Zobrazeno 1 - 10
of 57
pro vyhledávání: '"S. Jemni Yacoub"'
Autor:
B. Houissa, I. Jarrey, Mouna Ouchari, H. Romdhane, S. Abdelkefi, S. Jemni Yacoub, T. Chakroun
Publikováno v:
Transfusion Clinique et Biologique. 22:76-79
Background Tunisia was described to as genetically heterogenous. Besides the 1% native Berber, the genetically influence of the Europeans seems much larger than that of sub-Saharan populations. Due to their ethnic variability, blood group variants ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d8fb882033abda480888abd1de684be
https://doi.org/10.1016/j.tracli.2015.03.002
https://doi.org/10.1016/j.tracli.2015.03.002
Autor:
H. Amara, S. Jemni Yacoub, S. Abdelkefi, N. Souyeh, I. Jarrey, S. Belhedi, B. Houissa, L. Boughammoura, T. Chakroun, H. Romdhane, M. Bouslama
Publikováno v:
Transfusion Clinique et Biologique. 21:309-313
Resume But de l’etude Etudier le profil clinico-biologique des patients β-thalassemiques dans notre region, reflet de la qualite de leur prise en charge. Patients et methodes Etude retrospective (2010–2011) portant sur 26 patients beta-thalassem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e59a1b1bedee0cef4ea2e5fbc80b94f
https://doi.org/10.1016/j.tracli.2014.10.002
https://doi.org/10.1016/j.tracli.2014.10.002
Autor:
Hajer Moussa, Jean Gabert, T. Chakroun, Marthe Tsochandaridis, S. Abdelkefi, A. Levy, Narjes Kacem, S. Jemni Yacoub
Publikováno v:
Transfusion Clinique et Biologique. 21:320-323
Purpose of the study The aim of this study was to investigate RHD alleles among Tunisian blood donors with D-negative phenotype and positive for C and/or E antigen. Patients and methods A total of 100 D-negative and C/E+ samples were analyzed by RHD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f572191e27eb2dfcbb7e600a61edae7
https://doi.org/10.1016/j.tracli.2014.10.004
https://doi.org/10.1016/j.tracli.2014.10.004
Autor:
S. Jemni Yacoub, B. Houissa, Mouna Ouchari, S. Hmida, H. Romdhane, Saïda Abdelkefi, Christian Gabriel, Helene Polin, T. Chakroun
Publikováno v:
Transfusion Medicine. 23:245-249
Summary Background and Objectives D is the most immunogenic blood group antigen. About 1% of whites carry an altered RHD allele leading to quantitative or qualitative changes in the antigen D expression. T201R and F223V encoded by 602C>G and 667T>G a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b410a0da6310d361ab25db1378332517
https://doi.org/10.1111/tme.12037
https://doi.org/10.1111/tme.12037
Autor:
S. Jemni Yacoub, B. Houissa, S. Abdelkefi, T. Chakroun, H. Romdhane, I. Jerray, M. Bouslama, I. Jedidi
Publikováno v:
Immuno-analyse & Biologie Spécialisée. 28:115-119
Summary Allele and genotype frequencies of HPA-1 and HPA-2 systems in a Tunisian population were determined by polymerase chain reaction with sequence-specific primers (PCR-SSP) in 100 volunteer blood donors. The risk of allo-immunization in these sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64c88600d0e55ab6c555dcdb7c5a916e
https://doi.org/10.1016/j.immbio.2012.12.005
https://doi.org/10.1016/j.immbio.2012.12.005
Autor:
M. Bouslama, S. Abdelkefi, S. Hmida, T. Chakroun, I. Jerray, S. Jemni Yacoub, Mouna Ouchari, B. Houissa, S. Belhedi
Publikováno v:
Transfusion Clinique et Biologique. 20:35-39
Resume But de l’etude La determination du phenotype RhD est importante en medecine transfusionnelle. Toutefois, la complexite de l’expression de l’antigene D est a l’origine des discordances observees entre deux determinations serologiques et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b83bfd977a3a8d9980ea0d0a804c29b3
https://doi.org/10.1016/j.tracli.2012.11.002
https://doi.org/10.1016/j.tracli.2012.11.002
Publikováno v:
Transfusion medicine (Oxford, England). 25(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0739226a2b3d8de6ab013c8e233a397
https://pubmed.ncbi.nlm.nih.gov/26482434
https://pubmed.ncbi.nlm.nih.gov/26482434
Autor:
H, Romdhane, H, Amara, S, Abdelkefi, N, Souyeh, T, Chakroun, I, Jarrey, M, Bouslama, S, Belhedi, B, Houissa, L, Boughammoura, S, Jemni Yacoub
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 21(6)
To study the clinical and biological profile of β-thalassemic patients in our region, reflecting the quality of their care.A retrospective study (2010-2011) on 26 β-thalassemic patients followed in the pediatrics service at CHU Farhat Hached Sousse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::20c9486082ac24ddc0d7ff8ec941227f
https://pubmed.ncbi.nlm.nih.gov/25458984
https://pubmed.ncbi.nlm.nih.gov/25458984
Publikováno v:
Transfusion Medicine. 25:426-427
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::584a2a06ff5c6b7959de712f6c49fb87
https://doi.org/10.1111/tme.12254
https://doi.org/10.1111/tme.12254
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 21(1)
We report the case of a 56-year-old patient with blood group O+C-c+E-e+K-, followed for a myelodysplasic syndrome and treated by regular pheno-identical and compatible (RBCs) transfusion since December 2007. In June 2009, a positive crossmatch was fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52882220de4c68c49a77a5b60e74634b
https://pubmed.ncbi.nlm.nih.gov/24365172
https://pubmed.ncbi.nlm.nih.gov/24365172