Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Duijff, Sasja N"'
Autor:
Nijhof, Sanne L., Vinkers, Christiaan H., van Geelen, Stefan M., Duijff, Sasja N., Achterberg, E.J. Marijke, van der Net, Janjaap, Veltkamp, Remco C., Grootenhuis, Martha A., van de Putte, Elise M., Hillegers, Manon H.J., van der Brug, Anneke W., Wierenga, Corette J., Benders, Manon J.N.L., Engels, Rutger C.M.E., van der Ent, C. Kors, Vanderschuren, Louk J.M.J., Lesscher, Heidi M.B.
Publikováno v:
In Neuroscience and Biobehavioral Reviews December 2018 95:421-429
Publikováno v:
Advances in Neurodevelopmental Disorders; 20240101, Issue: Preprints p1-18, 18p
Autor:
Duijff, Sasja N., Klaassen, Petra W.J., Swanenburg de Veye, Henriëtte F.N., Beemer, Frits A., Sinnema, Gerben, Vorstman, Jacob A.S.
Publikováno v:
In Research in Developmental Disabilities September 2013 34(9):2937-2945
Akademický článek
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Autor:
Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S, Heung, Tracy, Holleman, Aaron M, Johnston, H Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M, Gur, Raquel E, Morrow, Bernice E, Swillen, Ann, Vorstman, Jacob AS, Bearden, Carrie E, Chow, Eva WC, van den Bree, Marianne, Emanuel, Beverly S, Vermeesch, Joris R, Warren, Stephen T, Owen, Michael J, Chopra, Pankaj, Cutler, David J, Duncan, Richard, Kotlar, Alex V, Mulle, Jennifer G, Voss, Anna J, Zwick, Michael E, Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I, Tran, Oanh, Holmans, Peter, Pardinas, Antonio, Walters, James TR, Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J, Costain, Gregory A, Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese AMJ, van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vergaelen, Elfi, Vogels, Annick, Crowley, T Blaine, McGinn, Daniel E, Moss, Edward M, Sharkus, Robert J, Unolt, Marta, Zackai, Elaine H, Calkins, Monica E, Gallagher, Robert S, Gur, Ruben C, Tang, Sunny X, Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M, Breetvelt, Elemi, Duijff, Sasja N, Fiksinski, Ania, Moss, Hayley, Niarchou, Maria, Murphy, Kieran C, Prasad, Sarah E, Daly, Eileen M, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan G, Buzzanca, Antonio, Fabio, Fabio Di, Digilio, Maria C, Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F, Ousley, Opal Y, Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Schneider, Maude
Publikováno v:
Molecular psychiatry, vol 26, iss 8
Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::32f66e4eba32686804f3949cd756407d
https://escholarship.org/uc/item/1wx189cs
https://escholarship.org/uc/item/1wx189cs
Autor:
VORSTMAN, JACOB A.S., MORCUS, MONIQUE E.J., DUIJFF, SASJA N., KLAASSEN, PETRA W.J., HEINEMAN-de BOER, JOSIEN A., BEEMER, FRITS A., SWAAB, HANNA, KAHN, RENÉ S., van ENGELAND, HERMAN
Publikováno v:
In Journal of the American Academy of Child & Adolescent Psychiatry September 2006 45(9):1104-1113
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Sommer, Iris E, Bearden, Carrie E, van Dellen, Edwin, Breetvelt, Elemi J, Duijff, Sasja N, Maijer, Kim, van Amelsvoort, Therese, de Haan, Lieuwe, Gur, Raquel E, Arango, Celso, Díaz-Caneja, Covadonga M, Vinkers, Christiaan H, Vorstman, Jacob As
Publikováno v:
NPJ schizophrenia, vol 2, iss 1
Intervention strategies in adolescents at ultra high-risk (UHR) for psychosis are promising for reducing conversion to overt illness, but have only limited impact on functional outcome. Recent studies suggest that cognition does not further decline d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::95a437d52befd0360a46f3e67885cb98
https://escholarship.org/uc/item/6zp409s6
https://escholarship.org/uc/item/6zp409s6
Autor:
Vorstman, Jacob A S, Breetvelt, Elemi J., Duijff, Sasja N., Eliez, Stephan, Schneider, Maude, Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Shashi, Vandana, Hooper, Stephen R., Chow, Eva W C, Fung, Wai Lun Alan, Butcher, Nancy J., Young, Donald A., McDonald-McGinn, Donna M., Vogels, Annick, Van Amelsvoort, Therese, Gothelf, Doron, Weinberger, Ronnie, Weizman, Abraham, Klaassen, Petra W J, Koops, Sanne, Kates, Wendy R., Antshel, Kevin M., Simon, Tony J., Ousley, Opal Y., Swillen, Ann, Gur, Raquel E., Bearden, Carrie E., Kahn, René S., Bassett, Anne S., Emanuel, Beverly S., Zackai, Elaine H., Kushan, Leila, Fremont, Wanda, Schoch, Kelly, Stoddard, Joel, Cubells, Joseph, Fu, Fiona, Campbell, Linda E., Fritsch, Rosemarie, Vergaelen, Elfi, Neeleman, Marjolein, Boot, Erik, Debbané, Martin, Philip, Nicole, Green, Tamar, Van DenBree, Marianne B M, Murphy, Declan, Canyelles, Jaume Morey, Arango, Celso, Murphy, Kieran C., Pontillo, Maria
Publikováno v:
Vorstman, JAS; Breetvelt, EJ; Duijff, SN; Eliez, S; Schneider, M; Jalbrzikowski, M; et al.(2015). Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. JAMA Psychiatry, 72(4), 377-385. doi: 10.1001/jamapsychiatry.2014.2671. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/9rb845gn
JAMA psychiatry, vol 72, iss 4
JAMA Psychiatry, 72(4), 377. American Medical Association
JAMA Psychiatry, 72(4), 377-385. American Medical Association
JAMA Psychiatry, Vol. 72, No 4 (2015) pp. 377-85
JAMA psychiatry, vol 72, iss 4
JAMA Psychiatry, 72(4), 377. American Medical Association
JAMA Psychiatry, 72(4), 377-385. American Medical Association
JAMA Psychiatry, Vol. 72, No 4 (2015) pp. 377-85
© 2015 American Medical Association. All rights reserved. Importance: Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of developing schizophrenia. Recent reports have suggested that a subgroup of children with 22q11DS d