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WFSBP 2015
Scientific Programme
|
Wednesday, 17 June 2015
P-19
Poster Presentation
12:45–14:15
Muses Foyer
Basic and Clinical Neuroscience/Treatment Methods
Chair:
Nikolaos Venizelos, Sweden
Co-Chair: Eleytheria Tsalta, Greece
P-19-001
A pilot study in cytogenetic biomarkers and molecular study
of Phospholipase D3 (PLD3) gene in Alzheimer‘s disease
Jayalakshmi Ramalingam, India
A. Meyyazhagan, S. K. Shanmugam, M. Iyer, S. Keshavarao,
B. Vellingiri
P-19-002
Postnatal exposure to moderate noise impaired behavior,
learning and memory in adult female rat
Li-Ho Tseng, Taiwan
C.-Y. Chou, P.-C. Hsu, Y.-J. Ho, J.-F. Hwang, S.-C. Sheen
P-19-003
Role of the neurometabolites in emotional processing
Dominik Denzel, Germany
M. Walter, L. Demenecu, F. von Düring, L. Colic, S. Li
P-19-004
Spontaneous behavior and oxidative stress of male adult
rats exposed to moderate noise
Li-Ho Tseng, Taiwan
P.-C. Hsu, I.-L. Chen, C.-Y. Chou, C.-W. Lee
P-19-005
fMRI reveals abnormalities in neural processing of reward
prediction errors in pathological gambling
Martin Kronbichler, Germany
T. Eigenberger, P. Schwartenbeck, N. Thon, M. Fauth-Bühler,
T. Lemenager, K. Mann, F. M. Wurst
P-19-006
Depressive symptoms and cognitive functioning in coronary
artery disease patients: Effect of triiodothyronine
Julius Burkauskas, Lithuania
J. Brozaitiene, M. Staniute, R. Bunevicius
P-19-007
A pilot study in cytogenetic biomarkers and molecular study
of Phospholipase D3 (PLD3) gene in Alzheimer‘s disease
Alagamuthu Karthick Kumar, India
S. Suresh Kumar, B. Balamurali Krishnan, V. Balachandar,
K. Sasikala
P-19-008
Analysis of chromosomal abnormalities and ube3a gene
mutation in angelman syndrome (as) coimbatore popu-
lation
Padmavathi Viji, India
A. Meyyazhagan, S. Keshavarao, B. Vellingiri
P-19-009
Association between depression and polymorphisms of
the tryptophan hydroxylase (tph) and the 5,10-methylene-
tetrahydrofolate reductase (mthfr) genes in the Tunisian
population
Mohamed Amine Sayadi, Tunisia
O. Achour, M. H. Saadaoui, A. Mhalla, F. Neffati, A. Omez-
zine, W. Douki, A. Bousslama, L. Gaha, F. Najjar, A. Malafosse
P-19-010
Association study of 45 SNPs in Russian patients with
Alzheimer‘s disease
Anna Bocharova, Russia
A. Marusin, N. Zhukova, V. Alifirova, I. Zhukova, V. Stepanov
P-19-011
Epistastatic interaction study between comt, 5-htr2a and
nrg1 gene variants on schizophrenia
Shiau Foon Tee, Malaysia
P. Y. Tang, T. J. Chow
P-19-012
Exome sequencing identifies a novel risk variant in a dopa-
mine regulation gene in familial schizophrenia
Thelma Bittianda Kuttapa, India
J. John, J. Jibin, N. V. L., D. S. N.
P-19-013
Gene expression and psychiatric analysis of 100 Iranian
methamphetamine addicted individuals
Arvin Haghighatfard, Iran
P-19-014
Prevalence of 22q11.2 deletions in a Chilean population
with schizophrenia
Aida Ruiz, Chile
P. John, R. Murray, E. Miranda, P. Sham, F. Benavides, G. Repetto
P-19-015
Automatic classification of first episode psychosis obtained
with gray matter thickness
Paolo Brambilla, Italy
U. Castellani, C. Perlini, V. Marinelli, N. Dusi, M. Bellani,
G. Rambaldelli, A. Lasalvia, M. Ruggeri, L. Squarcina
P-19-016
Basal ganglia imaging (DaTscan): Association with anti
psychotic treatment in elderly patients
Panagiota Fexi, Greece
N. Kokras, C. Siarkos, E. Katritzoglou, D. Pappa, G. Limouris,
A. Politis
P-19-017
Changes in brain volume and cognitive function in middle
adulthood: A framework for investigating neurodegenera-
tion in schizophrenia
Rizwan Ahmed, USA
M. Bellani, G. Rambaldelli, R. White, V. Diwadkar, P. Brambilla