Myelodysplastic syndromes and bone loss in mice and men von Weidner, H, Rauner, M, Trautmann, F, Schmitt, J, Balaian, E, Mies, A, Helas, S, Baschant, U, Khandanpour, C, Bornhäuser, M, Hofbauer, L C, Platzbecker, U

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Evolution of NPM1-negative therapy-related myelodysplastic syndromes following curative treatment of NPM1-mutant AML von Herold, S, Sockel, K, Sayehli, C, Herbst, R, Dührsen, U, Oelschlägel, U, Böttner, A, Hindahl, H, Kullmer, J, Helas, S, Sauer, M, Mohr, B, Mies, A, Bornhäuser, M, Ehninger, G, Röllig, C, Thiede, C, Platzbecker, U

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P-259 Therapy-related MDS after curative intensive therapy for de novo acute myeloid leukemia – An emerging clinical entity? von Helas, S, Röllig, C, Dührsen, U, Herbst, R, Schaich, M, Thiede, C, Mohr, B, Kramer, M, Trautmann-Grill, K, Von Bonin, M, Bornhäuser, M, Ehninger, G, Platzbecker, U

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Efficacy of antithrombotic therapy in chronic heart failure: The HELAS study von Cokkinos, Dennis V., Haralabopoulos, George C., Kostis, John B., Toutouzas, Pavlos K.

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Induction of short-term remission with single agent eltrombopag in refractory nucleophosmin-1-mutated acute myeloid leukemia von Platzbecker, Uwe, Sockel, Katja, Schönefeldt, Claudia, Nowak, Daniel, Helas, Susann, Röllig, Christoph, Mossner, Maximilian, Jann, Johann Christoph, Ehninger, Gerhard, Hofmann, Wolf-Karsten, Bornhäuser, Martin, Thiede, Christian, Wermke, Martin

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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, Ben Youssef, Ilhem Turki, 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.

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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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Eruzioni di carta. Quattro secoli di stampa sui vulcani Buch-Ausbrücke. Vulkanisches in historischen Drucken aus vier Jahrhunderten von Monaco, Annachiara, Perrone, Antonio

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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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Inhibition of Receptor Activator of NF-{kappa}B Ligand by Denosumab Attenuates Vascular Calcium Deposition in Mice von Helas, Susann, Goettsch, Claudia, Schoppet, Michael, Zeitz, Ute, Hempel, Ute, Morawietz, Henning, Kostenuik, Paul J, Erben, Reinhold G, Hofbauer, Lorenz C

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Is large for gestational age in singletons born after frozen embryo transfer associated with freezing technique or endometrial preparation protocol? A longitudinal national French... von Hesters, Laetitia, Sermondade, Nathalie, Lambert, Céline, Pouly, Jean-Luc, Pereira, Bruno, Lucas, Cécily, Levy, Rachel, Brugnon, Florence

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Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines von Dreux, Sophie, Rosenblatt, Jonathan, Benachi, Alexandra, Voirin‐Mathieu, Etienne, Muller, Françoise, Boitte, F., Denis, M. C., Lorenter, P., Jouval, M., Sitruk, B., Suybeng, V., Herbreteau, S., Treyssac, F., Gras, V., Guiot, J., Savarit, D., Blouin, P., Zanusso, M., Clément, P., Brossaud, J., Fischer, I., Moineau, M. P., Kerspern, H., Andlauer, P., Gaeremynck, E., Berchiche, S., Barba, F., Lebrun, C., Terrier, N., Kemeny, S., Delevallée, C., Marceau, G., Gehrke, C., Lemaire, S., Ménégaut, L., Lefaure, G., Petit, V., Gauchez‐Quenin, A. S., Pavili, L., Chevallier‐Helas, F., Artur, F., Sigogneau, P., Groussin, H., Renom, G., Lepers, S., Chianéa, T., Veyrat, B., Le Querler, L., Martin‐Denavit, T., Sault, C., Galland, A., Cheillan, D., Brechard, M. P., Yerokine, P., Levy‐Mozziconacci, A., Toga, C., Sainte‐Rose, M., Wasels, R., Aubertin, D., Rahil, H., Roucaute, T., Boulle, N., Solassol, J., Minery, M., Baillet, C., Dauch, P., Chevillon, I., Masson, D., Rotella, C. M., Barguil, Y., Duhin, M., Got, L., Lachgar, M., Druart, L., Ramirez, J. M., Lacroix, I., Brethome, B., Cassuto, G., Cohen‐Bacrie, M., Ternaux, F., Beaujard, M. P., Annette‐Reisch, M., Bounaud, M. P., Nowak, E., Dossot, J. M., Odaert, H., Quillard Murain, M., Descombes, G., Belot, G., Tisseur, B., Gouneaud, J., Louzier, C., Tosetti, F., Romain, S., Handwerk, L., Molignier, R., De Mas, P., Le Van, M., Estepa, B., Tang, K.

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