journal of Hematology|October 1, 1989
Hemoglobin Athens-Georgia [alpha 2 beta 2 40(C6)Arg----Lys] in association with beta 0-thalassemia in TunisiaA Mrad, J Kister, C Feo, et al.
Chest|May 16, 2000
Acute chest syndrome in adults with sickle cell diseaseB Maitre, A Habibi, F Roudot-Thoraval, et al.
Hemoglobin|January 1, 1989
Structure-function of Hb Marseille-Long Island [alpha 2 beta 2 N-methionyl-2(NA2) His----Pro]B Bohn, G Craescu, J Kister, et al.
FEBS Letters|April 6, 1981
Hemoglobin Saint Mandé beta 102 (G4) asn replaced by tyr: a new low oxygen affinity variantN Arous, F Braconnier, J Thillet, et al.
Annals of Hematology|May 1, 1993
Comparison of the protein and DNA approaches for the characterization of a beta-globin chain variant, hemoglobin Cocody [beta 21 (B3) Asp--->Asn], in a Caucasian patientP Aguilar-Martinez, F Galacteros, J F Schved, et al.
Seminars in Arthritis and Rheumatism|January 8, 2008
Characteristics and outcome of connective tissue diseases in patients with sickle-cell disease: report of 30 casesM Michel, A Habibi, B Godeau, et al.
Human Genetics|September 1, 1986
Hemoglobin abnormalities. An evaluation on new-born infants and their mothers in a maternity unit close to Brazzaville (P.R. Congo)M Lallemant, F Galacteros, S Lallemant-Lecoeur, et al.
Hemoglobin|January 1, 1992
HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee familyS Abbes, A M'Rad, P A Fitzgerald, et al.
Biorheology|January 1, 1989
Filterability of sickle cells as a function of pO2: role of physico-chemical factorsA Kraiem, C T Craescu, F Galacteros, et al.
Pageof 19