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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A gain-of-function mutation in zinc cluster transcription factor Rob1 drives Candida albicans adaptive growth in the cystic fibrosis lung environment von Gnaien, Mayssa, Maufrais, Corinne, Rebai, Yasmine, Kallel, Aicha, Ma, Laurence, Hamouda, Samia, Khalsi, Fatma, Meftah, Khaoula, Smaoui, Hanen, Khemiri, Monia, Hadj Fredj, Sondes, Bachellier-Bassi, Sophie, Najjar, Imène, Messaoud, Taieb, Boussetta, Khadija, Kallel, Kalthoum, Mardassi, Helmi, d'Enfert, Christophe, Bougnoux, Marie-Elisabeth, Znaidi, Sadri

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Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6‐10_16delTTTG deletion von Amri, Yessine, Dabboubi, Rym, Mghaieth, Fathia, Zili, Mohamed, Messaoud, Taieb, Casini, Alessandro, De Moerloose, Philippe, Toumi, Nour El Houda

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Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme von Chkioua, Latifa, Amri, Yessine, Chaima, Sahli, Fenni, Ferdawes, Boudabous, Hela, Ben Turkia, Hadhami, Messaoud, Taieb, Tebib, Neji, Laradi, Sandrine

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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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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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Cystic fibrosis in Tunisian children: a review of 32 children von Boussetta, Khedija, Khalsi, Fatma, Bahri, Yasmine, Belhadj, Imen, Tinsa, Faten, Messaoud, Taieb Ben, Hamouda, Samia

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Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme von Chkioua, Latifa, Amri, Yessine, Chaima, Sahli, Fenni, Ferdawes, Boudabous, Hela, Ben Turkia, Hadhami, Messaoud, Taieb, Tebib, Neji, Laradi, Sandrine

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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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Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects von Khemir, Sameh, Halayem, Soumeyya, Azzouz, Hatem, Siala, Hajer, Ferchichi, Maherzia, Guedria, Asma, Bedoui, Amel, Abdelhak, Sonia, Messaoud, Taieb, Tebib, Neji, Belhaj, Ahlem, Kaabachi, Naziha

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Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b von Chkioua, Latifa, Amri, Yessine, Sahli, Chayma, Rhouma, Ferdawes Ben, Chehida, Amel Ben, Tebib, Neji, Messaoud, Taieb, Abdennebi, Hassen Ben, Laradi, Sandrine

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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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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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Molecular Characterization of Mycobacterium tuberculosis Strains Resistant to Isoniazid von Smaoui, S, Siala, M, Hadj Fredj, S, Kammoun, S, Marouane, C, Hachicha, S, Ghorbel, A, Gdoura, R, Slim, L, Ben Messaoud, T, Messadi, F

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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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Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci von Quemener, Sylvia, Chen, Jian-Min, Chuzhanova, Nadia, Bénech, Caroline, Casals, Teresa, Macek Jr, Milan, Bienvenu, Thierry, McDevitt, Trudi, Farrell, Philip M., Loumi, Ourida, Messaoud, Taieb, Cuppens, Harry, Cutting, Garry R., Stenson, Peter D., Giteau, Karine, Audrézet, Marie-Pierre, Cooper, David N., Férec, Claude

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Identification of RS2234253 T96K polymorphism of TREM2 gene in Tunisian Alzheimer's disease population von Fray, Saloua, Achouri, Afef, Jamoussi, Hela, Mahmoud, Mariem Ben, Ali, Nadia Ben, Messaoud, Taieb, Fradj, Mohamed

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Genotypic and Phenotypic Characteristics of Tunisian Isoniazid-Resistant Mycobacterium tuberculosis Strains von Soudani, Alya, Rabta University Hospital, Tunis, Tunisia, Hadjfredj, Sondess, Children Hospital, Tunis, Tunisia, Zribi, Meriem, Rabta University Hospital, Tunis, Tunisia, Messaadi, Feriel, Hedi Chaker Hospital, Sfax, Tunisia, Messaoud, Taieb, Children Hospital, Tunis, Tunisia, Masmoudi, Afef, Rabta University Hospital, Tunis, Tunisia, Zribi, Mohamed, Hedi Chaker Hospital, Sfax, Tunisia, Fendri, Chedlia, Rabta University Hospital, Tunis, Tunisia

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Missing apolipoprotein E ɛ4 allele associated with nonamnestic Alzheimer’s disease in a Tunisian population von Fray, Saloua, Achouri-Rassas, Afef, Belal, Samir, Messaoud, Taieb

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