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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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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Agressive small cell neuroendocrine carcinoma of the neck: A case report von Kharrat, G., Ferchichi, S., Azaiez, A., Ferjani, M., Chalbi, E., Marrakchi, J.

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Nuclear physics for cultural heritage von Kutschera, Walter

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Prognostic value of hyperglycemia on-admission in diabetic versus non-diabetic patients presenting with ST-elevation myocardial infarction in Tunisia von Jomaa, Walid, El Mhamdi, Sana, Ben Ali, Imen, Azaiez, Mohamed A., El Hraiech, Aymen, Ben Hamda, Khaldoun, Maatouk, Faouzi

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Risk profile and in-hospital prognosis in elderly patients presenting for acute ST-elevation myocardial infarction in the Tunisian context von Jomaa, Walid, Hamdi, Sonia, Ben Ali, Imen, Azaiez, Mohamed A, El Hraiech, Aymen, Ben Hamda, Khaldoun, Maatouk, Faouzi

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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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Prevalence and prognostic significance of anemia in patients presenting for ST-elevation myocardial infarction in a Tunisian center von Jomaa, Walid, Ben Ali, Imen, Hamdi, Sonia, Azaiez, Mohamed A., Hraïech, Aymen El, Ben Hamda, Khaldoun, Maatouk, Faouzi

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Clinical features and prognosis of infective endocarditis in children: Insights from a Tunisian multicentre registry von Jomaa, Walid, Ben Ali, Imen, Abid, Dorra, Hajri Ernez, Samia, Abid, Leila, Triki, Faten, Kammoun, Samir, Gharbi, Anissa, Ben Rejeb, Oussama, Mahdhaoui, Abdallah, Jeridi, Gouider, Azaiez, Mohamed A, El Hraiech, Aymen, Ben Hamda, Khaldoun, Maatouk, Faouzi

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The Topology of GB-Metric Spaces von Dehghan Nezhad, Akbar, Aral, Zohreh

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Transcriptome Profiling in Hybrid Poplar Following Interactions with Melampsora Rust Fungi von Azaiez, Aïda, Boyle, Brian, Levée, Valérie, Séguin, Armand

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