Characterising a diversity of coastal community fisheries in Kiribati and Vanuatu von Campbell, Brooke, Steenbergen, Dirk, Li, Owen, Sami, Abel, Nikiari, Beia, Delisle, Aurélie, Neihapi, Pita, Uriam, Tarateiti, Andrew, Neil

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Leveraging deep learning and computer vision technologies to enhance management of coastal fisheries in the Pacific region von Shedrawi, George, Magron, Franck, Vigga, Bernard, Bosserelle, Pauline, Gislard, Sebastien, Halford, Andrew R., Tiitii, Sapeti, Fepuleai, Faasulu, Molai, Chris, Rota, Manibua, Jalam, Shivam, Fatongiatau, Viliami, Sami, Abel P., Nikiari, Beia, Sokach, Ada H. M., Joy, Lucy A., Li, Owen, Steenbergen, Dirk J., Andrew, Neil L.

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Coastal fisheries and community-based support systems in post disaster contexts von Obregón, Clara, Sokach, Ada, Neihapi, Pita, Arudere, Ajay, Joy, Lucy, Ephraim, Regina, Ham, Jayven, Koran, Douglas, Malverus, Vasemaca, Sami, Abel, Gereva, Sompert, Steenbergen, Dirk J.

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Sustainability in Mega-Events: Beyond Qatar 2022 von Meza Talavera, Abel, Al-Ghamdi, Sami, Koç, Muammer

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Ethics of performing dermatologic cosmetic enhancement procedures in adolescents von Gitin, Alexander, Samia, Arthur M., Torres, Abel, Grant-Kels, Jane M., Saikaly, Sami K.

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Short-to long-term deformation behavior of glassy polymers under cyclic uniaxial, torsional, and multiaxial loads von Holopainen, Sami, Barriere, Thierry, Gabrion, Xavier, Cherouat, Abel

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Carrier-Phase Recovery for Coherent Optical Systems: Algorithms, Challenges and Solutions von Neves, Manuel S., Lorences-Riesgo, Abel, Martins, Celestino S., Mumtaz, Sami, Charlet, Gabriel, Monteiro, Paulo P., Guiomar, Fernando P.

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Leveraging Dispersion-Aware Phase Recovery for Long-Haul Digital Multi-Carrier Transmission: An Experimental Demonstration von Neves, Manuel S., Lorences-Riesgo, Abel, Martins, Celestino S., Mumtaz, Sami, Frignac, Yann, Charlet, Gabriel, Monteiro, Paulo P., Dris, Stefanos, Guiomar, Fernando P.

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Neonatal Scn1b-null mice have sinoatrial node dysfunction, altered atrial structure, and atrial fibrillation von Ramos-Mondragon, Roberto, Edokobi, Nnamdi, Hodges, Samantha L, Wang, Shuyun, Bouza, Alexandra A, Canugovi, Chandrika, Scheuing, Caroline, Juratli, Lena, Abel, William R, Noujaim, Sami F, Madamanchi, Nageswara R, Runge, Marschall S, Lopez-Santiago, Luis F, Isom, Lori L

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Short- to long-term deformation behavior, failure, and service life of amorphous polymers under cyclic torsional and multiaxial loadings von Barriere, T., Cherouat, A., Gabrion, X., Holopainen, S.

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Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients von Ouederni, Monia, Vincent, Quentin B., Frange, Pierre, Touzot, Fabien, Scerra, Sami, Bejaoui, Mohamed, Bousfiha, Aziz, Levy, Yves, Lisowska-Grospierre, Barbara, Canioni, Danielle, Bruneau, Julie, Debré, Marianne, Blanche, Stéphane, Abel, Laurent, Casanova, Jean-Laurent, Fischer, Alain, Picard, Capucine

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On the Mitigation of WSS Filtering Penalties: Single- vs Multi-Carrier Modulation von Loureiro, Pedro A., Lorences-Riesgo, Abel, Mumtaz, Sami, Neves, Manuel S., Le Gac, Dylan, Nguyen, Trung-Hien, Frignac, Yann, Zhao, Yu, Monteiro, Paulo P., Charlet, Gabriel, Dris, Stefanos, Guiomar, Fernando P.

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Maximizing Fiber Capacity in Flex-Grid Coherent Systems Through Symbol Rate Optimization von Lorences-Riesgo, Abel, Le Gac, Dylan, Sales-Llopis, Marti, Mumtaz, Sami, Martins, Celestino S., de Jauregui Ruiz, Ivan F., Dris, Stefanos, Frignac, Yann, Charlet, Gabriel

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Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia von Alodayani, Abdulrahman N., Al-Otaibi, Abdulnasir M., Deswarte, Caroline, Frayha, Husn Habib, Bouaziz, Matthieu, AlHelale, Maryam, Le Voyer, Tom, Nieto-Patlan, Alejandro, Rattina, Vimel, AlZahrani, Mofareh, Halwani, Rabih, Al Sohime, Fahad, Al-Mousa, Hamoud, Al-Muhsen, Saleh, Alhajjar, Sami H., Dhayhi, Nabil S., Abel, Laurent, Casanova, Jean-Laurent, Bin-Hussain, Ibrahim, AlBarrak, May S., Al-Jumaah, Suliman A., Bustamante, Jacinta

