Up‐to‐date incidence and initial characteristics of cystic fibrosis in Tunisia von Hamouda, Samia, Hadj Fredj, Sondess, Messaoud, Taieb, Scotet, Virginie, Boussetta, Khadija, Munck, Anne

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Vitamin D status and VDR gene polymorphisms in patients with growth hormone deficiency: A case control Tunisian study von Tombari, Sarra, Amri, Yessine, Hasni, Yosra, Hadj Fredj, Sondess, Salem, Yesmine, Ferchichi, Salima, Essaddam, Leila, Messaoud, Taieb, Dabboubi, Rym

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Clopidogrel utilization in patients with coronary artery disease and diabetes mellitus: should we determine CYP2C192 genotype? von Chouchene, Saoussen, Dabboubi, Rym, Raddaoui, Haythem, Abroug, Hela, Ben Hamda, Khaldoun, Hadj Fredj, Sondess, Abderrazak, Fatma, Gaaloul, Mayssa, Rezek, Marwa, Neffeti, Fadoua, Hellara, Ilhem, Sassi, Mouna, Khefacha, Linda, Sriha, Asma, Nouira, Semir, Najjar, Mohamed Fadhel, Maatouk, Faouzi, Messaoud, Taieb, Hassine, Mohsen

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Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients von Mahmoud, Taher, Sahli, Chaima, Hadj Fredj, Sondess, Amri, Yessine, Othmani, Rim, Mohamed, Ghaber S., Zein, Ekhtelbenina, Messaoud, Taieb

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Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches von Amri, Yessine, Dabboubi, Rym, Khemiri, Monia, Jebabli, Elham, Hadj Fredj, Sondess, Ahmed, Sarra Ben, Jouini, Yosr, Ouali, Faida, Messaoud, Taieb

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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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Epidemiological and clinical characteristics of 66 Tunisian Sickle cell syndrome patients von Sahli, Ahlem, Ouali, Faida, Dabboubi, Rym, Fredj, Sondess Hadj, Meddeb, Nabila, Mzoughi, Naila, 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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Inherited bisalbuminemia with growth hormone deficiency von Dabboubi, Rym, Amri, Yessine, Sahli, Chaima, Fredj, Sondess Hadj, Essaddam, Leila, Zoghlami, Ala, Ben Becher, Saida, Messaoud, Taieb

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Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families von Amri, Yessine, El Houda Toumi, Nour, Fredj, Sondess Hadj, de Moerloose, Philippe

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Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations von Kasmi, Chaima, Amri, Yessine, Hadj-Fredj, Sondess, Oueslati, Sabrine, Dabboussi, Malek, Mahjoub, Rahma, Hammami, Sana, Aljane, Imen, Mami, Faika Ben, Jamoussi, Henda, Messaoud, Taieb, Bibi, Amina

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Association of M470V polymorphism of CFTR gene with variability of clinical expression of asthma: Case-report study von Wahabi, Imen, Hadj Fredj, Sondess, Nefzi, Malek, Dabboubi, Rym, Siala, Hajer, Khalsi, Fatma, Bousetta, Khedija, Messaoud, Taieb

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Preliminary national report on cystic fibrosis epidemiology in Tunisia: the actual state of affairs von Hamouda, Samia, Fredj, Sondess Hadj, Hilioui, Sonia, Khalsi, Fatma, Ameur, Salma Ben, Bouguila, Jihene, Boussoffara, Raoudha, Besbes, Habib, Ajmi, Houda, Mattoussi, Nadia, Messaoud, Taieb, Mehrezi, Ahmed, Hachicha, Mongia, Boughamoura, Lamia, Sfar, Mohamed Taher, Gueddiche, Neji, Abroug, Saoussen, Becheur, Saida Ben, Barsaoui, Sihem, Tebib, Neji, Samoud, Azza, Gandoura, Najoua, Tinsa, Faten, Boussetta, Khadija

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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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Autosomal dominant polycystic kidney disease: identification of two polymorphisms von Sahnoun, Safa, Barbouch, Samia, Hadj Fredj, Sondess, Khedher, Adel, Messaoud, Taieb

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Angiotensin-converting enzyme insertion/deletion gene polymorphism in cystic fibrosis patients von OUESLATI, SABRINE, FREDJ, SONDESS HADJ, SIALA, HAJER, BIBI, AMINA, ALOULOU, HAJER, BOUGHAMOURA, LAMIA, BOUSSETTA, KHADIJA, BARSAOUI, SIHEM, MESSAOUD, 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 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

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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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Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults von Jouini, Latifa, Bibi, Amina, Ouali, Faida, Hadj Fredj, Sondess, Ouennich, Fekria, Siala, Hajer, Messaoud, Taieb, Fattoum, Slaheddine

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New frameshift CF mutation 3729delAinsTCT in a Tunisian cystic fibrosis patient von FREDJ, SONDESS HADJ, BOUDAYA, MONIA, OUESLATI, SABRINE, SAHNOUN, SAFA, SAHLI, CHAIMA, SIALA, HAJER, BOUSSETTA, KHEDIJA, BIBI, AMINA, MESSAOUD, TAIEB

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