Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Imen Boudrigua"'
Autor:
Nawel Trabelsi, Ghada Bouguerra, Faten Haddad, Monia Ouederni, Imen Darragi, Imen Boudrigua, Dorra Chaouachi, Mbarka Barmat, Chaker Fouzai, Mohamed Bejaoui, Samia Menif, Imen Kraiem, Salem Abbes
Publikováno v:
Cellular Physiology and Biochemistry, Vol 55, Iss 1, Pp 117-129 (2021)
Externí odkaz:
https://doaj.org/article/dfaaabcdd6f94502879de79c424c2da2
Autor:
Mohamed Bejaoui, Samia Menif, Mbarka Barmat, Salem Abbes, Imen Boudrigua, Imen Darragi, Imen Kraiem, Nawel Trabelsi, Dorra Chaouachi, Monia Ouederni, Faten Haddad, Ghada Bouguerra, Chaker Fouzai
Publikováno v:
Cellular Physiology and Biochemistry, Vol 55, Iss 1, Pp 117-129 (2021)
Background/Aims: Hereditary Spherocytosis (HS) is the most common erythrocyte membrane disorder causing hemolytic anemia. The wide heterogeneity of both clinical and laboratory manifestations of HS contributes to difficulties associated with the diag
Autor:
Naima Saidani, Emna Bouatrous, Houyem Ouragini, Amira Ayachi, Imen Kraiem, Imen Boudrigua, Ons Laabidi, Samia Menif, Dorra Chaouachi, Sana Zitouni, Salem Abbes, Mechaal Mourali
Publikováno v:
American journal of perinatology. 39(11)
This study was aimed to establish local reference values for hematological indices and hemoglobin (Hb) fractions in umbilical cord blood (UCB) for the northern population of Tunisia.Our study included full-term newborns by vaginal deliveries. Hematol
Autor:
Houssem Sellami, Imen Darragi, Samia Mnif, Dorra Chaouachi, Leila Chaouch, Miniar Kalai, Imen Boudrigua, Salem Abbes
Publikováno v:
Journal of pediatric hematology/oncology. 42(1)
OBJECTIVES The 5' upstream region of the HBG1 gene plays a very important role in the expression of fetal hemoglobin (HbF). In contrast, increased HbF levels can inhibit the deoxygenation-induced polymerization of sickle hemoglobin (α2βS2), which l
Autor:
Imen Darragi, Salem Abbes, Imen Boudrigua, Miniar Kalai, Houyem Ouragini, Mouna Ben Sassi, Raouf Hafsia, Leila Chaouch, Imen Moumni, Dorra Chaouachi
Publikováno v:
Acta Haematologica Polonica. 47:242-247
Background and aim Sickle cell anemia (SCA) is characterized by variable patterns of clinical expression. Polymorphisms linked to different genes have been associated with specific complications of the disease. Herein, we focused on the study of the
Autor:
Emna Barkaoui, Imen Boudrigua, Faten Haddad, Nawel Trabelsi, Samia Menif, Salem Abbes, Dorra Chaouachi, Imen Darragi, Leila Chaouch, Mouna Jaouani
Publikováno v:
European Journal of Medical Genetics. 64:104139
Introduction Unconjugated hyperbilirubinemia (UCB) is a feature of Gilbert's syndrome (GS) and Crigler-Najjar's syndrome (CNS), which are two hereditary defects in bilirubin metabolism. Both syndromes are linked to mutations in the UGT1A1 gene, which
Autor:
Imen Moumni, Dorra Chaouachi, Imen Darragi, Marwa Dridi, Fethi Mellouli, Miniar Kalai, Salem Abbes, Mohamed Bejaoui, Leila Chaouch, Imen Boudrigua, Houyem Ouragini
Publikováno v:
Hematology (Amsterdam, Netherlands). 22(3)
Mediators of adhesion become a potential new target for pharmacological therapy to struggle the complications of sickle cell disease (SCD). Several mechanisms for increased adherence have been postulated and the well-studied are CD36 and VLA4 which e
Autor:
Imen Moumni, Leila Chaouch, Imen Boudrigua, Dorra Chaouachi, Miniar Kalai, Houyem Ouragini, Raouf Hafsia, Salem Abbes, Imen Darragi
Publikováno v:
Hematology
Hematology, Maney Publishing, 2016, 21 (7), pp.425-429. ⟨10.1080/10245332.2015.1107275⟩
Hematology, Maney Publishing, 2016, 21 (7), pp.425-429. ⟨10.1080/10245332.2015.1107275⟩
International audience; Aims: Fetal hemoglobin (HbF) modulates the phenotype of sickle cell anemia (SCA) by inhibiting deoxy sickle hemoglobin (HbS) polymerization. HbF genes are genetically regulated, and the level of HbF and its distribution among
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21277295c1491fa73ad821a294d0762a
https://hal-riip.archives-ouvertes.fr/pasteur-01374983
https://hal-riip.archives-ouvertes.fr/pasteur-01374983
Autor:
Leila, Chaouch, Miniar, Kalai1, Imen, Darragi, Imen, Boudrigua, Dorra, Chaouachi, Slim Ben, Ammar, F, Mellouli, M, Bjaoui, Salem, Abbes
Publikováno v:
Hematology (Amsterdam, Netherlands). 21(2)
Hyperbilirubinemia is often observed in chronic hemolysis and results in the formation of pigment cholelithiasis that could be increased by the presence of defected enzymes involved in the bilirubin metabolism. Indeed, this is the first report that i