Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA1c quantification von Doggui, Radhouene, Abdelhafidh Sahli, Chaïma, Aissa, Wassef Lotfi, Hammami, Maroua, Ben Sedrine, Maha, Mahjoub, Rahma, Zouaoui, Khemais, Daboubi, Rim, Siala, Hajer, Messaoud, Taieb, Bibi, Amina

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Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA 1c quantification von Doggui, Radhouene, Abdelhafidh Sahli, Chaïma, Aissa, Wassef Lotfi, Hammami, Maroua, Ben Sedrine, Maha, Mahjoub, Rahma, Zouaoui, Khemais, Daboubi, Rim, Siala, Hajer, Messaoud, Taieb, Bibi, Amina

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Detection of a novel splicing mutation causing analbuminemia in a Libyan family von Bibi, Amina, Jouini, Latifa, Sahli, Chaima Abdelhafidh, Hadj Fredj, Sondess, Abidi, Kamel, Gharsallah, Lamia, Mathlouthi, Sondess, Ouali, Faida, Siala, Hajer, Belhaj, Raja, Sammoud, Azza, Messaoud, Taieb

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δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tu... von Sahli, Chaima Abdelhafidh, Bibi, Amina, Ouali, Faida, Siala, Hajer, Fredj, Sondess Hadj, Othmani, Rym, Ouenniche, Fekria, Cheour, Mondher, Fitouri, Zohra, Becher, Saida Ben, Messaoud, Taieb

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Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population von Laouini, Naouel, Sahli, Chaima Abdelhafidh, Jouini, Latifa, Haloui, Sabrine, Fredj, Sondes Hadj, Daboubi, Rym, Siala, Hajer, Ouali, Faida, Becher, Meriam, Toumi, Nourelhouda, Bibi, Amina, Messsaoud, Taieb

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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 von 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

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Setup of a Protocol of Molecular Diagnosis of [beta]-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC) von 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

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Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC) von 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

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Fortuitous description of haemoglobin A2' [δ16 (A13) Gly→Arg (GGC→CGC)] in a Tunisian family: study of the molecular defect and its origin von Sahli, Chaima Abdelhafidh, Gritli, Sami, Dabboubi, Rym, Omar, Souheil, Siala, Hajer, Kaabachi, Naziha, Bibi, Amina, Messaoud, Taieb

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Molecular identification of Gd A- and Gd B- G6PD deficient variants by ARMS-PCR in a Tunisian population von Haloui, Sabrine, Laouini, Naouel, Sahli, Chaima Abdelhafidh, Daboubi, Rim, Becher, Mariem, Jouini, Latifa, Kazdaghli, Kalthoum, Tinsa, Faten, Cherif, Semia, Khemiri, Monia, Fredj, Sondess Hadj, Othmani, Rim, Ouali, Faida, Siala, Hajer, Toumi, Nour El Houda, Barsaoui, Sihem, Bibi, Amina, Messaoud, Taieb

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A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del von Dabboubi, Rym, Amri, Yessine, Yahyaoui, Salem, Mahjoub, Rahma, Sahli, Chayma Abdelhafidh, Sahli, Chaima, Hadj Fredj, Sondess, Bibi, Amina, Sammoud, Azza, Messaoud, Taieb

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