Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Hans W. Moises"'
Autor:
Hans W Moises
Publikováno v:
eLS. :1-10
Schizophrenia is a brain disorder of unknown etiology. Brain imaging studies have revealed evidence for hypoperfusion of the frontal cortex (hypofrontality) and progressive brain volume reduction in schizophrenic patients. Mild cerebral ischemia (oli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3a4eb80f8489d2bdd58d50f87f98b70
Autor:
Hans W. Moises
Publikováno v:
European Archives of Psychiatry and Clinical Neuroscience. 266:581-582
Autor:
Fritz Henn, Ralf M. Frieboes, Xiehe Liu, Liu Yang, Fabio Macciardi, P. Vetter, Hai G. Hwu, Hans W. Moises, Tao Li, Wagner F. Gattaz
Publikováno v:
American Journal of Medical Genetics. 105:246-249
The well-established role of genetic factors in the etiology of schizophrenia together with reports of allelic association with cPLA2, a phospholipase-A 2 gene, a reported increase of phospholipase-A 2 activity, and the phospholipase-A 2 hypothesis o
Publikováno v:
Scopus-Elsevier
Fifty-five hospital-treated patients with the ICD-10 diagnosis of recurrent depressive episode(s) were classified according to the Newcastle Depressive Diagnostic Scale as having either psychogenic (n = 25) or endogenous (n = 30) depression and inter
Autor:
Olaf Köller, Peter Kropp, Wulf D. Möller, P. Vetter, Olaf Steiner, Stefan Krauss, Hans W. Moises
Publikováno v:
Scopus-Elsevier
Objectives. We investigated homecare patients with dementia of Alzheimer's type (DAT; n = 36) or vascular dementia (VD; n = 36) and their care-providing relatives regarding clinical and psychosocial variables to determine whether DAT and VD impose di
Autor:
Derek J. Nancarrow, G Kalsi, Dermot Walsh, Hugh Gurling, J Brynjolfsson, Hannes Petursson, Jeremy M. Silverman, Kenneth S. Kendler, Robin M. Murray, T. d'Amato, Lynn R. Goldin, Hiroshi Kunugi, Robert B. Freedman, M. Jay, T. Sigmundson, W. Muri, Wolfgang Maier, William Byerley, J. Mallet, L. Yang, A. E. Pulver, C J MacLean, P. C. Sham, L. He, Raymond R. Crowe, R. E. Straub, Margot Albus, Dominique Campion, Michael John Owen, Richard P. Ebstein, Elliot S. Gershon, H. Donis-Keller, Hans W. Moises, Gerald Nestadt, D. H. R. Blackwood, Haig H. Kazazian, D. StClair, Claudine Laurent, Joachim Hallmayer, Claudia Wiese, D. B. Wildenauer, Stylianos E. Antonarakis, Bryan J. Mowry, Michael Gill, Homero Vallada, David E. Housman, H. Kristbjarnarson, R. Lofthouse, C. M. Read, Shinichiro Nanko, Mihael H. Polymeropoulos, P. McGuffin, Nicholas K. Hayward, H-G Hwu, S. Bodeau-Pean, Manfred Ackenheil, B. Lerer, David A. Collier, Douglas F. Levinson, Hilary Coon, Lynn E. DeLisi, J. H. Zhao, David Curtis, S. Maguire
Publikováno v:
Schizophrenia Research. 32:115-121
Patients with schizophrenia rarely develop rheumatoid arthritis, an autoimmune disease that exhibits genetic association with the HLA DRB1*04 gene. We previously investigated the hypothesis that schizophrenia is negatively associated with DRB1*04, an
Autor:
Dieter B. Wildenauer, Sibylle G. Schwab, Margot Albus, Joachim Hallmayer, Bernard Lerer, Wolfgang Maier, Douglas Blackwood, Walter Muir, David St Clair, Stewart Morris, Hans W. Moises, Liu Yang, Helgi Kristbjarnarson, Tomas Helgason, Claudia Wiese, David A. Collier, Peter Holmans, Jo Daniels, Mark Rees, Philip Asherson, Queta Roberts, Alastair Cardno, Maria J. Arranz, Homero Vallada, David Ball, Hiroshi Kunugi, Robin M. Murray, John F. Powell, Sin Nanko, Pak Sham, Mike Gill, Peter McGuffin, Michael J. Owen, Ann E. Pulver, Stylianos E. Antonarakis, Robert Babb, Jean-Louis