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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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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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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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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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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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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Role of vitamin D receptor polymorphism in multiple sclerosis disease course von Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ali, Nadia Ben, Messaoud, Taieb, Hannachi, Amal, Fradj, Mohamed

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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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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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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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Vitamin D receptor gene BsmI (rs1544410) polymorphism: role in multiple sclerosis and genotype-phenotype correlations von Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ben Ali, Nadia, Messaoud, Taieb, Hannachi Salhi, Amel, Fredj, Mohamed

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Glucose-6-phosphate dehydrogenase deficiency in Tunisian jaundiced neonates von Dabboubi, Rym, Amri, Yessine, Hamdi, Soumaya, Jouini, Hamida, Sahli, Chaima, Fredj, Sondess Hadj, Salem, Kamel Ben, ElhoudaToumi, Nour, Messaoud, Taieb

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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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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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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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Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease von Achouri-Rassas, Afef, Ali, Nadia Ben, Cherif, Aroua, Fray, Saloua, Siala, Hajer, Zakraoui, Nouria Oudiaa, Hadj-Fredj, Sondes, Kechaou, Mariem, Anane, Nadia, Echebi, Slim, Messaoud, Taieb, Belal, Samir

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Early psychiatrics symptoms in familial Alzheimer’s disease with presenilin 1 mutation (I83T) von Fray, Saloua, Ali, Nadia Ben, Rassas, Afef Achouri, Kechaou, Meriem, Oudiaa, Nouria, Cherif, Aroua, Echebbi, Slim, Messaoud, Taieb, Belal, Samir

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Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease von Achouri-Rassas, Afef, Ben Ali, Nadia, Fray, Saloua, Hadj Fredj, Sondes, Kechaou, Meriem, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Chabbi, Slim, Anane, Nadia, Messaoud, Taieb, Gouider, Riadh, Belal, Samir

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Rapid diagnostic tests : Pros, cons and potential use in the COVID-19 management in Tunisia von Jameleddine Chtioui, Mouna, Grati, Hela, Harzallah, Nabil, Odabachian Jebali, Marie Christine, Trabelsi, Abdelhalim, Ben Ahmed, Mélika, Thabet, Lamia, Mhalla, Salma, Ben Moussa, Mohamed, Messaoud, Taieb, Ben Romdhane, Habiba, Toumi, Adnene, Hamouda, Chokri

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