Search Results - "Dakhlaoui, Boutheina"

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia by Sahli, Chaima Abdelhafidh, Bibi, Amina, Ouali, Faida, Fredj, Sondess Hadj, Dakhlaoui, Boutheina, Othmani, Rym, Laouini, Naouel, Jouini, Latifa, Ouenniche, Fekria, Siala, Hajer, Touhami, Imed, Becher, Mariem, Fattoum, Slaheddine, Toumi, Nour El Houda, Messaoud, Taieb

“…In Tunisia, thalassemia and sickle cell disease represent the most prevalent monogenic hemoglobin disorders with 2.21% and 1.89% of carriers, respectively…”
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Setup of a Protocol of Molecular Diagnosis of [beta]-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC) by Sahli, Chaima Abdelhafidh, Ben Salem, Ikbel, Jouini, Latifa, Laouini, Naouel, Dabboubi, Rym, Hadj Fredj, Sondes, Siala, Hajer, Othmeni, Rym, Dakhlaoui, Boutheina, Fattoum, Slaheddine, Bibi, Amina, Messaoud, Taieb

“…Backgrounds [beta]-Thalassemia is one of the most prevalent worldwide autosomal recessive disorders. It presents a great molecular heterogeneity resulting from…”
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Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC) by Sahli, Chaima Abdelhafidh, Ben Salem, Ikbel, Jouini, Latifa, Laouini, Naouel, Dabboubi, Rym, Hadj Fredj, Sondes, Siala, Hajer, Othmeni, Rym, Dakhlaoui, Boutheina, Fattoum, Slaheddine, Bibi, Amina, Messaoud, Taieb

“…Backgrounds β‐Thalassemia is one of the most prevalent worldwide autosomal recessive disorders. It presents a great molecular heterogeneity resulting from more…”
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Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia by Sahli, Chaima A, Bibi, Amina, Ouali, Faida, Fredj, Sondess Hadj, Dakhlaoui, Boutheina, Othmani, Rym, Laaouini, Naouel, Jouini, Latifa, Ouenniche, Fekria, Siala, Hajer, Touhami, Imed, Becher, Mariem, Fattoum, Slaheddine, El Houda Toumi, Nour, Messaoud, Taieb

“…In Tunisia, thalassemia and sickle cell disease (SS) represent the most prevalent monogenic hemoglobin disorders with 2.21% and 1.89% of carriers,…”
Get more information