Zobrazeno 1 - 10
of 172
pro vyhledávání: '"R, Hafsia"'
Leucémie érythroblastique pure associée à un syndrome d’activation macrophagique : à propos d’un cas
Autor:
I. Bellagha, K. Mrad, N. E. H. Toumi, V. Saada, K. Boussetta, M. Becheur, R. Hafsia, I. Brini, A. Saad, S. Jarraya
Publikováno v:
Journal Africain du Cancer / African Journal of Cancer. 7:263-268
Il s’agit d’un enfant âge de 6 ans hospitalise pour une alteration de l’etat general avec une pâleur intense et une hepatosplenomegalie. Il n’a pas d’antecedents personnels ou familiaux et il n’existe pas de consanguinite. L’hemogramm
Autor:
Amina Bibi, R. Othmeni, B. Dakhlaoui, Hajer Siala, Latifa Jouini, Chaima Abdelhafidh Sahli, Mariem Becher, Taieb Messaoud, S. Hadj Fredj, Faida Ouali, F. Ouennich, N. Laaouini, R. Hafsia, Fattoum S, Nour El Houda Toumi, I. Ben Youssef
Publikováno v:
Molecular Biology Reports. 40:6205-6212
Beta-thalassemia is the most frequent hereditary blood disorder in Tunisia because of its geographic localization and history. This pathology is characterized by a complex multisystem process with genetic and biochemical interactions. The aim of this
Autor:
N, Ben Salah, W, El Borgi, F, Ben Lakhal, M, Ben Mansour, E, Gouider, Y, Gorgi, R, Bardi, B, Zoueri, R, Hafsia
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 21(6)
Evaluate the anti-erythrocyte and anti-HLA immunization rates in hemoglobinopathies.Cross-sectional study (October 2009-March 2010) on 83 patients followed for hemoglobinopathies. The irregular antibodies research is realized by two techniques: indir
Publikováno v:
Annales de cardiologie et d'angeiologie. 64(4)
Atrial fibrillation can expose to thrombo-embolic complications. Many biomarkers have been tested to refine the stratification of thrombo-embolic risk. The study aim was to assess the interest of the d-dimer testing in this pathology. We conducted a
Autor:
N, Ben Salah, W, El Borgi, H, Aounallah Skhiri, F, Ben Lakhal, H, Mouelhi, B, Zoueri, E, Gouider, R, Hafsia
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 20(4)
In Tunisia, red blood cells (RBC) transfusion joins in a statutory frame but remains subject to failures because of the misunderstanding of legislation and regulations. Our purpose is to estimate the knowledge of the medical staff in the immunologica
Autor:
N, Ben Salah, W, El Borgi, A, Chelbi, F, Ben Lakhal, E, Gouider, H, Aounallah Skhiri, R, Hafsia
Publikováno v:
Pathologie-biologie. 62(6)
The determination of the cellular lineage in acute leukemia is a crucial step in the diagnosis and the later therapeutic conduct. In Tunisia, emerging country, some cases of acute leukemias are still treated on the basis of an only cytologic study be
Publikováno v:
Pathologie-biologie. 61(2)
A previous study on G6PD deficiency carried out on Tunisian population, led to the finding of seven different mutations with the prevalence of G6PD A- variant. This present study reports 23 new unrelated deficient subjects studied at the molecular le
Publikováno v:
Archives de l'Institut Pasteur de Tunis. 83(1-4)
Acute promyelocytic leukaemia (AML3) is characterized by particular clinical and biological features. We report the cytology and the immunophenotype of 14 AML3 from which 3 were AML3v. A double negativity of HLA-DR and CD34 is found in 12 cases and a
Publikováno v:
Pathologie Biologie
Pathologie Biologie, Elsevier Masson, 2008, 56 (5), pp.260-267. ⟨10.1016/j.patbio.2007.08.009⟩
Pathologie Biologie, Elsevier Masson, 2008, 56 (5), pp.260-267. ⟨10.1016/j.patbio.2007.08.009⟩
International audience; Screening of G6PD deficiency was carried out on 79 unrelated subjects (32 females and 47 males), all coming from out consultation. DNA from deficient subject (11 females and 30 males) was analyzed for the presence of G6PD muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::385c782f63f7ef59d47a3021d7874052
https://hal-riip.archives-ouvertes.fr/pasteur-01375220
https://hal-riip.archives-ouvertes.fr/pasteur-01375220
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 12(4)
In this work, we proposed to evaluate prevalences of hepatitis B and C viruses and Parvovirus B19 among 70 Tunisian haemophiliacs treated with clotting factors imported from Europe and/or locally produced cryoprecipitate; among them 6 (8.6%) are know