Profound differences in IgE and IgG recognition of micro‐arrayed allergens in hyper‐IgE syndromes von Garib, Victoria, Ben‐Ali, Meriem, Kundi, Michael, Curin, Mirela, Yaakoubi, Roukaya, Ben‐Mustapha, Imen, Mekki, Najla, Froeschl, Renate, Perkmann, Thomas, Valenta, Rudolf, Barbouche, Mohamed‐Ridha

Volltext

Correction to: The Seven STAT3‑Related Hyper‑IgE Syndromes von Fadil, Ilham, Ben‑Ali, Meriem, Jeddane, Leila, Barbouche, Mohamed‑Ridha, Bousfiha, Ahmed Aziz

Volltext

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988–2012) von Mellouli, Fethi, Mustapha, Imen Ben, Khaled, Monia Ben, Besbes, Habib, Ouederni, Monia, Mekki, Najla, Ali, Meriem Ben, Larguèche, Beya, Hachicha, Mongia, Sfar, Tahar, Gueddiche, Neji, Barsaoui, Siheme, Sammoud, Azza, Boussetta, Khadija, Becher, Saida Ben, Meherzi, Ahmed, Guandoura, Najoua, Boughammoura, Lamia, Harbi, Abdelaziz, Amri, Fethi, Bayoudh, Fethi, Jaballah, Najla Ben, Tebib, Neji, Bouaziz, Asma, Mahfoudh, Abdelmajid, Aloulou, Hajer, Mansour, Lamia Ben, Chabchoub, Imen, Boussoffara, Raoudha, Chemli, Jalel, Bouguila, Jihène, Hassayoun, Saida, Hammami, Saber, Habboul, Zakia, Hamzaoui, Agnès, Ammar, Jamel, Barbouche, Mohamed-Ridha, Bejaoui, Mohamed

Volltext

Failure analysis of a stainless steel component operating inside an acid leaching reactor von ElJersifi, Adnane, Ben Ali, Meriem, El Maalam, Khadija, Chbihi, Abdelouahed, Aouadi, Khalil, Ouzaouit, Khalid, Naamane, Sanae

Volltext

Evolutionary dynamics of human Toll-like receptors and their different contributions to host defense von Barreiro, Luis B, Ben-Ali, Meriem, Quach, Hélène, Laval, Guillaume, Patin, Etienne, Pickrell, Joseph K, Bouchier, Christiane, Tichit, Magali, Neyrolles, Olivier, Gicquel, Brigitte, Kidd, Judith R, Kidd, Kenneth K, Alcaïs, Alexandre, Ragimbeau, Josiane, Pellegrini, Sandra, Abel, Laurent, Casanova, Jean-Laurent, Quintana-Murci, Lluís

Volltext

Homozygous transcription factor 3 gene (TCF3) mutation is associated with severe hypogammaglobulinemia and B-cell acute lymphoblastic leukemia von Ben-Ali, Meriem, PhD, Yang, Jing, MD, Chan, Koon Wing, MPhil, Ben-Mustapha, Imen, MD, Mekki, Najla, MD, Benabdesselem, Chaouki, PhD, Mellouli, Fethi, MD, Bejaoui, Mohamed, MD, Yang, Wanling, PhD, Aissaoui, Lamia, MD, Lau, Yu Lung, MD, Barbouche, Mohamed-Ridha, MD, PhD

Volltext

Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population von Barbouche, Mohamed-Ridha, Mekki, Najla, Ben-Ali, Meriem, Ben-Mustapha, Imen

Volltext

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes von Yaakoubi, Roukaya, Mekki, Najla, Ben-Mustapha, Imen, Ben-Khemis, Leila, Bouaziz, Asma, Ben Fraj, Ilhem, Ammar, Jamel, Hamzaoui, Agnès, Turki, Hamida, Boussofara, Lobna, Denguezli, Mohamed, Haddad, Samir, Ouederni, Monia, Bejaoui, Mohamed, Chan, Koon Wing, Lau, Yu Lung, Mellouli, Fethi, Barbouche, Mohamed-Ridha, Ben-Ali, Meriem

Volltext

Autoimmune lymphoproliferative syndrome caused by homozygous FAS mutations with normal or residual protein expression von Agrebi, Nourhen, PhD, Mansour, Lamia Ben, MD, Medhaffar, Moez, MD, Hadiji, Sondes, MD, Fedhila, Faten, MD, Ben-Ali, Meriem, MD, Mekki, Najla, MD, Hachicha, Mongia, MD, Barsaoui, Sihem, MD, Barbouche, Mohamed-Ridha, MD, PhD, Ben-Mustapha, Imen, MD

Volltext

Toll-Like Receptor 2 Arg677Trp Polymorphism Is Associated with Susceptibility to Tuberculosis in Tunisian Patients von Ben-Ali, Meriem, Barbouche, Mohamed-Ridha, Bousnina, Soufia, Chabbou, Abdellatif, Dellagi, Koussay

Volltext

Relationship between toll-like receptor 2 nonsynonymous single nucleotide polymorphisms and the effectiveness of Bacille Calmette-Guérin immunotherapy in preventing recurrence of s... von Ajili, Faouzia, PhD, Boubaker, Samir, MD, Derouiche, Amine, MD, Ali, Meriem Ben, PhD, Mustapha, Imen Ben, MD, Cherif, Mohamed, MD, Chebil, Mohamed, MD, Mannai, Mohamed, PhD, Barbouche, Mohamed-Ridha, MD, PhD

