Compound blue nevus: A misleading pigmented melanocytic tumor von Baklouti, Massara, Sellami, Khadija, Elleuch, Neila, Rekik, Mariem, Saguem, Ines, Kamoun, Chahir, Gouiaa, Naourez, Ben Messaoud, Hela, Karray, Fathi, Abdelmoula, Mohamed, Sellami, Tahia, Turki, Hamida

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Compound blue nevus: A misleading pigmented melanocytic tumor von Baklouti, Massara, Sellami, Khadija, Elleuch, Neila, Rekik, Mariem, Saguem, Ines, Kamoun, Chahir, Gouiaa, Naourez, Ben Messaoud, Hela, Karray, Fathi, Abdelmoula, Mohamed, Sellami, Tahia, Turki, Hamida

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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 von 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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Orbital pacing of the early Eocene source rock deposition in Tunisia (Bou Dabbous Formation): Astrobiochronological insights into cyclicities through surface-subsurface integration von Messaoud, Jihede Haj, Ben Jemai, Hela Fakhfakh, Yaich, Chokri

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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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The Eocene‐Oligocene Transition in the South‐Western Neo‐Tethys (Tunisia): Astronomical Calibration and Paleoenvironmental Changes von Messaoud, Jihede Haj, Thibault, Nicolas, Yaich, Chokri, Monkenbusch, Johannes, Omar, Hamdi, Jemai, Hela Fakhfakh Ben, Watkins, David K.

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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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Self-Reported Anxiety, Depression and Coping in Parents of Children with Phenylketonuria von Abdelaziz, Rim Ben, Chehida, Amel Ben, Chakchouk, Henda Kachouri, Messaoud, Sana Ben, Hajji, Hela, Boudabous, Hela, Ferchichi, Maherzia, Azzouz, Hatem, Tebib, Néji

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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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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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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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High Frequency of Cardiovascular Complications in Tunisian Kawasaki Disease Patients: Need for a Further Awareness von Ben Chehida, Amel, Ben Messaoud, Sana, Ben Abdelaziz, Rim, Boudabous, Hela, Oujra, Mariem, Ben Turkia, Hadhami, Abdelmoula, Mohamed Slim, Azzouz, Hatem, Hakim, Kaothar, Tebib, Neji

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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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Role play for genetic counseling learning: Value and students perceptions von Ben Abdelaziz, Rim, Boudabous, Hela, Hajji, Hela, Ben Messaoud, Sana, Azzouz, Hatem, Ben Chehida, Amel, Tebib, Neji

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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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Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner–Hanhart Syndrome von Bouyacoub, Yosra, Zribi, Hela, Azzouz, Hatem, Nasrallah, Fehmi, Abdelaziz, Rim Ben, Kacem, Monia, Rekaya, Ben, Messaoud, Olfa, Romdhane, Lilia, Charfeddine, Cherine, Bouziri, Mustapha, Bouziri, Sonia, Tebib, Neji, Mokni, Mourad, Kaabachi, Naziha, Boubaker, Samir, Abdelhak, Sonia

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Étude de l’association de la maladie d’Alzheimer au polymorphisme rs118104841(T>C) de l’intron 14 du gène microtubule associated protein Tau (MAPT) au sein d’une population tunisie... von Fray, Saloua, Achouri-Rassas, Afef, Ben Ali, Nadia, Jamoussi, Hela, Aroua, Cherif, Messaoud, Taieb, Mohamed, Fradj

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Obsessive–compulsive disorder: a new risk factor for Alzheimer disease? von Mrabet Khiari, Hela, Achouri, Afef, Ben Ali, Nadia, Cherif, Aroua, Batti, Hend, Messaoud, Taieb, Mrabet, Amel

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High APOE epsilon 4 allele frequencies associated with Alzheimer disease in a Tunisian population von Rassas, Afef Achouri, Mrabet Khiari, Hela, Hadj Fredj, Sondes, Sahnoun, Safa, Batti, Hend, Zakraoui, Nouria Oudiaa, Cherif, Aroua, Anane, Nadia, Ben Ali, Nadia, Messaoud, Taieb, Mrabet, Amel

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A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype–genotype correlation von REKAYA, MARIEM BEN, MESSAOUD, OLFA, MEBAZAA, AMEL, RIAHI, OLFA, AZAIEZ, HELA, KEFI, RIM, ZGHAL, MOHAMED, BOUBAKER, SAMIR, AMOURI, AHLEM, OSMAN-DHAHRI, AMEL BEN, ABDELHAK, SONIA, MOKNI, MOURAD

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