Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Galacteros

Showing results (51-60 of 187) with videos related to

Pageof 19
Sort By:
European Journal of Pediatrics|March 1, 1993
Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell DiseaseM de Montalembert, P Beauvais, D Bachir, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
[Epidemiologic study of hemoglobinopathies in the Congo in 2,257 newborn infants]M Djembo-Taty, M Tchiloemba, F Galacteros, et al.
Molecular Pharmacology|November 1, 1984
Inhibition of erythrocyte sickling by thiol reagentsM C Garel, C Domenget, F Galacteros, et al.
Hemoglobin|January 1, 1989
Inhibition of oxygen-linked anion binding in Hb Camperdown [alpha 2 beta 2(104)(G6)Arg----Ser]J Kister, J Barbadjian, Y Blouquit, et al.
American Journal of Hematology|December 1, 1989
Hemoglobin Villejuif [beta 123(H1) Thr----Ile]: a new variant found in coincidence with polycythemia veraH Wajcman, A Mrad, Y Blouquit, et al.
Hemoglobin|November 1, 1994
Two new alpha chain variants found during glycated hemoglobin screening: Hb Tatras [alpha 7(A5)Lys-->Asn] and HB Lisbon [alpha 23(B4)Glu-->Asp]H Wajcman, M Bost, Y Blouquiit, et al.
The European Respiratory Journal|December 24, 1998
Pulmonary function in sickle cell disease with or without acute chest syndromeF Santoli, F Zerah, N Vasile, et al.
Hemoglobin|January 1, 1988
First observation of Hb Montgomery [alpha 48(CD6)Leu----Arg] in TunisiaA Mrad, N Arous, R Kastally, et al.
The Biochemical Journal|August 15, 1988
Endogenous calcium in sickle cells does not activate polyphosphoinositide phospholipase CM D Rhoda, J C Sulpice, P Gascard, et al.
Revue De Pneumologie Clinique|January 1, 1985
[Familial polycythemia caused by high oxygen affinity hemoglobin. 2nd world case of hemoglobin J Providence]D Rafaillat, O Oules, G Vernet, et al.
Pageof 19

Showing results (51-60 of 187) with videos related to

Sort By:
Pageof 19
European Journal of Pediatrics|March 1, 1993
Cerebrovascular accidents in sickle cell disease. Risk factors and blood transfusion influence. French Study Group on Sickle Cell DiseaseM de Montalembert, P Beauvais, D Bachir, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
[Epidemiologic study of hemoglobinopathies in the Congo in 2,257 newborn infants]M Djembo-Taty, M Tchiloemba, F Galacteros, et al.
Molecular Pharmacology|November 1, 1984
Inhibition of erythrocyte sickling by thiol reagentsM C Garel, C Domenget, F Galacteros, et al.
Hemoglobin|January 1, 1989
Inhibition of oxygen-linked anion binding in Hb Camperdown [alpha 2 beta 2(104)(G6)Arg----Ser]J Kister, J Barbadjian, Y Blouquit, et al.
American Journal of Hematology|December 1, 1989
Hemoglobin Villejuif [beta 123(H1) Thr----Ile]: a new variant found in coincidence with polycythemia veraH Wajcman, A Mrad, Y Blouquit, et al.
Hemoglobin|November 1, 1994
Two new alpha chain variants found during glycated hemoglobin screening: Hb Tatras [alpha 7(A5)Lys-->Asn] and HB Lisbon [alpha 23(B4)Glu-->Asp]H Wajcman, M Bost, Y Blouquiit, et al.
The European Respiratory Journal|December 24, 1998
Pulmonary function in sickle cell disease with or without acute chest syndromeF Santoli, F Zerah, N Vasile, et al.
Hemoglobin|January 1, 1988
First observation of Hb Montgomery [alpha 48(CD6)Leu----Arg] in TunisiaA Mrad, N Arous, R Kastally, et al.
The Biochemical Journal|August 15, 1988
Endogenous calcium in sickle cells does not activate polyphosphoinositide phospholipase CM D Rhoda, J C Sulpice, P Gascard, et al.
Revue De Pneumologie Clinique|January 1, 1985
[Familial polycythemia caused by high oxygen affinity hemoglobin. 2nd world case of hemoglobin J Providence]D Rafaillat, O Oules, G Vernet, et al.
Pageof 19