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Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|August 25, 2018
How to mitigate the risk of inducing transfusion-associated adverse reactionsO Garraud, F Cognasse, S Laradi, et al.Frontiers in Immunology|December 15, 2016
Transfusion as an Inflammation Hit: Knowns and UnknownsOlivier Garraud, S Tariket, C Sut, et al.Pathologie-Biologie|November 15, 2011
Mucopolysaccharidosis IVA within Tunisian patients: Confirmation of the two novel GALNS gene mutationsS Khedhiri, L Chkioua, H Bouzidi, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1996
[Infantile visceral leishmaniasis: difficult diagnosis in cases complicated by hemophagocytosis]A Nadrid, H Pousse, S Laradi-Chebil, et al.Archives Francaises De Pediatrie|December 1, 1992
[Enzymatic and molecular studies in a case of hepato-erythropoietic porphyria. Homozygote form of type familial cutaneous porphyria]H de Verneuil, F Moreau-Gaudry, S Laradi, et al.BMC Medical Genetics|May 26, 2020
The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patientsL Chkioua, O Grissa, N Leban, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian familiesS Laradi, T Tukel, M Erazo, et al.Molecular Genetics and Metabolism|December 28, 2005
Mucopolysaccharidosis type IV: N-acetylgalactosamine-6-sulfatase mutations in Tunisian patientsS Laradi, T Tukel, S Khediri, et al.Annales De Biologie Clinique|April 19, 2003
[Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis]A H Khelil, S Laradi, S Ferchichi, et al.Pathologie-Biologie|January 8, 2008
[Molecular analysis of the p.Asn 370 Ser mutation in Gaucher disease]A Dandana, S Ferchichi, S Ben Khelifa, et al.Pageof 3