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Serologic and molecular characterization of weak D type 29

Transfusion (Philadelphia, Pa.), 2017-10, Vol.57 (10), p.2542-2544

2017

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Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia

Transfusion (Philadelphia, Pa.), 2018-02, Vol.58 (2), p.306-312

2018

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Antiphospholipid antibodies in autoimmune thyroid diseases

Journal of clinical laboratory analysis, 2022-12, Vol.36 (12), p.e24788-n/a

2022

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RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in Tunisia

Transfusion medicine (Oxford, England), 2012-10, Vol.22 (5), p.362-366

2012

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RHD genotyping and its implication in transfusion practice

Transfusion and apheresis science, 2014-12, Vol.51 (3), p.59-63

2014

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(C)ce(s) haplotype screening in Tunisian blood donors

Blood transfusion = Trasfusione del sangue, 2014-07, Vol.12 (3), p.405

2014

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Molecular background of D-negative phenotype in the Tunisian population

Transfusion medicine (Oxford, England), 2012-06, Vol.22 (3), p.192-198

2012

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Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus

Iranian journal of public health, 2015-03, Vol.44 (3), p.396-403

2015

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Chrysin, a natural and biologically active flavonoid suppresses tumor growth of mouse B16F10 melanoma cells: In vitro and In vivo study

Chemico-biological interactions, 2018-03, Vol.283, p.10-19

2018

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IgA anti-beta-2 glycoprotein I antibodies in chronic hepatitis C

Arab journal of gastroenterology, 2022-02, Vol.23 (1), p.26-31

2022

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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

Transfusion (Philadelphia, Pa.), 2015-06, Vol.55 (6pt2), p.1407-1410

2015

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Leucocyte cytokines dominate platelet cytokines overtime in non-leucoreduced platelet components

Blood transfusion = Trasfusione del sangue, 2018-01, Vol.16 (1), p.63-72

2018

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Weak D in the Tunisian population

Blood transfusion = Trasfusione del sangue, 2015-04, Vol.13 (2), p.295-301

2015

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Are polymorphisms of the immunoregulatory factor CD40LG implicated in acute transfusion reactions?

Scientific reports, 2014-11, Vol.4 (1), p.7239-7239, Article 7239

2014

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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

Transfusion (Philadelphia, Pa.), 2015-06, Vol.55 (6pt2), p.1407-1410

2015

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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

Blood coagulation & fibrinolysis, 2018-12, Vol.29 (8), p.689-696

2018

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Paternal RHD zygosity determination in Tunisians: evaluation of three molecular tests

Blood transfusion = Trasfusione del sangue, 2015-01, Vol.13 (1), p.59-65

2015

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(C)ces haplotype screening in Tunisian blood donors

Blood transfusion = Trasfusione del sangue, 2014-07, Vol.12 (3), p.405-409

2014

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Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies

Annals of hematology, 2016-06, Vol.95 (7), p.1043-1050

2016

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RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in T unisia

Transfusion medicine (Oxford, England), 2012-10, Vol.22 (5), p.362-366

2012

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Fetal RhD genotyping by real time quantitative PCR in maternal plasma of RhD-negative pregnant women from the Sahel of Tunisia

Annales de biologie clinique (Paris), 2012-11, Vol.70 (6), p.683-688

2012

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Molecular study of the perforin gene in familial hematological malignancies

Hereditary cancer in clinical practice, 2011-09, Vol.9 (1), p.9-9, Article 9

2011

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Perforin-1 does not appear to be associated with familial hematological malignancies

Hereditary cancer in clinical practice, 2011-09, Vol.9 (1)

2011

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Seroepidemiological survey of rickettsial infections among blood donors in central Tunisia

Transactions of the Royal Society of Tropical Medicine and Hygiene, 1995-05, Vol.89 (3), p.266-268

1995

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Serologic and molecular characterization of weak D type 29

Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia

Antiphospholipid antibodies in autoimmune thyroid diseases

RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in Tunisia

RHD genotyping and its implication in transfusion practice

(C)ce(s) haplotype screening in Tunisian blood donors

Molecular background of D-negative phenotype in the Tunisian population

Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus

Chrysin, a natural and biologically active flavonoid suppresses tumor growth of mouse B16F10 melanoma cells: In vitro and In vivo study

IgA anti-beta-2 glycoprotein I antibodies in chronic hepatitis C

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

Leucocyte cytokines dominate platelet cytokines overtime in non-leucoreduced platelet components

Weak D in the Tunisian population

Are polymorphisms of the immunoregulatory factor CD40LG implicated in acute transfusion reactions?

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

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

Paternal RHD zygosity determination in Tunisians: evaluation of three molecular tests

(C)ces haplotype screening in Tunisian blood donors

Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies

RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in T unisia

Fetal RhD genotyping by real time quantitative PCR in maternal plasma of RhD-negative pregnant women from the Sahel of Tunisia

Molecular study of the perforin gene in familial hematological malignancies

Perforin-1 does not appear to be associated with familial hematological malignancies

Seroepidemiological survey of rickettsial infections among blood donors in central Tunisia

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