APA
Lemke J. R., Geider K., Helbig K. L., Heyne H. O., Schütz H., Hentschel J., Courage C., Depienne C., Nava C., Heron D., Møller R. S., Hjalgrim H., Lal D., Neubauer B. A., Nürnberg P., Thiele H., Kurlemann G., Arnold G. L., Bhambhani V., Bartholdi D., Pedurupillay C. R. J., Misceo D., Frengen E., Strømme P., Dlugos D. J., Doherty E. S., Bijlsma E. K., Ruivenkamp C. A., Hoffer M. J. V., Goldstein A., Rajan D. S., Narayanan V., Ramsey K., Belnap N., Schrauwen I., Richholt R., Koeleman B. P. C., Sá J., Mendonça C., de Kovel C. G. F., Weckhuysen S., Hardies K., De Jonghe P., De Meirleir L., Milh M., Badens C., Lebrun M., Busa T., Francannet C., Piton A., Riesch E., Biskup S., Vogt H., Dorn T., Helbig I., Michaud J. L., Laube B. & Syrbe S. (20170508). Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. : Neurology.
Chicago
Lemke Johannes R, Geider Kirsten, Helbig Katherine L, Heyne Henrike O, Schütz Hannah, Hentschel Julia, Courage Carolina, Depienne Christel, Nava Caroline, Heron Delphine, Møller Rikke S, Hjalgrim Helle, Lal Dennis, Neubauer Bernd A, Nürnberg Peter, Thiele Holger, Kurlemann Gerhard, Arnold Georgianne L, Bhambhani Vikas, Bartholdi Deborah, Pedurupillay Christeen Ramane J, Misceo Doriana, Frengen Eirik, Strømme Petter, Dlugos Dennis J, Doherty Emily S, Bijlsma Emilia K, Ruivenkamp Claudia A, Hoffer Mariette J V, Goldstein Amy, Rajan Deepa S, Narayanan Vinodh, Ramsey Keri, Belnap Newell, Schrauwen Isabelle, Richholt Ryan, Koeleman Bobby P C, Sá Joaquim, Mendonça Carla, de Kovel Carolien G F, Weckhuysen Sarah, Hardies Katia, De Jonghe Peter, De Meirleir Linda, Milh Mathieu, Badens Catherine, Lebrun Marine, Busa Tiffany, Francannet Christine, Piton Amélie, Riesch Erik, Biskup Saskia, Vogt Heinrich, Dorn Thomas, Helbig Ingo, Michaud Jacques L, Laube Bodo and Syrbe Steffen. 20170508. Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. : Neurology.
Harvard
Lemke J. R., Geider K., Helbig K. L., Heyne H. O., Schütz H., Hentschel J., Courage C., Depienne C., Nava C., Heron D., Møller R. S., Hjalgrim H., Lal D., Neubauer B. A., Nürnberg P., Thiele H., Kurlemann G., Arnold G. L., Bhambhani V., Bartholdi D., Pedurupillay C. R. J., Misceo D., Frengen E., Strømme P., Dlugos D. J., Doherty E. S., Bijlsma E. K., Ruivenkamp C. A., Hoffer M. J. V., Goldstein A., Rajan D. S., Narayanan V., Ramsey K., Belnap N., Schrauwen I., Richholt R., Koeleman B. P. C., Sá J., Mendonça C., de Kovel C. G. F., Weckhuysen S., Hardies K., De Jonghe P., De Meirleir L., Milh M., Badens C., Lebrun M., Busa T., Francannet C., Piton A., Riesch E., Biskup S., Vogt H., Dorn T., Helbig I., Michaud J. L., Laube B. and Syrbe S. (20170508). Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. : Neurology.
MLA
Lemke Johannes R, Geider Kirsten, Helbig Katherine L, Heyne Henrike O, Schütz Hannah, Hentschel Julia, Courage Carolina, Depienne Christel, Nava Caroline, Heron Delphine, Møller Rikke S, Hjalgrim Helle, Lal Dennis, Neubauer Bernd A, Nürnberg Peter, Thiele Holger, Kurlemann Gerhard, Arnold Georgianne L, Bhambhani Vikas, Bartholdi Deborah, Pedurupillay Christeen Ramane J, Misceo Doriana, Frengen Eirik, Strømme Petter, Dlugos Dennis J, Doherty Emily S, Bijlsma Emilia K, Ruivenkamp Claudia A, Hoffer Mariette J V, Goldstein Amy, Rajan Deepa S, Narayanan Vinodh, Ramsey Keri, Belnap Newell, Schrauwen Isabelle, Richholt Ryan, Koeleman Bobby P C, Sá Joaquim, Mendonça Carla, de Kovel Carolien G F, Weckhuysen Sarah, Hardies Katia, De Jonghe Peter, De Meirleir Linda, Milh Mathieu, Badens Catherine, Lebrun Marine, Busa Tiffany, Francannet Christine, Piton Amélie, Riesch Erik, Biskup Saskia, Vogt Heinrich, Dorn Thomas, Helbig Ingo, Michaud Jacques L, Laube Bodo and Syrbe Steffen. Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. : Neurology. 20170508.