Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Raeymaekers, Peter"'
Autor:
Chumakov, Ilya, Blumenfeld, Marta, Guerassimenko, Oxana, Cavarec, Laurent, Palicio, Marta, Abderrahim, Hadi, Bougueleret, Lydie, Barry, Caroline, Tanaka, Hiroaki, La Rosa, Philippe, Puech, Anne, Tahri, Nadia, Cohen-Akenine, Annick, Delabrosse, Sylvain, Lissarrague, Sébastien, Picard, Françoise-Pascaline, Maurice, Karelle, Essioux, Laurent, Millasseau, Philippe, Grel, Pascale, Debailleul, Virginie, Simon, Anne-Marie, Caterina, Dominique, Dufaure, Isabelle, Malekzadeh, Kattayoun, Belova, Maria, Luan, Jian-Jian, Bouillot, Michel, Sambucy, Jean-Luc, Primas, Gwenael, Saumier, Martial, Boubkiri, Nadia, Martin-Saumier, Sandrine, Nasroune, Myriam, Peixoto, Hélène, Delaye, Arnaud, Pinchot, Virginie, Bastucci, Mariam, Guillou, Sophie, Chevillon, Magali, Sainz-Fuertes, Ricardo, Meguenni, Said, Aurich-Costa, Joan, Cherif, Dorra, Gimalac, Anne, van Duijn, Cornelia, Gauvreau, Denis, Ouelette, Gail, Fortier, Isabel, Realson, John, Sherbatich, Tatiana, Riazanskaia, Nadejda, Rogaev, Evgeny, Raeymaekers, Peter, Aerssens, Jeroen, Konings, Frank, Luyten, Walter, Macciardi, Fabio, Sham, Pak C., Straub, Richard E., Weinberger, Daniel R., Cohen, Nadine, Cohen, Daniel
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2002 Oct . 99(21), 13675-13680.
Externí odkaz:
https://www.jstor.org/stable/3073467
Autor:
Claes, Stephan, Devriendt, K., Van Goethem, Gert, Roelen, L., Meireleire, J., Raeymaekers, Peter, Cassiman, J.J., Fryns, J.P.
Publikováno v:
American journal of medical genetics
Autor:
Massat, Isabelle, Souery, Daniel, Lipp, Olivier, Verheyen, Geert, Raeymaekers, Peter, Van Broeckhoven, Christine
Publikováno v:
American journal of medical genetics
The available data on the role of 5-HT in a variety of behaviors support the hypothesis that a dysfunction in brain serotoninergic system activity contributes to vulnerability to major depression. The diversity in the electrophysiological actions of
Autor:
Van Goethem, Gert, Löfgren, Ann, Raeymaekers, Peter, Martin, Jean-Jacques, Van Broeckhoven, Christine
Publikováno v:
Journal of medical genetics
Editor—Disorders of oxidative phosphorylation are highly heterogeneous from both a clinical and a genetic point of view. The nuclear as well as the mitochondrial genomes contain genes that are necessary for respiratory chain function. Consequently,
Publikováno v:
Journal of medical genetics
Usher syndrome is a group of autosomal recessive disorders characterised by progressive visual loss from retinitis pigmentosa and moderate to severe sensorineural hearing loss. Usher syndrome is estimated to account for 6-10% of all congenital sensor
Autor:
Verheyen, Geert, Villafuerte, S.M., Del-Favero, Jurgen, Souery, D., Mendlewicz, J., Raeymaekers, Peter, Van Broeckhoven, Christine
Publikováno v:
European journal of human genetics
Autor:
Verheyen, Geert, Del-Favero, Jurgen, Oruč, L., Raeymaekers, Peter, Van Broeckhoven, Christine
Publikováno v:
Neuroscience news
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2097::2fb6af5e784dc1791c483dbdefa0b11e
https://hdl.handle.net/10067/194040151162165141
https://hdl.handle.net/10067/194040151162165141
Autor:
Claes, Stephan, Aguirre, T., Simosa, V., Bustos, T., Lander, R., Piras, M., Legius, E., Cassiman, J.J., Raeymaekers, Peter
Publikováno v:
Human mutation
Publikováno v:
De agenda van de specialist. Psychiatrie.
Autor:
Oruč, L., Verheyen, Geert, Fura·, I., Jakovljevič, M., Iveziµ, I., Raeymaekers, Peter, Van Broeckhoven, Christine
Publikováno v:
American journal of medical genetics