Sjögren's syndrome in association with Crohn's disease by Kaaniche, Fatma Medhioub, Allela, Rania, Frikha, Imen, Charfeddine, Amel

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Sister Mary Joseph's nodule: report of five cases by Masmoudi, Abderrahmen, Boudaya, Sonia, Charfeddine, Amel, Dammak, Anis, Amouri, Mariem, Khabir, Abdelmajid, Marrekchi, Sleheddine, Bouassida, Samir, Sallemi, Tahia, Krichen, Mohamed Salah, Turki, Hamida, Zahaf, Abdelmajid

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Cutaneous metastasis of Crohn's disease by Masmoudi, Abderrahmen, Abdelmaksoud, Wafa, Bouassida, Samir, Khabir, Abdelmajid, Charfeddine, Amel, Fourati, Hela, Boudawara, Tahia, Baklouti, Sofiane, Krichen, Mohamed, Turki, Hamida, Zahaf, Abdelmajid

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Sjögren's syndrome in association with Crohn's disease by Kaaniche, Fatma Medhioub, Allela, Rania, Frikha, Imen, Charfeddine, Amel

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Localisations cutanées métastatiques d’une maladie de Crohn by Masmoudi, Abderrahmen, Abdelmaksoud, Wafa, Bouassida, Samir, Khabir, Abdelmajid, Charfeddine, Amel, Fourati, Hela, Boudawara, Tahia, Baklouti, Sofiane, Krichen, Mohamed, Turki, Hamida, Zahaf, Abdelmajid

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Sister Mary Joseph's nodule: report of five cases by Masmoudi, Abderrahmen, Boudaya, Sonia, Charfeddine, Amel, Dammak, Anis, Amouri, Mariem, Khabir, Abdelmajid, Marrekchi, Sleheddine, Bouassida, Samir, Sallemi, Tahia, Krichen, Mohamed Salah, Turki, Hamida, Zahaf, Abdelmajid

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The morbid cutaneous anatomy of the human genome revealed by a bioinformatic approach by Romdhane, Lilia, Bouhamed, Heni, Ghedira, Kais, Ben Hamda, Cherif, Louhichi, Amel, Jmel, Haifa, Romdhane, Safa, Charfeddine, Chérine, Mokni, Mourad, Abdelhak, Sonia, Rebai, Ahmed

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SSR marker-assisted screening of commercial tomato genotypes under salt stress by Gharsallah, Charfeddine, Abdelkrim, Ahmed Ben, Fakhfakh, Hatem, Salhi-Hannachi, Amel, Gorsane, Faten

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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment by Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Turki Ben Youssef, Ilhem, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha

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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health by Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hajer, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health by Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hager, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

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Epidemiologic features and management of hypertension in Tunisia, the results from the Hypertension National Registry (NaTuRe HTN) by Abid, Leila, Hammami, Rania, Chamtouri, Ikram, Drissa, Meriam, Boudiche, Selim, Bahloul, MohamedAmine, BenSlima, Hedi, Sayahi, Khaled, Charfeddine, Selma, Allouche, Emna, Rais, Lamia, Kaab, Badr, IbnHadjamor, Hassen, BenFatma, Lilia, Garbaa, Riadh, Boukhris, Sabrine, Halima, Manel Ben, Amdouni, Nesrine, Ghorbel, Chaima, Soudani, Sabrine, Khaled, Imen, Triki, Syrine, Bouazizi, Feten, Jemai, Imen, Abdeljalil, Ouday, Ammar, Yemna, Farah, Amani, Neji, Adnen, Oumayma, Zeineb, Seghaier, Sana, Mokrani, Samir, Thawaba, Hamza, Sarray, Hela, Ouaghlani, Khalil, Thabet, Houssem, Mnif, Zeineb, Boujelban, Fatma, Sghaier, Mohamed, Khalifa, Roueida, Fourati, Sami, Kammoun, Yasmin, Abid, Syrine, Hamza, Chihab, Jeddou, Syrine Ben, Sabbah, Lassaad, Lakhdhar, Rim, Dammak, Najla, Sellami, Tarek, Herbegue, Basma, Koubaa, Alia, Triki, Faten, Ellouz, Tarek, Hmoudi, Aicha, BenAmeur, Ikhlas, Boukhchina, MohamedMongi, Abid, Neila, Wachtati, Wejdene, Nasrallah, Nizar, Houidi, Yousra, Meghaieth, Fathia, Ghodhbane, Elhem, Chayeb, Mounira, Chenik, Sarra, Kaabachi, Samira, Saadaoui, Nizar, BenAmeur, Ines, Affes, Moufida, Ouali, Sana, Chaker, Mouna, Naanaa, Hela, Dghim, Meriem, Jarrar, Mourad, Mnif, Jihene, Turki, Ahmed, Zairi, Ihsen, Langar, Jamel, Dardouri, Safa, Hchaichi, Imen, Chettaoui, Rafik, Essmat, Wajih, Chakroun, Amel, Mzoughi, Khadija, Mechmeche, Rachid, BenHalima, Afef, BenKhala, Sahar, Chtourou, Slim, Maalej, Abdelkader, Ayari, Mohsen, Hadrich, Moufid, Tlili, Rami, Azaiez, Fares, Bouhlel, Imen, Sahnoun, Samira, Jerbi, Habib, BenMrad, Imtinene, Riahi, Leila, Sahnoun, Mohamed, BenJemaa, Abdelhamid, BenSalem, Amel, Rekik, Bassem

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Clinical, histological and genetic investigation of Buschke–Fischer–Brauer's disease in Tunisian families by Bchetnia, Mbarka, Charfeddine, Cherine, Kassar, Selma, Hanchi, Imen, Tounsi-Guettiti, Haifa, Rebai, Ahmed, Osman, Amel Dhahri-Ben, Kubisch, Christian, Abdelhak, Sonia, Boubaker, Samir, Mokni, Mourad

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Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports by Bchetnia, Mbarka, Merdassi, Ahlem, Charfeddine, Cherine, Mgaieth, Fatma, Kassar, Selma, Ouechtati, Farah, Chouchene, Ibtissem, Boussen, Hamouda, Mokni, Mourad, Osman, Amel Dhahri-Ben, Boubaker, Med Samir, Abdelhak, Sonia, Elmatri, Leila

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Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis by Ouragini, Houyem, Cherif, Faïka, Daoud, Wafa, Kassar, Selma, Charfeddine, Chérine, Rebaï, Ahmed, Boubaker, Samir, Ben Osman-Dhahri, Amel, Abdelhak, Sonia

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Immunohistological study of involucrin expression in Darier's disease skin by Kassar, Selma, Charfeddine, Cherine, Zribi, Hela, Tounsi-Kettiti, Haifa, Bchetnia, Mbarka, Jerbi, Emna, Cassio, Doris, Mokni, Mourad, Abdelhak, Sonia, Ben Osman, Amel, Boubaker, Samir

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