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收藏A cross-domain test battery for comprehensive hearing loss characterisation using functional, physiological, and vestibular measures跨域测试电池,用于通过功能、生理和前庭测量全面表征听力损失
Buhl, Mareike; Koifman, Shiran; Magbonde, Abile Serge; Kocoglu, Koray; Hochmuth, Sabine; Partouche, Elie; Coez, Arnaud; Radeloff, Andreas; Thai-Van, Hung; Wiener-Vacher, Sylvette; Gerenton, Gregory; Warzybok, Anna; Avan, Paul; Kollmeier, Birger
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收藏Deciphering Auditory Hyperexcitability in Otogl Mutant Mice Unravels an Auditory Neuropathy Mechanism揭示Otogl突变小鼠听觉超兴奋性,阐明了听觉神经病变机制
Gagliardini, M; Mechaussier, S; Pina, CC; Morais, M; Postal, O; Jean, P; Dupont, T; Singh-Estivalet, A; Udugampolage, S; Scandola, C; Verpy, E; Libé-Philippot, B; Inbar, TC; Schwenkgrub, J; Spinola, CMB; Etournay, R; El-Amraoui, A; Bathellier, B; Mallet, A; Delmaghani, S; Giraudet, F; Petit, C; Gourévitch, B; Avan, P; Michalski, N
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收藏Non-invasive intracranial pressure monitoring for high-grade gliomas patients treated with radiotherapy: results of the GMaPIC trial
Casile, Melanie; Thivat, Emilie; Giraudet, Fabrice; Ginzac, Angeline; Molnar, Ioana; Biau, Julian; Brehant, Julien; Lourenco, Blandine; Avan, Paul; Durando, Xavier
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收藏NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice
Chachlaki, Konstantina; Messina, Andrea; Delli, Virginia; Leysen, Valerie; Maurnyi, Csilla; Huber, Chieko; Ternier, Gaetan; Skrapits, Katalin; Papadakis, Georgios; Shruti, Sonal; Kapanidou, Maria; Cheng, Xu; Acierno, James; Rademaker, Jesse; Rasika, Sowmyalakshmi; Quinton, Richard; Niedziela, Marek; L'Allemand, Dagmar; Pignatelli, Duarte; Dirlewander, Mirjam; Lang-Muritano, Mariarosaria; Kempf, Patrick; Catteau-Jonard, Sophie; Niederlaender, Nicolas J.; Ciofi, Philippe; Tena-Sempere, Manuel; Garthwaite, John; Storme, Laurent; Avan, Paul; Hrabovszky, Erik; Carleton, Alan; Santoni, Federico; Giacobini, Paolo; Pitteloud, Nelly; Prevot, Vincent
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收藏Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis导致早发性耳聋显性形式的基因的超早期杂合致病变异是严重的老年性耳聋的基础
Boucher, Sophie; Tai, Fabienne Wong Jun; Delmaghani, Sedigheh; Lelli, Andrea; Singh-Estivalet, Amrit; Dupont, Typhaine; Niasme-Grare, Magali; Michel, Vincent; Wolff, Nicolas; Bahloul, Amel; Bouyacoub, Yosra; Bouccara, Didier; Fraysse, Bernard; Deguine, Olivier; Collet, Lionel; Thai-Van, Hung; Ionescu, Eugen; Kemeny, Jean-Louis; Giraudet, Fabrice; Lavieille, Jean-Pierre; Deveze, Arnaud; Roudevitch-Pujol, Anne-Laure; Vincent, Christophe; Renard, Christian; Franco-Vidal, Valerie; Thibult-Apt, Claire; Darrouzet, Vincent; Bizaguet, Eric; Coez, Arnaud; Aschard, Hugues; Michalski, Nicolas; Lefevre, Gaelle M.; Aubois, Anne; Avan, Paul; Bonnet, Crystel; Petit, Christine
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收藏Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model双AAV介导的基因治疗在DFNB9小鼠模型中恢复听力
Akil, Omar; Dyka, Frank; Calvet, Charlotte; Emptoz, Alice; Lahlou, Ghizlene; Nouaille, Sylvie; de Monvel, Jacques Boutet; Hardelin, Jean-Pierre; Hauswirth, William W.; Avan, Paul; Petit, Christine; Safieddine, Saaid; Lustig, Lawrence R.
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收藏Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome
Dulon, Didier; Papal, Samantha; Patni, Pranav; Cortese, Matteo; Vincent, Philippe F. Y.; Tertrais, Margot; Emptoz, Alice; Tlili, Abdelaziz; Bouleau, Yohan; Michel, Vincent; Delmaghani, Sedigheh; Aghaie, Alain; Pepermans, Elise; Alegria-Prevot, Olinda; Akil, Omar; Lustig, Lawrence; Avan, Paul; Safieddine, Saaid; Petit, Christine; El-Amraoui, Aziz
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收藏CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival
Michel, Vincent; Booth, Kevin T.; Patni, Pranav; Cortese, Matteo; Azaiez, Hela; Bahloul, Amel; Kahrizi, Kimia; Labbe, Menelik; Emptoz, Alice; Lelli, Andrea; Degardin, Julie; Dupont, Typhaine; Aghaie, Asadollah; Oficjalska-Pham, Danuta; Picaud, Serge; Najmabadi, Hossein; Smith, Richard J.; Bowl, Michael R.; Brown, Steven D. M.; Avan, Paul; Petit, Christine; El-Amraoui, Aziz
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