Search Results - "Hafsia, Raouf"

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients by Chaouch, Leila, Kalai, Miniar, Jbara, Manel Ben, Chaabene, Arij Ben, Darragi, Imen, Chaouachi, Dorra, Mallouli, Fethi, Hafsia, Raouf, Ghanem, Abderraouf, Abbes, Salem

“…The skeletal manifestations of sickle cell disease are the result of changes in bone and bone marrow caused by chronic tissue hypoxia that is exacerbated by…”
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Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients by Chaouch, Leila, Kalai, Miniar, Chaouachi, Dorra, Mallouli, Fethi, Hafsia, Raouf, Ben Ammar, Slim, Abbes, Salem

“…As a result of chronic hemolysis, hyperbilirubinemia is often observed, leading to the formation of pigment cholelithiasis which could be busted by the…”
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TREATMENT OF ACUTE PROMYELOCYTIC LEUKEMIA WITH AIDA BASED REGIMEN by Jeddi, Ramzi, Ghédira, Hèla, Ben Amor, Ramzi, Ben Abdennebi, Yosr, Karima, Kacem, Mohamed, Zarrouk, Ben Neji, Hend, Aissaoui, Lamia, Ben Lakhal, Raihane, Ben Salah, Naouel, Menif, Samia, Belhadjali, Zaher, Ben Abid, Hela, Gouider, Emna, Hafsia, Raouf, Saad, Ali, Fenaux, Pierre, Meddeb, Balkis

“…In Tunisia, the ATRA era began in 1998 with the use, consecutively, of two regimens combining ATRA and an anthracycline with cytarabine (APL93), and without…”
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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients by Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Kalai, Miniar, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

“…Fetal hemoglobin (HbF) modulates the phenotype of sickle cell anemia (SCA) by inhibiting deoxy sickle hemoglobin (HbS) polymerization. HbF genes are…”
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Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia by Benmansour, Ikbel, Moradkhani, Kamran, Moumni, Imen, Wajcman, Henri, Hafsia, Raouf, Ghanem, Abderraouf, Abbès, Salem, Préhu, Claude

“…We screened 423 patients referred to our laboratory after hemolysis triggered by fava beans ingestion, neonatal jaundice or drug hemolysis. Others were…”
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First description of the rs45496295 polymorphism of the C/EBPE gene in β-thalassemia intermedia patients by Mejri, Awatef, Mansri, Marwa, Hadj Fredj, Sondess, Ouali, Faida, Bibi, Amina, Hafsia, Raouf, Messaoud, Taieb, Siala, Hajer

“…The C/EBPE gene, located in 14q11.2, encodes for a B/zip-type transcription factor. The C/EBPɛ is involved in terminal differentiation and functional maturity…”
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Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome by Haddad, Faten, Trabelsi, Nawel, Chaouch, Leila, Darragi, Imen, Oueslati, Meriem, Boudriga, Imen, Chaouachi, Dorra, El-Borgi, Wijdene, Hafsia, Raouf, Abbes, Salem, Ouragini, Houyem

“…We report here the clinical, hematological and molecular data in a 50-year-old patient with β-thalassemia intermedia (β-TI) caused by a homozygous β + mutation…”
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C0219 Inherited factor XI deficiency: A report of 11 cases and review of literature by Elborgi, Wijdene, Ben Lakhal, Fatma, Ben Salah, Naouel, Zahra, Kaouther, Zorguan, Moez, Meddeb, Balkis, Hafsia, Raouf, Gouider, Emna

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C0200 Clinical and biological features of Von Willebrand disease type 3: Report of a Tunisian series by Ben Lakhal, Fatma, El Borgi, Wijdene, Ben Salah, Naouel, Zahra, Kaouther, Zorguan, Moez, Meddeb, Balkis, Hafsia, Raouf, Gouider, Emna

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C0220 Incidence of hemophilia in the North of Tunisia by Elborgi, Wijdene, Ben Lakhal, Fatma, Ben Salah, Naouel, Zahra, Kaouther, Zorguan, Moez, Meddeb, Balkis, Hafsia, Raouf, Gouider, Emna

