Treffer 1 - 11 von 11 für Suche 'KIRMANI, Mohammad H', Suchdauer: 0,57s Treffer weiter einschränken
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    AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders von Salpietro, Vincenzo, Guo, Hui, Bello, Oscar D, Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Torti, Erin, Rankin, Julia, Tariq, Huma, Pisani, Laura, Männikkö, Roope, Manole, Andreea, Ferrero, Giovanni Battista, Armstrong, Judith, Person, Richard E, Yoo, Kristin, Wang, Tianyun, Blesson, Alyssa, Jaeger, Bregje, Schneider, Amy L, Boysen, Katja, Myers, Candance T, Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W, Dyment, David, Osmond, Matthew, Van Haeringen, Arie, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Fabretto, Antonella, Hostettler, Isabel Charlotte, Yau, Wai Y, Chelban, Viorica, Diana, Maria C, Vari, Maria S, Bruno, Claudio, Scala, Marcello, Fiorillo, Chiara, Zanetti, Maria N, Krishnakumar, Shyam S, Madia, Francesca, Traverso, Monica, De-Marco, Patrizia, El-Khorassani, Mohamed, Karashova, Blagovesta, Tincheva, Radka, Gagliano, Antonella, Amadori, Elisabetta, Ibrahim, Shahnaz, Jan, Farida, Mine, Jun, Zuccotti, Gian V, Verrotti, Alberto, Marseglia, Gian Luigi, Savasta, Salvatore, Gitto, Eloisa, Sallemi, Alessia, Ruggieri, Martino, Mencacci, Niccolò Emanuele, Gupta, Neerja, Zamba-Papanicolaou, Eleni, Dardiotis, Efthimios, Maqbool, Shazia, Rana, Nuzhat, Lim, Shen Y, Al-Mutairi, Fuad, Ferrucci, Veronica, Zollo, Massimo, Alkuraya, Fowzan S, Kinali, Maria, Turki, Ilhem B. Y, Tazir, Meriem, Obeid, Makram, Bakhtadze, Sophia, Zaki, Maha, Triki, Chahnez C, Benfenati, Fabio, Capovilla, Giuseppe, Ojo, Oluwadamilola, Wahab, Kolawole Wasiu, Obiabo, Yahaya, Iyagba, Alagoma, Komolafe, Morenikeji, Senkevich, Konstantin, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Isrofilov, Maksud, Ramenghi, Luca A, Aguennouz, M'hammed, Tucci, Arianna, Fassi, Emily, De Zorzi, Rita, Kok, Fernando, Mefford, Heather C, Scheffer, Ingrid E, Universitat Autònoma de Barcelona

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    AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders von Salpietro, Vincenzo, Guo, Hui, Bello, Oscar D, Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Torti, Erin, Rankin, Julia, Tariq, Huma, Pisani, Laura, Männikkö, Roope, Manole, Andreea, Ferrero, Giovanni Battista, Armstrong, Judith, Person, Richard E, Yoo, Kristin, Wang, Tianyun, Blesson, Alyssa, Jaeger, Bregje, Schneider, Amy L, Boysen, Katja, Myers, Candance T, Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W, Dyment, David, Osmond, Matthew, Van Haeringen, Arie, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Fabretto, Antonella, Hostettler, Isabel Charlotte, Yau, Wai Y, Chelban, Viorica, Diana, Maria C, Vari, Maria S, Bruno, Claudio, Scala, Marcello, Fiorillo, Chiara, Zanetti, Maria N, Krishnakumar, Shyam S, Madia, Francesca, Traverso, Monica, De-Marco, Patrizia, El-Khorassani, Mohamed, Karashova, Blagovesta, Tincheva, Radka, Gagliano, Antonella, Amadori, Elisabetta, Ibrahim, Shahnaz, Jan, Farida, Mine, Jun, Zuccotti, Gian V, Verrotti, Alberto, Marseglia, Gian Luigi, Savasta, Salvatore, Gitto, Eloisa, Sallemi, Alessia, Ruggieri, Martino, Mencacci, Niccolò Emanuele, Gupta, Neerja, Zamba-Papanicolaou, Eleni, Dardiotis, Efthimios, Maqbool, Shazia, Rana, Nuzhat, Lim, Shen Y, Al-Mutairi, Fuad, Ferrucci, Veronica, Zollo, Massimo, Alkuraya, Fowzan S, Kinali, Maria, Turki, Ilhem B. Y, Tazir, Meriem, Obeid, Makram, Bakhtadze, Sophia, Zaki, Maha, Triki, Chahnez C, Benfenati, Fabio, Capovilla, Giuseppe, Ojo, Oluwadamilola, Wahab, Kolawole Wasiu, Obiabo, Yahaya, Iyagba, Alagoma, Komolafe, Morenikeji, Senkevich, Konstantin, Shashkin, Chingiz, Zharkynbekova, Nazira, Koneyev, Kairgali, Isrofilov, Maksud, Ramenghi, Luca A, Aguennouz, M'hammed, Tucci, Arianna, Fassi, Emily, De Zorzi, Rita, Kok, Fernando, Mefford, Heather C, Scheffer, Ingrid E, Universitat Autònoma de Barcelona

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