Volltext

Functional characterization of naturally occurring genetic variants in the human TLR1-2-6 gene family von Ben-Ali, Meriem, Corre, Beatrice, Manry, Jérémy, Barreiro, Luis B., Quach, Hélène, Boniotto, Michele, Pellegrini, Sandra, Quintana-Murci, Lluís

Volltext

Study of human RIG-I polymorphisms identifies two variants with an opposite impact on the antiviral immune response von Pothlichet, Julien, Burtey, Anne, Kubarenko, Andriy V, Caignard, Gregory, Solhonne, Brigitte, Tangy, Frédéric, Ben-Ali, Meriem, Quintana-Murci, Lluis, Heinzmann, Andrea, Chiche, Jean-Daniel, Vidalain, Pierre-Olivier, Weber, Alexander N R, Chignard, Michel, Si-Tahar, Mustapha

Volltext

Peering into recent advances in passivation strategies of few-layer black phosphorene toward battery anodes: A review von Mansouri, Zouhir, Yaden, Afaf, El Manjli, Faissal, Ben Ali, Meriem, Tiouitchi, Ghassane, Naamane, Sanae, Mounkachi, Omar, El Maalam, Khadija

Volltext

The Effect of Heat Treatments on the Properties of a Ferritic High-Chromium Cast Iron von ElJersifi, Adnane, Aouadi, Khalil, Ben Ali, Meriem, Chbihi, Abdelouahed, Semlal, Nawal, Bouaouine, Hassan, Naamane, Sanae

Volltext

Defective glycosylation leads to defective gp130-dependent STAT3 signaling in PGM3-deficient patients von Ben-Ali, Meriem, Ben-Khemis, Leila, Mekki, Najla, Yaakoubi, Roukaya, Ouni, Rym, Benabdessalem, Chaouki, Ben-Mustapha, Imen, Barbouche, Mohamed-Ridha

Volltext

Regulatory T-cell dysfunction and cutaneous exposure to Staphylococcus aureus underlie eczema in DOCK8 deficiency von Wilkie, Hazel, Das, Mrinmoy, Pelovitz, Tyler, Bainter, Wayne, Woods, Brian, Alasharee, Mohammed, Sobh, Ali, Baris, Safa, Eltan, Sevgi Bilgic, Al-Herz, Waleed, Barbouche, Mohamed-Ridha, Ben-Mustapha, Imen, Ben-Ali, Meriem, Sallam, Mohamed T.H., Awad, Amany, Lotfy, Sohilla, El Marsafy, Aisha, Ezzelarab, Moushira, Farrar, Michael, Schmidt, Brigitta A.R., NandyMazumdar, Monali, Guttman-Yassky, Emma, Sheets, Anthony, Vidic, Katie Maria, Murphy, George, Schlievert, Patrick M., Chou, Janet, Leyva-Castillo, Juan Manuel, Janssen, Erin, Timilshina, Maheshwor, Geha, Raif S.

Volltext

The Seven STAT3-Related Hyper-IgE Syndromes von Fadil, Ilham, Ben-Ali, Meriem, Jeddane, Leila, Barbouche, Mohamed-Ridha, Bousfiha, Ahmed Aziz

Volltext

Hypomorphic homozygous mutations in phosphoglucomutase 3 ( PGM3 ) impair immunity and increase serum IgE levels von Sassi, Atfa, PhD, Lazaroski, Sandra, PhD, Wu, Gang, MSc, Haslam, Stuart M., PhD, Fliegauf, Manfred, PhD, Mellouli, Fethi, MD, Patiroglu, Turkan, MD, Unal, Ekrem, MD, Ozdemir, Mehmet Akif, MD, Jouhadi, Zineb, MD, Khadir, Khadija, MD, Ben-Khemis, Leila, MSc, Ben-Ali, Meriem, PhD, Ben-Mustapha, Imen, MD, Borchani, Lamia, PhD, Pfeifer, Dietmar, PhD, Jakob, Thilo, MD, Khemiri, Monia, MD, Asplund, A. Charlotta, BSc, Gustafsson, Manuela O., MSc, Lundin, Karin E., PhD, Falk-Sörqvist, Elin, MSc, Moens, Lotte N., PhD, Gungor, Hatice Eke, MD, Engelhardt, Karin R., PhD, Dziadzio, Magdalena, MD, PhD, Stauss, Hans, MD, PhD, Fleckenstein, Bernhard, MD, Meier, Rebecca, BSc, Prayitno, Khairunnadiya, MSc, Maul-Pavicic, Andrea, PhD, Schaffer, Sandra, Rakhmanov, Mirzokhid, PhD, Henneke, Philipp, MD, Kraus, Helene, MSc, Eibel, Hermann, PhD, Kölsch, Uwe, MD, Nadifi, Sellama, PhD, Nilsson, Mats, PhD, Bejaoui, Mohamed, MD, Schäffer, Alejandro A., PhD, Smith, C.I. Edvard, MD, PhD, Dell, Anne, PhD, Barbouche, Mohamed-Ridha, MD, PhD, Grimbacher, Bodo, MD

Volltext

A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients von Ben-Khemis, Leila, Mekki, Najla, Ben-Mustapha, Imen, Rouault, Karen, Mellouli, Fethi, Khemiri, Monia, Bejaoui, Mohamed, Essaddam, Leila, Ben-Becher, Saayda, Boughamoura, Lamia, Hassayoun, Saida, Ben-Ali, Meriem, Barbouche, Mohamed-Ridha

Volltext