The Role of Toll-Like Receptors in Skin Host Defense, Psoriasis, and Atopic Dermatitis von Sun, Lixiang, Zhang, Ling-juan, Liu, Wenjie

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Single Nucleotide Polymorphisms in TLR4 Affect Susceptibility to Tuberculosis in Mexican Population from the State of Veracruz von Licona-Limón, Ileana, Sánchez-Hernández, Beatriz, Hernández-Bazán, Sujhey, Ortega, Enrique, Fuentes-Dominguez, Javier

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Genetic Polymorphisms of Toll-like receptors 2 and 9 as Susceptibility Factors for the Development of Ankylosing Spondylitis and Psoriatic Arthritis von Visentainer, Jeane Eliete Laguila, Sell, Ana M., Quirino, Marília G., Rocha-Loures, Marco A., Macedo, Luciana C., Neves, Janisleya S. F., Martinez, Gabriela F., Moraes, A. G., Oliveira-Toré, Camila F., Alves, Hugo Vicentin

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Advances in Acoustics and Vibration: Proceedings of the International Conference on Acoustics and Vibration (ICAV2016), March 21-23, Hammamet, Tunisia von Fakhfakh, Tahar, Chaari, Fakher, Walha, Lasaad, Abdennadher, Moez, Abbes, Mohamed Slim, Haddar, Mohamed

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Modeling and Simulation for Electric Vehicle Applications

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Advances in Acoustics and Vibration II: Proceedings of the Second International Conference on Acoustics and Vibration (ICAV2018), March 19-21, 2018, Hammamet, Tunisia von Fakhfakh, Tahar, Karra, Chafik, Bouaziz, Slim, Chaari, Fakher, Haddar, Mohamed

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Mucinous cystadenoma of the kidney von Charfi, S, Ayadi, L, Khabir, A, Gouiaa, N, Fakhfakh, I, Bahri, I, Makni, S, Boudawara, T S

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ILAE Genetics Literacy series: Progressive myoclonus epilepsies von Cameron, Jillian M, Ellis, Colin A, Berkovic, Samuel F

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Carcinome mucineux primitif cutané von Gouiaa, N., Abbes, K., Khabir, A., Kallel, R., Fakhfakh, I., Bahri, I., Ayadi, L., Meziou, T.J., Makni, S., Boudawara-Sellami, T.

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ILAE genetic literacy series: Focal cortical dysplasia von Macdonald-Laurs, Emma, Leventer, Richard J

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Dirofilariose cutanée von Bahri Zouari, I., Samet Fakhfakh, I., Gouiaa, N., Chtourou, I., Ayadi, L., Kallel, R., Khabir, A., Makni, F., Sellami Boudawara, T.

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Unusual thyroid lesion von Abbes, K, Khabir, A, Chtourou, I, Fakhfakh, I Samet, Gouiaa, N, Bahri, I, Dhouib, H, Ghorbel, A, Boudawara, T Sellami

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Genome Tunisia Project: paving the way for precision medicine in North Africa von Hamdi, Yosr, Trabelsi, Mediha, Ghedira, Kais, Boujemaa, Maroua, Ben Ayed, Ikhlas, Charfeddine, Cherine, Souissi, Amal, Rejeb, Imen, Kammoun Rebai, Wafa, Hkimi, Chaima, Neifar, Fadoua, Jandoubi, Nouha, Mkaouar, Rahma, Chaouch, Melek, Bennour, Ayda, Kamoun, Selim, Chaker Masmoudi, Hend, Abid, Nabil, Mezghani Khemakhem, Maha, Masmoudi, Saber, Saad, Ali, BenJemaa, Lamia, BenKahla, Alia, Boubaker, Samir, Mrad, Ridha, Kamoun, Hassen, Abdelhak, Sonia, Gribaa, Moez, Belguith, Neila, Kharrat, Najla, Hmida, Dorra, Rebai, Ahmed

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Oxalosis and necrotizing pulmonary aspergillosis: About two cases von Chtourou, I, Zouari, I Bahri, Gouiaa, N, Fakhfakh, I, Charfi, S, Kacem, A Hadj, Boudawara, T Sellami

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Characterization of the Mechanical and Vibration Behavior of Flax Composites with an Interleaved Natural Viscoelastic Layer von Hajer, Daoud, Abderrahim, El Mahi, Jean-Luc, Rebiere, Mohamed, Taktak, Mohamed, Haddar

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A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene von Fendri-Kriaa, Nourhene, Hsairi, Ines, Kifagi, Chamseddine, Ellouze, Emna, Mkaouar-Rebai, Emna, Triki, Chahnez, Fakhfakh, Faiza

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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria von Jellouli, Nadege Kammoun, Hadj Salem, Ikhlass, Ellouz, Emna, Kamoun, Zeineb, kamoun, Fatma, tlili, Abdelaziz, Kaabachi, Naziha, Triki, Chanez, Fakhfakh, Faiza

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Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease von Kammoun Jellouli, Nadege, Hadj Salem, Ikhlass, Ellouz, Emna, Louhichi, Nacim, tlili, Abdelaziz, Kammoun, Fatma, Triki, Chanez, Fakhfakh, Faiza

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Identification of a new Arylsulfatase A ( ARSA ) gene mutation in Tunisian patients with metachromatic leukodystrophy (MLD) von Dorboz, Imen, Eymard-Pierre, Eleonore, Kefi, Rym, Abdelhak, Sonia, Miladi, Najoua, Boespflug-Tanguy, Odile

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Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in Tunisia von Talmoudi, Faten, Kammoun, Lobna, Benhalim, Nizar, Torjemane, Lamia, Ouederni, Monia, Aissaoui, Lamia, Lakhal, Amel, Mellouli, Fethi, Othmen, Tarek B, Bejaoui, Mohamed, Abdelhak, Sonia, Meddeb, Mounira, Dellagi, Koussay, Hdiji, Sondes, Amouri, Ahlem

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