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Inherited IL-12p40 Deficiency: Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds von Prando, Carolina, Samarina, Arina, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Cobat, Aurelie, Picard, Capucine, AlSum, Zobaida, Al-Jumaah, Suliman, Al-Hajjar, Sami, Frayha, Husn, Al-Mousa, Hamoud, Ben-Mustapha, Imen, Adimi, Parisa, Feinberg, Jacqueline, de Suremain, Maylis, Jannière, Lucile, Filipe-Santos, Orchidée, Mansouri, Nahal, Stephan, Jean-Louis, Nallusamy, Revathy, Kumararatne, Dinakantha S., Bloorsaz, Mohamad Reza, Ben-Ali, Meriem, Elloumi-Zghal, Houda, Chemli, Jalel, Bouguila, Jihene, Bejaoui, Mohamed, Alaki, Emadia, AlFawaz, Tariq S., Al Idrissi, Eman, ElGhazali, Gehad, Pollard, Andrew J., Murugasu, Belinda, Wah Lee, Bee, Halwani, Rabih, Al-Zahrani, Mohammed, Al Shehri, Mohammed A., Al-Zahrani, Mofareh, Bin-Hussain, Ibrahim, Mahdaviani, Seyed Alireza, Parvaneh, Nima, Abel, Laurent, Mansouri, Davood, Barbouche, Ridha, Al-Muhsen, Saleh, Casanova, Jean-Laurent

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Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity von Ku, Cheng-Lung, von Bernuth, Horst, Picard, Capucine, Zhang, Shen-Ying, Chang, Huey-Hsuan, Yang, Kun, Chrabieh, Maya, Issekutz, Andrew C, Cunningham, Coleen K, Gallin, John, Holland, Steven M, Roifman, Chaim, Ehl, Stephan, Smart, Joanne, Tang, Mimi, Barrat, Franck J, Levy, Ofer, McDonald, Douglas, Day-Good, Noorbibi K, Miller, Richard, Takada, Hidetoshi, Hara, Toshiro, Al-Hajjar, Sami, Al-Ghonaium, Abdulaziz, Speert, David, Sanlaville, Damien, Li, Xiaoxia, Geissmann, Frédéric, Vivier, Eric, Maródi, László, Garty, Ben-Zion, Chapel, Helen, Rodriguez-Gallego, Carlos, Bossuyt, Xavier, Abel, Laurent, Puel, Anne, Casanova, Jean-Laurent

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A novel form of human STAT1 deficiency impairing early but not late responses to interferons von Kong, Xiao-Fei, Ciancanelli, Michael, Al-Hajjar, Sami, Alsina, Laia, Zumwalt, Timothy, Bustamante, Jacinta, Feinberg, Jacqueline, Audry, Magali, Prando, Carolina, Bryant, Vanessa, Kreins, Alexandra, Bogunovic, Dusan, Halwani, Rabih, Zhang, Xin-Xin, Abel, Laurent, Chaussabel, Damien, Al-Muhsen, Saleh, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie

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Inherited Interleukin-12 Deficiency: IL12B Genotype and Clinical Phenotype of 13 Patients from Six Kindreds von Picard, Capucine, Fieschi, Claire, Altare, Frédéric, Al-Jumaah, Suliman, Al-Hajjar, Sami, Feinberg, Jacqueline, Dupuis, Stéphanie, Soudais, Claire, Al-Mohsen, Ibrahim Zaid, Génin, Emmanuelle, Lammas, David, Kumararatne, Dinakantha S., Leclerc, Tony, Rafii, Arash, Frayha, Husn, Murugasu, Belinda, Wah, Lee Bee, Sinniah, Raja, Loubser, Michael, Okamoto, Emi, Al-Ghonaium, Abdulaziz, Tufenkeji, Haysam, Abel, Laurent, Casanova, Jean-Laurent

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Early diagnosis and successful long-term management of a rare, severe lysosomal acid lipase deficiency/Wolman disease patient: Infancy to age five von Cossette, Antoine, Castilloux, Julie, Bouffard, Chantal, Laflamme, Julie, Faure, Christophe, Benlamlih, Sami, Abel, Florian, Beecroft, Michael, Francis, Mira, Drouin, Regen

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Lopinavir/ritonavir monotherapy versus current treatment continuation for maintenance therapy of HIV-1 infection: the KALESOLO trial von Meynard, Jean-Luc, Bouteloup, Vincent, Landman, Roland, Bonnard, Philippe, Baillat, Vincent, Cabie, André, Kolta, Sami, Izopet, Jacques, Taburet, Anne-Marie, Mercie, Patrick, Chene, Geneviève, Girard, Pierre-Marie

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