Not logged in.png)
Share.png)
SaveShare Save Prevalence and risk factors of diabetes mellitus and hypertension in North East Tunisia calling for efficient and effective actions
Kheriji, Nadia; Dakhlaoui, Thouraya; Rebai, Wafa Kamoun; Maatoug, Sonia; Thabet, Mohamed Taher; Mellah, Thouraya; Mrad, Mehdi; Trabelsi, Hajer; Soltani, Manel; Kabbage, Maria; Ben Hassine, Hichem; Bahlous, Afef Hadj Salah; Mahjoub, Faten; Jamoussi, Henda; Abid, Abdelmajid; Abdelhak, Sonia; Kefi, Rym Share Save Share Save Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatmentHechmi, Meriem; Charif, Majida; Kraoua, Ichraf; Fassatoui, Meriem; Dallali, Hamza; Desquiret-Dumas, Valerie; Bris, Celine; Goudenege, David; Drissi, Cyrine; Galai, Said; Ouerhani, Slah; Procaccio, Vincent; Amati-Bonneau, Patrizia; Abdelhak, Sonia; Ben Youssef-Turki, Ilhem; Lenaers, Guy; Kefi, Rym Share Save Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanomaChikhaoui, Asma; Jones, Meriem; Rezen, Tadeja; Ben Ahmed, Melika; Naouali, Chokri; Komel, Radovan; Zghal, Mohamed; Boubaker, Samir; Abdelhak, Sonia; Yacoub-Youssef, Houda Share Save Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutationsChikhaoui, Asma; Kraoua, Ichraf; Calmels, Nadege; Bouchoucha, Sami; Obringer, Cathy; Zayoud, Khouloud; Montagne, Benjamin; M'rad, Ridha; Abdelhak, Sonia; Laugel, Vincent; Ricchetti, Miria; Turki, Ilhem; Yacoub-Youssef, Houda Share Save Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case-control study in the Tunisian population and a meta-analysisDallali, Hamza; Hechmi, Meriem; Morjane, Imane; Elouej, Sahar; Jmel, Haifa; Ben Halima, Yosra; Abid, Abdelmajid; Bahlous, Afef; Barakat, Abdelhamid; Jamoussi, Henda; Abdelhak, Sonia; Kefi, Rym Share Save Share Save Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related CancersHamdi, Yosr; Mighri, Najah; Boujemaa, Maroua; Mejri, Nesrine; Ben Nasr, Sonia; Ben Rekaya, Mariem; Messaoud, Olfa; Bouaziz, Hanen; Berrazega, Yosra; Rachdi, Haifa; Jaidane, Olfa; Daoud, Nouha; Zribi, Aref; Ayari, Jihene; El Benna, Houda; Labidi, Soumaya; Ben Hassouna, Jamel; Haddaoui, Abderazzek; Rahal, Khaled; Benna, Farouk; Mrad, Ridha; Ben Ahmed, Slim; Boussen, Hamouda; Boubaker, Samir; Abdelhak, Sonia Share Save Distribution of HCV Genotypes Among People Who Inject Drugs in Tunisia: New Evidence for Scaling Up Prevention and Treatment Toward National Elimination GoalChouikha, Anissa; Ghrabi, Amine; Ghodbane, Amira; Hammemi, Walid; Khedhiri, Marwa; Sadraoui, Amel; Touzi, Henda; Ben Hassine, Hichem; Maatoug, Sonia; Bensaoud, Chaima; Abdelhak, Sonia; Bouarrouj, Samir; Gdoura, Mariem; Chaouachi, Hedia; Triki, Henda Share Save Share Save Share Save The morbid cutaneous anatomy of the human genome revealed by a bioinformatic approachRomdhane, Lilia; Bouhamed, Heni; Ghedira, Kais; Ben Hamda, Cherif; Louhichi, Amel; Jmel, Haifa; Romdhane, Safa; Charfeddine, Cherine; Mokni, Mourad; Abdelhak, Sonia; Rebai, Ahmed Share Save Share Save Share Save ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairsDiStefano, Marina T.; Hemphill, Sarah E.; Oza, Andrea M.; Siegert, Rebecca K.; Grant, Andrew R.; Hughes, Madeline Y.; Cushman, Brandon J.; Azaiez, Hela; Booth, Kevin T.; Chapin, Alex; Duzkale, Hatice; Matsunaga, Tatsuo; Shen, Jun; Zhang, Wenying; Kenna, Margaret; Schimmenti, Lisa A.; Tekin, Mustafa; Rehm, Heidi L.; Abou Tayoun, Ahmad N.; Amr, Sami S.; Abdelhak, Sonia; Alexander, John; Avraham, Karen; Bhatia, Neha; Bai, Donglin; Boczek, Nicole; Brownstein, Zippora; Burt, Rachel; Bylstra, Yasmin; del Castillo, Ignacio; Choi, Byung Yoon; Downie, Lilian; Friedman, Thomas; Giersch, Anne; Goh, Jasmine; Greinwald, John; Griffith, Andrew J.; Hernandez, Amy; Holt, Jeffrey; Hosoya, Makoto; Ying, Lim Jiin; Jain, Kanika; Kim, Un-Kyung; Kremer, Hannie; Krantz, Ian; Leal, Suzanne; Lewis, Morag; Liu, Xue Zhong; Low, Wendy; Lu, Yu; Luo, Minjie; Masmoudi, Saber; Ming, Tan Yuen; Moreno-Pelayo, Miguel Angel; Morin, Matias; Morton, Cynthia; Murray, Jaclyn; Mutai, Hideki; Nara, Kiyomitsu; Pandya, Arti; Pei-Rong, Sylvia Kam; Smith, Richard J. H.; Jamuar, Saumya Shekhar; Suer, Funda Elif; Usami, Shin-Ichi; Van Camp, Guy; Yamazawa, Kazuki; Yuan, Hui-Jun; Black-Zeigelbein, Elizabeth; Zhang, Keijan Share Save Share Save Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twinsJaballah-Gabteni, Amira; Tounsi, Haifa; Kabbage, Maria; Hamdi, Yosr; Elouej, Sahar; Ben Ayed, Ines; Medhioub, Mouna; Mahmoudi, Moufida; Dallali, Hamza; Yaiche, Hamza; Ben Jemii, Nadia; Maaloul, Afifa; Mezghani, Najla; Abdelhak, Sonia; Hamzaoui, Lamine; Azzouz, Mousaddak; Boubaker, Samir Share Save Gut microbiota imbalances in Tunisian participants with type 1 and type 2 diabetes mellitusFassatoui, Meriem; Lopez-Siles, Mireia; Diaz-Rizzolo, Diana A.; Jmel, Haifa; Naouali, Chokri; Abdessalem, Ghaith; Chikhaoui, Asma; Nadal, Belen; Jamoussi, Henda; Abid, Abdelmajid; Gomis, Ramon; Abdelhak, Sonia; Martinez-Medina, Margarita; Kefi, Rym Share Save 
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}