Bacillomycin D and its combination with amphotericin B: promising antifungal compounds with powerful antibiofilm activity and wound‐healing potency von Tabbene, O, Azaiez, S, Di Grazia, A, Karkouch, I, Ben Slimene, I, Elkahoui, S, Alfeddy, M.N, Casciaro, B, Luca, V, Limam, F, Mangoni, M.L

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In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear von Chiereghin, Chiara, Robusto, Michela, Lewis, Morag A, Caetano, Susana, Massa, Valentina, Castorina, Pierangela, Ambrosetti, Umberto, Steel, Karen P, Duga, Stefano, Asselta, Rosanna, Soldà, Giulia

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Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss von Lei, Peiliang, Zhu, Qingwen, Dong, Wenrong, Zhang, Siqi, Sun, Yanyan, Du, Xitong, Geng, Meng, Jiang, Yuan

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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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Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis—Like Autosomal Recessive Congenital... von Charfeddine, Cherine, Laroussi, Nadia, Mkaouar, Rahma, Jouini, Raja, Khayat, Olfa, Redissi, Aladin, Mosbah, Amor, Dallali, Hamza, Chedly Debbiche, Achraf, Zaouak, Anissa, Fenniche, Sami, Abdelhak, Sonia, Hammami-Ghorbel, Houda

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Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan von Kausar, Nabila, Haque, Asma, Masoud, Muhammad Shareef, Nahid, Nazia, Ashfaq, Usman Ali, Waryah, Ali Muhammad, Bhatti, Rashid, Qasim, Muhammad

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SIRT3 promotes auditory function in young adult FVB/nJ mice but is dispensable for hearing recovery after noise exposure von Patel, Sally, Shah, Lisa, Dang, Natalie, Tan, Xiaodong, Almudevar, Anthony, White, Patricia M, Azaiez, Hela

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Deaf intermarriage has limited effect on the prevalence of recessive deafness and no effect on underlying allelic frequency von Braun, Derek C, Jain, Samir, Epstein, Eric, Greenwald, Brian H, Herold, Brienna, Gray, Margaret

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Paraoxonase 3 gene polymorphisms are associated with occupational noise-induced deafness: A matched case-control study from China von Zhou, Huaping, Zhou, Jinpeng, Li, Hui, Hui, Changye, Bi, Jing

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A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia von Romanov, Georgii P, Pshennikova, Vera G, Lashin, Sergey A, Solovyev, Aisen V, Teryutin, Fedor M, Cherdonova, Aleksandra M, Borisova, Tuyara V, Sazonov, Nikolay N, Khusnutdinova, Elza K, Posukh, Olga L, Fedorova, Sardana A, Barashkov, Nikolay A

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Hernie de la graisse orbitaire post COVID 19 von Htira, Y., Azaiez, S.

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Tricellular Tight Junctions in the Inner Ear von Kitajiri, Shin-ichiro, Katsuno, Tatsuya

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Distinct Expression Pattern of a Deafness Gene, KIAA1199, in a Primate Cochlea von Ogawa, Kaoru, Okano, Hideyuki, Fujioka, Masato, Hosoya, Makoto

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Highly porous biochars from different biomasses as potential adsorbents for chromium removal: optimization by response surface methodology von Azaiez, S., Ben Khalifa, E., Magnacca, G., Cesano, F., Bracco, P., Hamrouni, B.

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Nuclear physics for cultural heritage von Kutschera, Walter

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Synthesis and characterization of promising biochars for hexavalent chromium removal: application of response surface methodology approach von Khalifa, E. Ben, Azaiez, S., Magnacca, G., Cesano, F., Benzi, P., Hamrouni, B.

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Hernie de la graisse orbitaire post COVID 19 von Htira, Y., Azaiez, S.

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Prévalence de l’hypogonadisme au cours de l’insuffisance rénale chronique von Oueslati, I, Ounissi, M, Azaiez, S, Belagha, J, Khiari, K, Abdallah, N. Ben, Abdallah, T. Ben

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Prévalence et facteurs de risque de la dysfonction érectile chez les insuffisants rénaux chroniques von Oueslati, I., Ounissi, M., Azaiez, S., Talbi, E., Belagha, J., Khiari, K.

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Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel von Shen, Jun, Oza, Andrea M., del Castillo, Ignacio, Duzkale, Hatice, Matsunaga, Tatsuo, Pandya, Arti, Kang, Hyunseok P., Mar-Heyming, Rebecca, Guha, Saurav, Moyer, Krista, Lo, Christine, Kenna, Margaret, Alexander, John J., Zhang, Yan, Hirsch, Yoel, Luo, Minjie, Cao, Ye, Wai Choy, Kwong, Cheng, Yen-Fu, Avraham, Karen B., Hu, Xinhua, Garrido, Gema, Moreno-Pelayo, Miguel A., Greinwald, John, Zhang, Kejian, Zeng, Yukun, Brownstein, Zippora, Basel-Salmon, Lina, Davidov, Bella, Frydman, Moshe, Weiden, Tzvi, Nagan, Narasimhan, Willis, Alecia, Hemphill, Sarah E., Grant, Andrew R., Siegert, Rebecca K., DiStefano, Marina T., Amr, Sami S., Rehm, Heidi L., Abou Tayoun, Ahmad N.

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