Blouin, Nicola DeMarchi, Beth Dombroski, David Housman, Maria Karayiorgou, Jurg Ott, Laura Kasch, Haig Kazazian, Virginia K. Lasseter, Erika Loetscher, Hermann Luebbert, Gerald Nestadt, Carl Ton, Paula S. Wolyniec, Claudine Laurent, Michel de Chaldee, Florence Thibaut, Maurice Jay, Daniele Samolyk, Michel Petit, Dominique Campion, Jacques Mallet, Richard E. Straub, Charles J. MacLean, Stephen M. Easter, F. Anthony O'Neill, Dermot Walsh, Kenneth S. Kendler, Pablo V. Gejman, Qiuhe Cao, Elliot Gershon, Judith Badner, Ethiopia Beshah, Jing Zhang, Brien P. Riley, Swarnageetha Rajagopalan, Mpala Mogudi-Carter, Trefor Jenkins, Robert Williamson, Lynn E. DeLisi, Chad Garner, Mary Kelly, Carrie LeDuc, Lon Cardon, Jay Lichter, Tim Harris, Josephine Loftus, Gail Shields, Margarite Comasi, Antonio Vita, Angela Smith, Jay Dann, Geoff Joslyn, Hugh Gurling, Gursharan Kalsi, Jon Brynjolfsson, David Curtis, Thordur Sigmundsson, Robert Butler, Tim Read, Patrice Murphy, Andrew Chih-Hui Chen, Hannes Petursson, Bill Byerley, Mark Hoff, John Holik, Hilary Coon, Douglas F. Levinson, Derek J. Nancarrow, Raymond R. Crowe, Nancy Andreasen, Jeremy M. Silverman, Richard C. Mohs, Larry J. Siever, Jean Endicott, Lawrence Sharpe, Marilyn K. Walters, David P. Lennon, Nicholas K. Hayward, Lodewijk A. Sandkuijl, Bryan J. Mowry, Harald N. Aschauer, Kurt Meszaros, Elisabeth Lenzinger, Karoline Fuchs, Angela M. Heiden, Leonid Kruglyak, Mark J. Daly, Tara C. Matise
Publikováno v:
American Journal of Medical Genetics. 67:580-594
In response to reported schizophrenia linkage findings on chromosomes 3, 6 and 8, fourteen research groups genotyped 14 microsatellite markers in an unbiased, collaborative (New) sample of 403-567 informative pedigrees per marker, and in the Original
Autor:
Michael Gill, Homero Vallada, David Collier, Pak Sham, Peter Holmans, Robin Murray, Peter McGuffin, Shin Nanko, Mike Owen, Stylianos Antonarakis, David Housman, Haig Kazazian, Gerald Nestadt, Ann E. Pulver, Richard E. Straub, Charles J. MacLean, Dermot Walsh, Kenneth S. Kendler, Lynn DeLisi, Mihael Polymeropoulos, Hilary Coon, William Byerley, Ray Lofthouse, Elliot Gershon, Lynn Golden, Timothy Crow, Robert Freedman, Claudine Laurent, Sylvie Bodeau-Pean, Thierry d'Amato, Maurice Jay, Dominique Campion, Jacques Mallet, Dieter B. Wildenauer, Bernard Lerer, Margot Albus, Manfred Ackenheil, Richard P. Ebstein, Joachim Hallmayer, Wolfgang Maier, Hugh Gurling, David Curtis, Gusharon Kalsi, Jon Brynjolfsson, Thordur Sigmundson, Hannes Petursson, Douglas Blackwood, Walter Muir, David St. Clair, Lin He, Susan Maguire, Hans W. Moises, Hai-Gwo Hwu, Liu Yang, Claudia Wiese, Li Tao, Xiehe Liu, Helgi Kristbjarnason, Douglas F. Levinson, Bryan J. Mowry, Helen Donis-Keller, Nicholas K. Hayward, Raymond R. Crowe, Jeremy M. Silverman, Derek J. Nancarrow, Christina M. Read
Publikováno v:
American Journal of Medical Genetics. 67:40-45
Several groups have reported weak evidence for linkage between schizophrenia and genetic markers located on chromosome 22q using the lod score method of analysis. However these findings involved different genetic markers and methods of analysis, and
Autor:
Tao Li, Claudia Wiese, Xiehe Liu, Pierre Sokoloff, Jean-Charles Schwartz, Chong T. Xu, Hans W. Moises, Zhong Zeng, Liu Yang, Lars Lannfelt
Publikováno v:
Scopus-Elsevier
The D3 dopamine receptor gene is an important candidate gene for schizophrenia, since (because of its almost exclusive expression in the limbic system) it combines the dopamine receptor hypothesis with the limbic system hypothesis of schizophrenia. A