Resultados de búsqueda - Datta, Alexandre
- Mostrando 1 - 15 Resultados de 15
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6-year course of sleep homeostasis in a case with epilepsy-aphasia spectrum disorder por Oser, Nadine, Hubacher, Martina, Nageleisen-Weiss, Annette, van Mierlo, Pieter, Huber, Reto, Weber, Peter, Bölsterli, Bigna K., Datta, Alexandre N.
Publicado 2021Texto -
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Effects of gestational age on brain volume and cognitive functions in generally healthy very preterm born children during school-age: A voxel-based morphometry study por Lemola, Sakari, Oser, Nadine, Urfer-Maurer, Natalie, Brand, Serge, Holsboer-Trachsler, Edith, Bechtel, Nina, Grob, Alexander, Weber, Peter, Datta, Alexandre N.
Publicado 2017Texto -
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Fingolimod in children with Rett syndrome: the FINGORETT study por Naegelin, Yvonne, Kuhle, Jens, Schädelin, Sabine, Datta, Alexandre N., Magon, Stefano, Amann, Michael, Barro, Christian, Ramelli, Gian Paolo, Heesom, Kate, Barde, Yves-Alain, Weber, Peter, Kappos, Ludwig
Publicado 2021Texto -
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Birth experience in newborn infants is associated with changes in nociceptive sensitivity por Kasser, Severin, Hartley, Caroline, Rickenbacher, Hanna, Klarer, Noemi, Depoorter, Antoinette, Datta, Alexandre N., Cobo, Maria M., Goksan, Sezgi, Hoskin, Amy, Magerl, Walter, Huhn, Evelyn A., Green, Gabrielle, Slater, Rebeccah, Wellmann, Sven
Publicado 2019Texto -
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Personalised therapeutic management of epileptic patients guided by pathway-driven breath metabolomics por Singh, Kapil Dev, Osswald, Martin, Ziesenitz, Victoria C., Awchi, Mo, Usemann, Jakob, Imbach, Lukas L., Kohler, Malcolm, García-Gómez, Diego, van den Anker, Johannes, Frey, Urs, Datta, Alexandre N., Sinues, Pablo
Publicado 2021Texto -
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Co-therapy with S-adenosylmethionine and nicotinamide riboside improves t-cell survival and function in Arts Syndrome (PRPS1 deficiency) por Lenherr, Nina, Christodoulou, John, Duley, John, Dobritzsch, Doreen, Fairbanks, Lynette, Datta, Alexandre N., Filges, Isabel, Gürtler, Nicolas, Roelofsen, Jeroen, van Kuilenburg, André B.P., Kemper, Claudia, West, Erin E., Szinnai, Gabor, Huemer, Martina
Publicado 2021Texto -
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MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention por Tischner, Christin, Hofer, Annette, Wulff, Veronika, Stepek, Joanna, Dumitru, Iulia, Becker, Lore, Haack, Tobias, Kremer, Laura, Datta, Alexandre N., Sperl, Wolfgang, Floss, Thomas, Wurst, Wolfgang, Chrzanowska-Lightowlers, Zofia, De Angelis, Martin Hrabe, Klopstock, Thomas, Prokisch, Holger, Wenz, Tina
Publicado 2015Texto -
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De novo GABRG2 mutations associated with epileptic encephalopathies por Shen, Dingding, Hernandez, Ciria C, Shen, Wangzhen, Hu, Ningning, Poduri, Annapurna, Shiedley, Beth, Rotenberg, Alex, Datta, Alexandre N, Leiz, Steffen, Patzer, Steffi, Boor, Rainer, Ramsey, Kerri, Goldberg, Ethan, Helbig, Ingo, Ortiz-Gonzalez, Xilma R, Lemke, Johannes R, Marsh, Eric D, Macdonald, Robert L
Publicado 2017Texto -
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The phenotypic spectrum of X‐linked, infantile onset ALG13‐related developmental and epileptic encephalopathy por Datta, Alexandre N., Bahi‐Buisson, Nadia, Bienvenu, Thierry, Buerki, Sarah E., Gardiner, Fiona, Cross, J. Helen, Heron, Bénédicte, Kaminska, Anna, Korff, Christian M., Lepine, Anne, Lesca, Gaetan, McTague, Amy, Mefford, Heather C., Mignot, Cyrill, Milh, Matthieu, Piton, Amélie, Pressler, Ronit M., Ruf, Susanne, Sadleir, Lynette G., de Saint Martin, Anne, Van Gassen, Koen, Verbeek, Nienke E., Ville, Dorothée, Villeneuve, Nathalie, Zacher, Pia, Scheffer, Ingrid E., Lemke, Johannes R.
