Serologic and molecular characterization of weak D type 29 von Ouchari, Mouna, Srivastava, Kshitij, Döscher, Andrea, Conradi, Roland, Jemni Yacoub, Saloua, Wagner, Franz Friedrich, Flegel, Willy Albert

Volltext

Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia von Ouchari, Mouna, Srivastava, Kshitij, Romdhane, Houda, Jemni Yacoub, Saloua, Flegel, Willy Albert

Volltext

Antiphospholipid antibodies in autoimmune thyroid diseases von Mankaï, Amani, Melayah, Sarra, Bousetta, Syrine, Ghozzi, Mariem, Yacoub‐Jemni, Saloua, Ghedira, Ibtissem

Volltext

RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in Tunisia von Kacem, Narjes, Chakroun, Tahar, Moussa, Hajer, Abdelkefi, Saïda, Houissa, Betoul, Chiaroni, Jacques, Jemni Yacoub, Saloua

Volltext

RHD genotyping and its implication in transfusion practice von Sassi, Awatef, Ouchari, Mouna, Houissa, Batoul, Romdhane, Houda, Abdelkefi, Saida, Chakroun, Taher, Jemni Yacoub, Saloua

Volltext

Molecular background of D-negative phenotype in the Tunisian population von Moussa, H., Tsochandaridis, M., Chakroun, T., Jridi, S., Abdelneji, B., Hmida, S., Silvy, M., Bailly, P., Gabert, J., Levy-Mozziconacci, A., Jemni-Yacoub, Saloua

Volltext

(C)ce(s) haplotype screening in Tunisian blood donors von Moussa, Hajer, Ghommen, Néjiba, Romdhane, Houda, Abdelkefi, Saadia, Chakroun, Taher, Houissa, Batoul, Jemni, Saloua Yacoub

Volltext

Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus von Amara, Abdelbasset, Ben Charfeddine, Ilhem, Ghédir, Houda, Mamaï, Ons, Jemni-Yacoub, Saloua, Chaieb, Larbi, Saad, Ali, Chadli-Chaieb, Molka, Gribaa, Moez

Volltext

Chrysin, a natural and biologically active flavonoid suppresses tumor growth of mouse B16F10 melanoma cells: In vitro and In vivo study von Sassi, Aïcha, Maatouk, Mouna, El gueder, Dorra, Bzéouich, Imen Mokdad, Abdelkefi-Ben Hatira, Saïda, Jemni-Yacoub, Saloua, Ghedira, Kamel, Chekir-Ghedira, Leila

Volltext

IgA anti-beta-2 glycoprotein I antibodies in chronic hepatitis C von Melayah, Sarra, Kallala, Ouafa, Ben Ahmed, Mariem, Fodha, Imen, Yacoub Jemni, Saloua, Ghedira, Ibtissem, Mankaï, Amani

Volltext

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29 von Silvy, Monique, Beley, Sophie, Peyrard, Thierry, Ouchari, Mouna, Abdelkefi, Saadia, Jemni Yacoub, Saloua, Chiaroni, Jacques, Bailly, Pascal

Volltext

Leucocyte cytokines dominate platelet cytokines overtime in non-leucoreduced platelet components von Aloui, Chaker, Chakroun, Tahar, Prigent, Antoine, Jemni-Yacoub, Saloua, Cognasse, Fabrice, Laradi, Sandrine, Garraud, Olivier

Volltext

Weak D in the Tunisian population von Ouchari, Mouna, Romdhane, Houda, Chakroun, Taher, Abdelkefi, Saida, Houissa, Batoul, Hmida, Slama, Yacoub, Saloua Jemni

Volltext

Are polymorphisms of the immunoregulatory factor CD40LG implicated in acute transfusion reactions? von Aloui, Chaker, Sut, Caroline, Prigent, Antoine, Fagan, Jocelyne, Cognasse, Fabrice, Granados-Herbepin, Viviana, Touraine, Renaud, Pozzetto, Bruno, Aouni, Mahjoub, Fendri, Chedlia, Hassine, Mohsen, Chakroun, Tahar, Jemni-Yacoub, Saloua, Garraud, Olivier, Laradi, Sandrine

Volltext

Short duplication within the RHCE gene associated with an in cis deleted RHD causing a R h null amorph phenotype in an immunized pregnant woman with anti‐ R h29 von Silvy, Monique, Beley, Sophie, Peyrard, Thierry, Ouchari, Mouna, Abdelkefi, Saadia, Jemni Yacoub, Saloua, Chiaroni, Jacques, Bailly, Pascal

Volltext

Molecular genetic diagnosis of Tunisian Glanzmann thrombasthenia patients reveals a common nonsense mutation in the ITGA2B gene that seems to be specific for the studied population von Aloui, Chaker, Chakroun, Tahar, Granados, Viviana, Jemni-Yacoub, Saloua, Fagan, Jocelyne, Khelif, Abderrahim, Kahloul, Najoua, Hammami, Sabeur, Chkioua, Latifa, Barlier, Céline, Cognasse, Fabrice, Laradi, Sandrine, Garraud, Olivier

Volltext

Paternal RHD zygosity determination in Tunisians: evaluation of three molecular tests von Kacem, Narjes, Jemni-Yacoub, Saloua, Chiaroni, Jacques, Bailly, Pascal, Silvy, Monique

Volltext

(C)ces haplotype screening in Tunisian blood donors von Moussa, Hajer, Ghommen, Néjiba, Romdhane, Houda, Abdelkefi, Saadia, Chakroun, Taher, Houissa, Batoul, Jemni, Saloua Yacoub

Volltext

Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies von Hamadou, Walid S., Bourdon, Violaine, Gaildrat, Pascaline, Besbes, Sawsen, Fabre, Aurélie, Youssef, Yosra B., Regaieg, Haifa, Laatiri, Mohamed A., Eisinger, François, Mari, Véronique, Gesta, Paul, Dreyfus, Hélène, Bonadona, Valérie, Dugast, Catherine, Zattara, Hélène, Faivre, Laurence, Jemni, Saloua Yacoub, Noguchi, Testsuro, Khélif, Abderrahim, Sobol, Hagay, Soua, Zohra

Volltext

RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in T unisia von Kacem, Narjes, Chakroun, Tahar, Moussa, Hajer, Abdelkefi, Saïda, Houissa, Betoul, Chiaroni, Jacques, Jemni Yacoub, Saloua

Volltext