Hakutulokset - Datta, Alexandre

Caffeine preserves quiet sleep in preterm neonates Tekijä Koch, Gilbert, Schönfeld, Natalie, Jost, Kerstin, Atkinson, Andrew, Schulzke, Sven M., Pfister, Marc, Datta, Alexandre N.

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Dynamics and complexity of body temperature in preterm infants nursed in incubators Tekijä Jost, Kerstin, Pramana, Isabelle, Delgado-Eckert, Edgar, Kumar, Nitin, Datta, Alexandre N., Frey, Urs, Schulzke, Sven M.

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6-year course of sleep homeostasis in a case with epilepsy-aphasia spectrum disorder Tekijä Oser, Nadine, Hubacher, Martina, Nageleisen-Weiss, Annette, van Mierlo, Pieter, Huber, Reto, Weber, Peter, Bölsterli, Bigna K., Datta, Alexandre N.

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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 Tekijä Lemola, Sakari, Oser, Nadine, Urfer-Maurer, Natalie, Brand, Serge, Holsboer-Trachsler, Edith, Bechtel, Nina, Grob, Alexander, Weber, Peter, Datta, Alexandre N.

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Fingolimod in children with Rett syndrome: the FINGORETT study Tekijä 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

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Birth experience in newborn infants is associated with changes in nociceptive sensitivity Tekijä 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

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Personalised therapeutic management of epileptic patients guided by pathway-driven breath metabolomics Tekijä 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

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Co-therapy with S-adenosylmethionine and nicotinamide riboside improves t-cell survival and function in Arts Syndrome (PRPS1 deficiency) Tekijä 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

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MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention Tekijä 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

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De novo GABRG2 mutations associated with epileptic encephalopathies Tekijä 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

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The phenotypic spectrum of X‐linked, infantile onset ALG13‐related developmental and epileptic encephalopathy Tekijä 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.

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Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy Tekijä 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

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Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/− mice Tekijä 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

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The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood Tekijä 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

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Narcolepsy and adjuvanted pandemic influenza A (H1N1) 2009 vaccines – Multi-country assessment Tekijä 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.

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