Publicado 2021Texto -
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Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy por Vegas, Nancy, Cavallin, Mara, Maillard, Camille, Boddaert, Nathalie, Toulouse, Joseph, Schaefer, Elise, Lerman-Sagie, Tally, Lev, Dorit, Magalie, Barth, Moutton, Sébastien, Haan, Eric, Isidor, Bertrand, Heron, Delphine, Milh, Mathieu, Rondeau, Stéphane, Michot, Caroline, Valence, Stephanie, Wagner, Sabrina, Hully, Marie, Mignot, Cyril, Masurel, Alice, Datta, Alexandre, Odent, Sylvie, Nizon, Mathilde, Lazaro, Leila, Vincent, Marie, Cogné, Benjamin, Guerrot, Anne Marie, Arpin, Stéphanie, Pedespan, Jean Michel, Caubel, Isabelle, Pontier, Benedicte, Troude, Baptiste, Rivier, Francois, Philippe, Christophe, Bienvenu, Thierry, Spitz, Marie-Aude, Bery, Amandine, Bahi-Buisson, Nadia
Publicado 2018Texto -
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Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/− mice por Pringsheim, Milka, Mitter, Diana, Schröder, Simone, Warthemann, Rita, Plümacher, Kim, Kluger, Gerhard, Baethmann, Martina, Bast, Thomas, Braun, Sarah, Büttel, Hans‐Martin, Conover, Elizabeth, Courage, Carolina, Datta, Alexandre N., Eger, Angelika, Grebe, Theresa A., Hasse‐Wittmer, Annette, Heruth, Marion, Höft, Karen, Kaindl, Angela M., Karch, Stephanie, Kautzky, Torsten, Korenke, Georg C., Kruse, Bernd, Lutz, Richard E., Omran, Heymut, Patzer, Steffi, Philippi, Heike, Ramsey, Keri, Rating, Tina, Rieß, Angelika, Schimmel, Mareike, Westman, Rachel, Zech, Frank‐Martin, Zirn, Birgit, Ulmke, Pauline A., Sokpor, Godwin, Tuoc, Tran, Leha, Andreas, Staudt, Martin, Brockmann, Knut
Publicado 2019Texto -
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The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood por Döring, Jan Henje, Saffari, Afshin, Bast, Thomas, Brockmann, Knut, Ehrhardt, Laura, Fazeli, Walid, Janzarik, Wibke G., Kluger, Gerhard, Muhle, Hiltrud, Møller, Rikke S., Platzer, Konrad, Santos, Joana Larupa, Bache, Iben, Bertsche, Astrid, Bonfert, Michaela, Borggräfe, Ingo, Broser, Philip J., Datta, Alexandre N., Hammer, Trine Bjørg, Hartmann, Hans, Hasse-Wittmer, Anette, Henneke, Marco, Kühne, Hermann, Lemke, Johannes R., Maier, Oliver, Matzker, Eva, Merkenschlager, Andreas, Opp, Joachim, Patzer, Steffi, Rostasy, Kevin, Stark, Birgit, Strzelczyk, Adam, von Stülpnagel, Celina, Weber, Yvonne, Wolff, Markus, Zirn, Birgit, Hoffmann, Georg Friedrich, Kölker, Stefan, Syrbe, Steffen
Publicado 2020Texto -
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Narcolepsy and adjuvanted pandemic influenza A (H1N1) 2009 vaccines – Multi-country assessment por Weibel, Daniel, Sturkenboom, Miriam, Black, Steven, de Ridder, Maria, Dodd, Caitlin, Bonhoeffer, Jan, Vanrolleghem, Ann, van der Maas, Nicoline, Lammers, Gert Jan, Overeem, Sebastiaan, Gentile, Angela, Giglio, Norberto, Castellano, Vanesa, Kwong, Jeffrey C., Murray, Brian J., Cauch-Dudek, Karen, Juhasz, Diana, Campitelli, Michael, Datta, Alexandre N., Kallweit, Ulf, Huang, Wan-Ting, Huang, Yu-Shu, Hsu, Chung-Yao, Chen, Hsi-Chung, Giner-Soriano, Maria, Morros, Rosa, Gaig, Carles, Tió, Ester, Perez-Vilar, Silvia, Diez-Domingo, Javier, Puertas, Francisco Javier, Svenson, Lawrence W., Mahmud, Salaheddin M., Carleton, Bruce, Naus, Monika, Arnheim-Dahlström, Lisen, Pedersen, Lars, DeStefano, Frank, Shimabukuro, Tom T.
Publicado 2018Texto