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C0197 Evaluation of bleeding symptoms in case of inherited FVII deficiency: About 9 cases by Ben Lakhal, Fatma, El Borgi, Wijdene, Ben Salah, Naouel, Zahra, Kaouther, Meddeb, Balkis, Hafsia, Raouf, Gouider, Emna

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C0204 Factor XIII deficiency: A family report by Ben Lakhal, Fatma, El Borgi, Wijdene, Ben Salah, Naouel, Zahra, Kaouther, Zorguan, Moez, Mahmoudi, Hajer, Meddeb, Balkis, Hafsia, Raouf, Gouider, Emna

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Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients by Ben Sassi, Mouna, Chaouch, Leila, Kalai, Miniar, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

“…Sickle cell anemia (SCA) is characterized by variable patterns of clinical expression. Polymorphisms linked to different genes have been associated with…”
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Immunophenotyping of B chronic lymphoproliferative syndromes (CLL excluded): confrontation with the histology by El Borgi, Wijden, Ben Salah, Nawel, Ben Lakhal, Fatma, Makni, Lamia, Gouider, Emna, Hafsia, Raouf

“…Immunophenotyping is a major tool for the diagnosis of the chronic lymphoïd leukaemia (CLL). Its interest remains limited in the classification of the other B…”
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Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency by Abdallah, Hejer Elmahmoudi, Gouider, Emna, Stambouli, Nejla, Amor, Mohamed Ben, Jlizi, Asma, Belhedi, Nejla, Sassi, Rim, Khodjetelkhil, Houssein, Meddeb, Balkis, Hafsia, Raouf, Hamza, Adel, Elgaaied, Amel Benammar

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Immunophenotyping in adult acute myeloid leukemia: which prognostic value? by Ben Salah, Naouel, Gouider, Emna, Aounallah Skhiri, Hajer, El Borgi, Wijdene, Jouabli, Moenes, Ben Lakhal, Fatma, Jeddi, Ramzi, Hafsia, Raouf

“…Immunophenotyping is an essential step in the diagnosis of acute myeloid leukemia. Its prognostic value remains controversial with contradictory results. To…”
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Iron overload in sickle cell anemia : a study of 94 patients by Hafsia, Raouf, Belakhal, Fatma, Ben Salah, Naouel, Gouider, Emna, Elborgi, Wijden

“…Sickle cell disease is an autosomal, recessive hemoglobinopathy characterized by hemolytic anemia. Red blood cell transfusions are uncommon therapeutic…”
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Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia by Kalai, M, Chaouch, L, Mansour, I B, Hafsia, R, Ghanem, A, Abbes, S

“…The pro-inflammatory context of sickle cell disease promotes the liberation of cytokines such as CCL5, encoded by a gene located on chromosome 17. Herein, the…”
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Evolution of a refractory cytopenia with multilineage dysplasia and ring sideroblasts to chronic myelomonocytic leukemia by Ben Salah, Naouel, Gouider, Emna, Belakhal, Fatma, El Borgi, Wijdene, Menif, Samia, Ben Abid, Hela, Jeddi, Ramzi, Hafsia, Raouf

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Treatment of acute promyelocytic leukemia with PETHEMA LPA 99 protocol: a Tunisian single center experience by Jeddi, Ramzi, Ghédira, Héla, Menif, Samia, Ben Neji, Hend, Ben Amor, Ramzi, Kacem, Karima, Aissaoui, Lamia, Bouteraâ, Walid, Abdennebi, Yosr, Raihane, Ben Lakhal, Gouider, Emna, Raouf, Hafsia, Hèla, Ben Abid, Saad, Ali, Zaher, Belhadjali, Meddeb, Balkis

“…Acute promyelocytic leukemia (APL) has now become the most curable of all subtypes of acute myeloid leukemia. A cure rate of 75-80% can be anticipated with a…”
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