Epidemiology and disease burden of tuberculosis in south of Tunisia over a 22-year period: Current trends and future projections von Ben Ayed, Houda, Koubaa, Makram, Gargouri, Lamia, Ben Jemaa, Maissa, Trigui, Maroua, Hammemi, Fatma, Ben Hmida, Mariem, Mahfoudh, Abdelmajid, Zalila, Neila, Mustapha, Aida, Masmoudi, Chokri, Marrakchi, Chakib, Yaich, Sourour, Messaadi, Feriel, Ayedi, Ali, Damak, Jamel, Ben Jemaa, Mounir

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Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012) von Mellouli, Fethi, Mustapha, Imen Ben, Khaled, Monia Ben, Besbes, Habib, Ouederni, Monia, Mekki, Najla, Ali, Meriem Ben, Larguèche, Beya, Hachicha, Mongia, Sfar, Tahar, Gueddiche, Neji, Barsaoui, Siheme, Sammoud, Azza, Boussetta, Khadija, Becher, Saida Ben, Meherzi, Ahmed, Guandoura, Najoua, Boughammoura, Lamia, Harbi, Abdelaziz, Amri, Fethi, Bayoudh, Fethi, Jaballah, Najla Ben, Tebib, Neji, Bouaziz, Asma, Mahfoudh, Abdelmajid, Aloulou, Hajer, Mansour, Lamia Ben, Chabchoub, Imen, Boussoffara, Raoudha, Chemli, Jalel, Bouguila, Jihène, Hassayoun, Saida, Hammami, Saber, Habboul, Zakia, Hamzaoui, Agnès, Ammar, Jamel, Barbouche, Mohamed-Ridha, Bejaoui, Mohamed

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A rare case of recurrent laryngeal hamartoma von Hsairi, Manel, Chaabene, Maha, Moalla, imene, Chaabouni, Hela, Hammemi, Bouthayna, Gargouri, Lamia, Charfeddine, Ilhem, Mahfoudh, Abdelmajid

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An unusual case of pediatric acute nicotine poisoning due to a dermal exposure von Weli, Manel, Jerbi, Mouna, Chakroun-Walha, Olfa, Maalej, Bayen, Gargouri, Lamia, Rekik, Noureddine, Mahfoudh, Abdelmajid

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Pediatric Ischemic Stroke Following Scorpion Sting von Weli, Manel, Moalla, Imene, Hsairi, Manel, Trichelli, Sahar, Mahfoudh, Abdelmajid, Maalej, Bayene, Gargouri, Lamia

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Pediatric Ischemic Stroke Following Scorpion Sting: Authors’ Reply von Weli, Manel, Moalla, Imene, Hsairi, Manel, Trichelli, Sahar, Mahfoudh, Abdelmajid, Maalej, Bayene, Gargouri, Lamia

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A Child Surviving Rabies in Tunisia: A Case Report von Asma, Ben Halima, Amal, Elleuch, Hela, Fendri, Khaled, Frikha, Mariem, Handous, Lamia, Gargouri, Abdelmajid, Mahfoudh

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Neurobrucellosis Presenting as Vocal Cord Paralysis in an Infant von Weli, Manel, Moalla, Imene, Feki, Wiem, Moalla, Nour, Hsairi, Manel, Trichelli, Sahar, Mahfoudh, Abdelmajid, Mnif, Zeineb, Maalej, Bayene, Gargouri, Lamia

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Hypertension in Children von Hsairi, Manel, Moalla, Imen, Ammar, Saloua, Sallemi, Sahla, Safi, Faiza, Gargouri, Lamia, Mhiri, Riadh, Mahfoudh, Abdelmajid

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Metabolic Syndrome in the Development of Gallstone Disease in Children von Sahla, Sellami, Saloua, Ammar, Manel, Hsairi, Imen, Moalla, Abdelmajid, Mahfoudh, Mahdi, Bendhaou, Riadh, Mhiri

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Neurobrucellosis Presenting as Vocal Cord Paralysis in an Infant: Authors’ Reply von Weli, Manel, Moalla, Imene, Feki, Wiem, Moalla, Nour, Hsairi, Manel, Trichelli, Sahar, Mahfoudh, Abdelmajid, Mnif, Zeineb, Maalej, Bayene, Gargouri, Lamia

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Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochond... von Alila-Fersi, Olfa, Chamkha, Imen, Majdoub, Imen, Gargouri, Lamia, Mkaouar-Rebai, Emna, Tabebi, Mouna, Tlili, Abdelaziz, Keskes, Leila, Mahfoudh, Abdelmajid, Fakhfakh, Faiza

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Antinuclear antibodies in children: clinical signification and diagnosis utility von Mejdoub, Sabrina, Hachicha, Hend, Gargouri, Lamia, Feki, Sawsan, Mahfoudh, Abdelmajid, Masmoudi, Hatem

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Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss : A whole mitoc... von Alila-Fersi, Olfa, Chamkha, Imen, Majdoub, Imen, Gargouri, Lamia, Mkaouar-Rebai, Emna, Tabebi, Mouna, Tlili, Abdelaziz, Keskes, Leila, Mahfoudh, Abdelmajid, Fakhfakh, Faiza

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Bifocal pulmonary abscess in an infant and successful surgical management von Ammar, Saloua, Fedj, Myriam Ben, Wali, Manel, Mahfoudh, Abdelmajid, Dhaou, Mahdi Ben, Mhiri, Riadh

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Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patients von Jlajla, Hend, Dehman, Fatma, Jallouli, Manel, Khedher, Rania, Ayadi, Imen, Zerzeri, Yosr, Laadhar, Lilia, Sfar, Imen, Mahfoudh, Abdelmajid, Gorgi, Yosr, Cheour, Elhem, Zouaghi, Karim, Gargah, Tahar, Kallel Sellami, Maryam

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Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients von Ouadani, Hanen, Ben-Mustapha, Imen, Ben-ali, Meriem, Ben-khemis, Leila, Larguèche, Beya, Boussoffara, Raoudha, Maalej, Sonia, Fetni, Ilhem, Hassayoun, Saida, Mahfoudh, Abdelmajid, Mellouli, Fethi, Yalaoui, Sadok, Masmoudi, Hatem, Bejaoui, Mohamed, Barbouche, Mohamed-Ridha

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Molecular basis of complement factor I deficiency in T unisian atypical haemolytic and uraemic syndrome patients von Jlajla, Hend, Dehman, Fatma, Jallouli, Manel, Khedher, Rania, Ayadi, Imen, Zerzeri, Yosr, Laadhar, Lilia, Sfar, Imen, Mahfoudh, Abdelmajid, Gorgi, Yosr, Cheour, Elhem, Zouaghi, Karim, Gargah, Tahar, Kallel Sellami, Maryam

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Diagnostic tardif de la neuroborréliose de Lyme et échange plasmatique von Elleuch, Amal, Loukil, Mouna, Hsairi, Manel, Feki, Manel, Gargouri, Lamia, Mahfoudh, Abdelmajid

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Congenital heart disease in 37,294 births in Tunisia: birth prevalence and mortality rate von Abid, Dorra, Elloumi, Anis, Abid, Leila, Mallek, Souad, Aloulou, Hajer, Chabchoub, Imen, Bouraoui, Amira, Thabet, Afef, Gargouri, Lamia, Zribi, Malek, Yaich, Sourour, Hachicha, Mongia, Gargouri, Abdellatif, Mahfoudh, Abdelmajid, Maatoug, Samir, Dammak, Jamel, Kammoun, Samir

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