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TITLE: Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment  Full Text
AUTHORS: Jonard, Laurence; Brotto, Davide; Moreno Pelayo, Miguel A.; del Castillo, Ignacio; Kremer, Hannie; Pennings, Ronald; Caria, Helena; Fialho, Graca; Boudewyns, An; Van Camp, Guy; Oldak, Monika; Ozieblo, Dominika; Deggouj, Naima; De Siati, Romolo Daniele; Gasparini, Paolo; Girotto, Giorgia; Verstreken, Margriet; Dossena, Silvia; Roesch, Sebastian; Battelino, Saba; Trebusak Podkrajsek, Katarina; Warnecke, Athanasia; Lenarz, Thomas; Lesinski Schiedat, Anke; Mondain, Michel; Roux, Anne Francoise; Denoyelle, Francoise; Loundon, Natalie; Serey Gaut, Margaux; Trevisi, Patrizia; Rubinato, Elisa; Martini, Alessandro; Marlin, Sandrine; ...More
PUBLISHED: 2023, SOURCE: AUDIOLOGY RESEARCH, VOLUME: 13, ISSUE: 3
INDEXED IN: Scopus WOS
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TITLE: Contemporary European practice in transcatheter aortic valve implantation: results from the 2022 European TAVI Pathway Registry
AUTHORS: Rosseel, Liesbeth; Mylotte, Darren; Cosyns, Bernard; Vanhaverbeke, Maarten; Zweiker, David; Teles, Rui Campante; Angeras, Oskar; Neylon, Antoinette; Rudolph, Tanja Katharina; Wykrzykowska, Joanna J.; Patterson, Tiffany; Costa, Giulia; Ojeda, Soledad; Tzikas, Apostolos; Abras, Marcel; Leroux, Lionel; Van Belle, Eric; Tchetche, Didier; Bleiziffer, Sabine; Swaans, Martin J.; Parma, Radoslaw; Blackman, Daniel J.; Van Mieghem, Nicolas M.; Grygier, Marek; Redwood, Simon; Prendergast, Bernard; Van Camp, Guy; De Backer, Ole; ...More
PUBLISHED: 2023, SOURCE: FRONTIERS IN CARDIOVASCULAR MEDICINE, VOLUME: 10
INDEXED IN: Scopus WOS
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TITLE: Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene  Full Text
AUTHORS: Nele Hilgert; Matthew J Huentelman; Ashley Q Thorburn; Erik Fransen; Nele Dieltjens; Malgorzata Mueller Malesinska; Agnieszka Pollak; Agata Skorka; Jaroslaw Waligora; Rafal Ploski; Pierangela Castorina; Paola Primignani; Umberto Ambrosetti; Alessandra Murgia; Eva Orzan; Arti Pandya; Kathleen Arnos; Virginia Norris; Pavel Seeman; Petr Janousek; Delphine Feldmann; Sandrine Marlin; Francoise Denoyelle; Carla J Nishimura; Andreas Janecke; Doris Nekahm Heis; Alessandro Martini; Elena Mennucci; Timea Toth; Istvan Sziklai; Ignacio del Castillo; Felipe Moreno; Michael B Petersen; Vasiliki Iliadou; Mustafa Tekin; Armagan Incesulu; Ewa Nowakowska; Jerzy Bal; Paul Van de Heyning; Anne Francoise Roux; Catherine Blanchet; Cyril Goizet; Guenaelle Lancelot; Graca Fialho ; Helena Caria ; Xue Zhong Liu; Ouyang Y Xiaomei; Paul Govaerts; Karen Gronskov; Karianne Hostmark; Klemens Frei; Ingeborg Dhooge; Stephen Vlaeminck; Erdmute Kunstmann; Lut Van Laer; Richard J H Smith; Guy Van Camp; ...More
PUBLISHED: 2009, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 17, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef