Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Delobel Bruno"'
Autor:
Nguyen, Tuan-Tu, Xu, Jiahui, Su, Zeliang, De Andrade, Vincent, Franco, Alejandro A., Delobel, Bruno, Delacourt, Charles, Demortière, Arnaud
In this study, we present a well-defined methodology for conducting Operando X-ray absorption near-edge structure spectroscopy (XANES) in conjunction with transmission X-ray nano computed tomography (TXM-nanoCT) experiments on the LiNi$_{0.5}$Mn$_{0.
Externí odkaz:
http://arxiv.org/abs/2307.08871
Autor:
Yang, Fang, Begemann, Anais, Reichhart, Nadine, Haeckel, Akvile, Steindl, Katharina, Schellenberger, Eyk, Sturm, Ronja Fini, Barth, Magalie, Bassani, Sissy, Boonsawat, Paranchai, Courtin, Thomas, Delobel, Bruno, Gunning, Boudewijn, Hardies, Katia, Jennesson, Mélanie, Legoff, Louis, Linnankivi, Tarja, Prouteau, Clément, Smal, Noor, Spodenkiewicz, Marta, Toelle, Sandra P., Van Gassen, Koen, Van Paesschen, Wim, Verbeek, Nienke, Ziegler, Alban, Zweier, Markus, Horn, Anselm H.C., Sticht, Heinrich, Lerche, Holger, Weckhuysen, Sarah, Strauß, Olaf, Rauch, Anita
Publikováno v:
In The American Journal of Human Genetics 6 June 2024 111(6):1184-1205
Autor:
Lacombe Didier, Mom Thierry, Francannet Christine, Duvillard Alain, Thauvin Christel, Dubin Jacques, Bonneau Dominique, Montaut-Verient Bettina, Vigneron Jacqueline, Calais Catherine, David Albert, Eliot Marie-Madeleine, Dollfus Hélène, Vincent Christophe, Delobel Bruno, Weil Dominique, El-Amraoui Aziz, Jonard Laurence, Feldmann Delphine, Zelenika Diana, Délépine Marc, Niasme-Grare Magali, Parodi Marine, Hardelin Jean-Pierre, Levilliers Jacqueline, Marlin Sandrine, Grati M'hamed, Bonnet Crystel, Duriez Françoise, Drouin-Garraud Valérie, Thuillier-Obstoy Marie-Françoise, Sigaudy Sabine, Frances Anne-Marie, Collignon Patrick, Challe Georges, Couderc Rémy, Lathrop Mark, Sahel José-Alain, Weissenbach Jean, Petit Christine, Denoyelle Françoise
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 21 (2011)
Abstract Background Usher syndrome (USH) combines sensorineural deafness with blindness. It is inherited in an autosomal recessive mode. Early diagnosis is critical for adapted educational and patient management choices, and for genetic counseling. T
Externí odkaz:
https://doaj.org/article/ac2297d1b7c045a391f3cfa701afae08
Autor:
Bloch, Adrien, Couture, Guillaume, Isidor, Bertrand, Ricquebourg, Manon, Bourrat, Emmanuelle, Lipsker, Dan, Taillan, Bruno, Combier, Alice, Chiaverini, Christine, Moufle, Frédérique, Delobel, Bruno, Richette, Pascal, Collet, Corinne
Publikováno v:
In European Journal of Medical Genetics February 2023 66(2)
Autor:
Pennamen, Perrine, Le, Linh, Tingaud-Sequeira, Angèle, Fiore, Mathieu, Bauters, Anne, Van Duong Béatrice, Nguyen, Coste, Valentine, Bordet, Jean-Claude, Plaisant, Claudio, Diallo, Modibo, Michaud, Vincent, Trimouille, Aurélien, Lacombe, Didier, Lasseaux, Eulalie, Delevoye, Cédric, Picard, Fanny Morice, Delobel, Bruno, Marks, Michael S., Arveiler, Benoit
Publikováno v:
In Genetics in Medicine October 2020 22(10):1613-1622
Publikováno v:
In Electrochimica Acta 1 February 2019 295:787-800
Akademický článek
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Autor:
Montagne, Louise, Derhourhi, Mehdi, Piton, Amélie, Toussaint, Bénédicte, Durand, Emmanuelle, Vaillant, Emmanuel, Thuillier, Dorothée, Gaget, Stefan, De Graeve, Franck, Rabearivelo, Iandry, Lansiaux, Amélie, Lenne, Bruno, Sukno, Sylvie, Desailloud, Rachel, Cnop, Miriam, Nicolescu, Ramona, Cohen, Lior, Zagury, Jean-François, Amouyal, Mélanie, Weill, Jacques, Muller, Jean, Sand, Olivier, Delobel, Bruno, Froguel, Philippe, Bonnefond, Amélie
Publikováno v:
In Molecular Metabolism July 2018 13:1-9
Publikováno v:
In Journal of Power Sources 1 March 2017 343:338-344
Autor:
Lanvin, Pierre‐Louis, Goronflot, Thomas, Isidor, Bertrand, Nizon, Mathilde, Durand, Benjamin, El Chehadeh, Salima, Geneviève, David, Ruault, Valentin, Fradin, Mélanie, Pasquier, Laurent, Thévenon, Julien, Delobel, Bruno, Burglen, Lydie, Afenjar, Alexandra, Faivre, Laurence, Francannet, Christine, Guerrot, Anne‐Marie, Goldenberg, Alice, Mercier, Sandra, Héron, Delphine
Publikováno v:
American Journal of Medical Genetics. Part A; Jan2024, Vol. 194 Issue 1, p9-16, 8p