Zobrazeno 1 - 5
of 5
pro vyhledávání: '"G. A. van Wingen"'
Autor:
M. S. Oudijn, J. T. W. Linders, A. Lok, P. R. Schuurman, P. van den Munckhof, A. A. van Elburg, G. A. van Wingen, R. J. T. Mocking, D. Denys
Publikováno v:
Journal of Eating Disorders, Vol 11, Iss 1, Pp 1-12 (2023)
Abstract Background Anorexia nervosa (AN) is a severe and life-threatening psychiatric disorder. Initial studies on deep brain stimulation (DBS) in severe, treatment-refractory AN have shown clinical effects. However, the working mechanisms of DBS in
Externí odkaz:
https://doaj.org/article/279f6f9240164329b9efdc7e1b90af85
Autor:
S E, Cohen, J B, Zantvoord, B N, Wezenberg, J G, Daams, C L H, Bockting, D, Denys, G A, van Wingen
Publikováno v:
Journal of Affective Disorders. 321:201-207
Background: Patients suffering from major depressive disorder (MDD) regularly experience non-response to treatment for their depressive episode. Personalized clinical decision making could shorten depressive episodes and reduce patient suffering. Alt
Autor:
G A, van Wingen
Publikováno v:
Tijdschrift voor psychiatrie. 62(10)
Publikováno v:
Neuroscience, 191, pp. 38-45
Neuroscience, 191, 38-45
Neuroscience, 191, 38-45
Gonadal hormones are known to influence the regulation of emotional responses and affective states. Whereas fluctuations in progesterone and estradiol are associated with increased vulnerability for mood disorders, testosterone is mainly associated w
Autor:
G. A. van Wingen, Jan K. Buitelaar, Guillén Fernández, Robbert J. Verkes, F. van Broekhoven, Torbjörn Bäckström, Karl Magnus Petersson
Publikováno v:
Molecular Psychiatry, 13, pp. 325-333
Molecular Psychiatry
Molecular psychiatry, 13(3), 325-333. Nature Publishing Group
Molecular Psychiatry, 13, 325-33
Molecular Psychiatry, 13, 325-333
Molecular Psychiatry, 13, 3, pp. 325-33
Molecular Psychiatry
Molecular psychiatry, 13(3), 325-333. Nature Publishing Group
Molecular Psychiatry, 13, 325-33
Molecular Psychiatry, 13, 325-333
Molecular Psychiatry, 13, 3, pp. 325-33
Contains fulltext : 71365.pdf (Publisher’s version ) (Closed access) The acute neural effects of progesterone are mediated by its neuroactive metabolites allopregnanolone and pregnanolone. These neurosteroids potentiate the inhibitory actions of ga