Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Klaassen, Petra"'
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
Autor:
Duijff, Sasja, Klaassen, Petra, Beemer, Frits, Swanenburg de Veye, Henriette, Vorstman, Jacob, Sinnema, Gerben
Publikováno v:
In Research in Developmental Disabilities March-April 2012 33(2):334-340
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
Autor:
Klaassen, Petra, Duijff, Sasja, Swanenburg de Veye, Henriëtte, Beemer, Frits, Sinnema, Gerben, Breetvelt, Elemi, Schappin, Renske, Vorstman, Jacob
Publikováno v:
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics, 171(6), 790–796. Wiley-Liss Inc.
The role of rare genetic variants, in particular copy number variants (CNVs), in the etiology of neurodevelopmental disorders is becoming increasingly clear. While the list of these disorder-related CNVs continues to lengthen, it has also become clea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2bfd5f2bd033d96d471198f014394d31
https://dspace.library.uu.nl/handle/1874/346535
https://dspace.library.uu.nl/handle/1874/346535
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
Autor:
Schneider, Maude, Debbané, Martin, Bassett, Anne S, Chow, Eva WC, Fung, Wai Lun Alan, van den Bree, Marianne, Owen, Michael, Murphy, Kieran C, Niarchou, Maria, Kates, Wendy R, Antshel, Kevin M, Fremont, Wanda, McDonald-McGinn, Donna M, Gur, Raquel E, Zackai, Elaine H, Vorstman, Jacob, Duijff, Sasja N, Klaassen, Petra WJ, Swillen, Ann, Gothelf, Doron, Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R, Bearden, Carrie E, Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Murphy, Declan G, Ousley, Opal, Campbell, Linda E, Simon, Tony J, Eliez, Stephan, International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome
Publikováno v:
The American journal of psychiatry, vol 171, iss 6
Schneider, M; Debbane, M; Bassett, AS; Chow, EWC; Fung, WLA; van den Bree, MBM; et al.(2014). Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. AMERICAN JOURNAL OF PSYCHIATRY, 171(6), 627-639. doi: 10.1176/appi.ajp.2013.13070864. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/4wc7m96r
Schneider, M; Debbane, M; Bassett, AS; Chow, EWC; Fung, WLA; van den Bree, MBM; et al.(2014). Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. AMERICAN JOURNAL OF PSYCHIATRY, 171(6), 627-639. doi: 10.1176/appi.ajp.2013.13070864. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/4wc7m96r
ObjectiveChromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates of schizophrenia and other psychiatric conditions. The authors report what is to their knowledge the first large-scale collaborative study of rates an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a122227a30b71e3b9e0becf8caa3a6a9
https://escholarship.org/uc/item/4wc7m96r
https://escholarship.org/uc/item/4wc7m96r
Autor:
Owen, Michael, Swillen, Ann, Boot, Erik, Murphy, Kieran C., Green, Tamar, Klaassen, Petra W.J., Bassett, Anne S., Chow, Eva W.C., Antshel, Kevin M., Gur, Raquel E., Gothelf, Doron, Evers, Laurens, Duijff, Sasja N., van den Bree, Marianne B.M., Armando, Marco, Murphy, Declan G., Shashi, Vandana, Fremont, Wanda, Schneider, Maude, Vorstman, Jacob, Bearden, Carrie E., Fung, Wai Lun Alan, Vicari, Stefano, Hooper, Stephen R., Jalbrzikowski, Maria, Van Amelsvoort, Therese, Debbané, Martin, Zackai, Elaine H., McDonald-McGinn, Donna M., Kates, Wendy R., Niarchou, Maria, Weizman, Abraham
Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates of schizophrenia and other psychiatric conditions. The authors report what is to their knowledge the first large-scale collaborative study of rates and sex dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::491e66fad5e73e066e412590569eab1c
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