Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation von Ennouri, Mariem, Zimmer, Andreas D, Bahloul, Emna, Chaabouni, Rim, Marrakchi, Slaheddine, Turki, Hamida, Fakhfakh, Faiza, Bougacha-Elleuch, Noura, Fischer, Judith

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Identification of a novel missense mutation in NIPAL4 gene: First 3D model construction predicted its pathogenicity von Laadhar, Sahar, Ben Mansour, Riadh, Marrakchi, Slaheddine, Miled, Nabil, Ennouri, Mariem, Fischer, Judith, Kaddechi, Mohamed Ali, Turki, Hamida, Fakhfakh, Faiza

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Pustular psoriasis of pregnancy: Clinical and genetic characteristics in a series of eight patients and review of the literature von Ennouri, Mariem, Bahloul, Emna, Sellami, Khadija, Marrakchi, Slaheddine, Fakhfakh, Faiza, Turki, Hamida, Bougacha‐Elleuch, Noura

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Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations von Hotz, Alrun, Fölster-Holst, Regina, Oji, Vinzenz, Bourrat, Emmanuelle, Frank, Jorge, Marrakchi, Slaheddine, Ennouri, Mariem, Wankner, Lotta, Komlosi, Katalin, Alter, Svenja, Fischer, Judith

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Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying IABCA12/I Mutations von Hotz, Alrun, Fölster-Holst, Regina, Oji, Vinzenz, Bourrat, Emmanuelle, Frank, Jorge, Marrakchi, Slaheddine, Ennouri, Mariem, Wankner, Lotta, Komlosi, Katalin, Alter, Svenja, Fischer, Judith

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Pustular Psoriasis of Pregnancy: Clinical and Genetic Characteristics in a Series of 8 Patients and Review of the Literature von Mariem, Ennouri, Emna, Bahloul, Khadija, Sellami, Slaheddine, Marrakchi, Faiza, Fakhfakh, Hamida, Turki, Noura, Bougacha-Elleuch

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Epidemiological characteristics, management, and outcomes of atrial fibrillation in TUNISIA: Results from the National Tunisian Registry of Atrial Fibrillation (NATURE‐AF) von Ouali, Sana, Ben Halima, Afef, Chabrak, Sonia, Chettaoui, Rafik, Ben Halima, Manel, Haggui, Abdeddayem, Krichane, Salma, Noureddine, Larbi, Marrakchi, Sonia, Charfeddine, Selma, Hassine, Majed, Sayahi, Khaled, Abbes Mohamed, Fehmi, Nasraoui, Wided, Ajmi, Hassen, Ben Miled, Mehdi, Jebbari, Zeynab, Meghaieth, Mohamed Ali, Allouche, Emna, Mechmeche, Rachid, Zakhama, Lilia, Sdiri, Wissem, Ben Khalfallah, Ali, Gharbi, Anissa, Milouchi, Sami, Neji, Ali, Antit, Saoussen, Battikh, Kais, Drissa, Meriem, Kaabachi, Samira, Najar, Tarek, Tlili, Rami, Chahbani, Iheb, Charfeddine, Hanene, Ben, Mbarek Mohamed, Braham, Sami, Maatouk, Faouzi, Abdesselem, Salem, Ayari, Mokdad, Garbaa, Riadh, Hamrouni, Nabil, Mbarek, Dorra, Rekik, Hajer, Zaghdoudi, Hamda, Ayadi, Wacef, Baraket, Feriel, Ben Brahim, Karim, Ben Romdhane, Mariem, Bousadia, Habib, Brahim, Wassim, Mezri, Malek, Guesmi, Ali, Ounissi, Taha, Kammoun, Sofiene, Smati, Wajih, Tlili, Samir, Zoughi, Karim, Zemni, Jawher, Cheikh Bouhlel, Mahmoud, Islem, Sanaa, Jemli, Rym, Joulak, Anissa, Mzoughi, Khadija, Naanea, Hela, Hached, Leila, Hadrich, Moufid, Hmem, Mohamed, Kacem, Slim, Kammoun, Ikram, Othmani, Rawdha, Ouerghi, Amel, Abid, Syrine, Ennouri, Ridha, Haidar, Sandrine, Heraiech, Sihem, Jammali, Monia, Jarrar, Mourad, Riahi, Leila, Trimech, Basma, Azaiez, Med Ali, Azzouzi, Foued, Ben Jemaa, Khaled, Ben Rejab, Oussema, Chrigui, Rim, Wechtati, Wejdene, Boughzela, Essia, Jridi, Gouider, Bezdah, Leila, Kraiem, Sondes, Drissa, Habiba, Ben Youssef, Soraya, Fehri, Wafa, Kachboura, Salem, Gamra, Habib, Kammoun, Samir, Mourali, Mohamed Sami, Addad, Faouzi, Abid, Leila

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Long-term clinical follow-up and molecular testing for diagnosis of the first Tunisian family with Alström syndrome von Chakroun, Amine, Ben Said, Mariem, Ennouri, Amine, Achour, Imen, Mnif, Mouna, Abid, Mohamed, Ghorbel, Abdelmonem, Marshall, Jan D, Naggert, Jürgen K, Masmoudi, Saber

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