Effects of contextual processing on visual conditional associative learning in schizophrenia

Biological Psychiatry

Volumn 48, Issue 5, 2000, Pages 406-414

  Gold, James M ^a   Bish, Joel A ^a   Iannone, Virginia N ^a   Hobart, Mary P ^a   Queern, Caleb A ^a   Buchanan, Robert W ^a  

^a MARYLAND PSYCHIATRIC RESEARCH CENTER   (United States)

Author keywords

Conditional associative learning; Context; Memory; Schizophrenia

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEEDBACK SYSTEM; HUMAN; INFORMATION PROCESSING; LEARNING; MEMORY; PRIORITY JOURNAL; SCHIZOPHRENIA; STATE DEPENDENT LEARNING;

ADULT; ASSOCIATION LEARNING; BIOFEEDBACK (PSYCHOLOGY); COGNITION; FEMALE; HUMANS; MALE; MENTAL RECALL; MODELS, PSYCHOLOGICAL; PSYCHIATRIC STATUS RATING SCALES; SCHIZOPHRENIC PSYCHOLOGY; VISUAL PERCEPTION;

EID: 0034282831     PISSN: 00063223     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-3223(00)00930-6     Document Type: Article

References (18)

1. Baddeley A., Wilson B.A. When implicit learning fails Amnesia and the problem of error elimination. Neuropsychologia. 2:1994;53-68.
2. Braver T.S., Barch D.M., Cohen J.D. Cognition and control in schizophrenia A computational model of dopamine and prefrontal function. Biol Psychiatry. 46:1999;312-328.
3. Cohen J.D., Barch D.M., Carter C., Servan-Schreiber D. Context-processing deficits in schizophrenia Converging evidence from three theoretically motivated cognitive tasks. J Abnorm Psychol. 108:1999;120-133.
4. Cohen J.D., Servan-Schreiber D. Context, cortex, and dopamine A connectionist approach to behavior and biology in schizophrenia. Psychol Rev. 99:1992;45-77.
5. Kemali D., Maj M., Gladerisi S., Monteleone P., Mucci A. Conditional associative learning in drug-free schizophrenia patients. Neuropsychobiology. 17:1987;30-34.
6. Levine B., Stuss D.T., Milberg W.P. Effects of aging on conditional associative learning Process analyses and comparison with focal frontal lesions. Neuropsychology. 11:1997;367-381.
7. Liang K.Y., Zeger S. Longitudinal data analysis using generalized linear models. Biometrika. 73:1985;13-22.
8. O’Carroll R.E., Russell H.H., Lawrie S.M., Johnstone E.C. Errorless learning and the cognitive rehabilitation of memory-impaired schizophrenia patients. Psychol Med. 29:1999;105-112.
9. Petrides M. Deficits in non-spatial conditional associative learning after periarcuate lesions in the monkey. Behav Brain Res. 16:1985;95-101.
10. Petrides M. Deficits on conditional associative-learning tasks after frontal and temporal lobe lesions in man. Neuropsychologia. 23:1985;601-614.
11. Petrides M. Motor conditional associative learning after selective prefrontal lesions in the monkey. Behav Brain Res. 5:1982;407-413.
12. Petrides M. Nonspatial conditional learning impaired in patients with unilateral frontal but not unilateral temporal lobe excisions. Neuropsychologia. 28:1990;137-149.
13. Petrides M. Visuo-motor conditional associative learning after frontal and temporal lobe lesions in the human brain. Neuropsychologia. 35:1997;989-997.
14. Petrides M., Alivisatos B., Evans A.C., Meyer E. Dissociation of human mid-dorsolateral from posterior dorsolateral frontal cortex in memory processing. Proc Natl Acad Sci U S A. 90:1993;873-877.
15. Rushe T.M., Woodruff P.W.R., Murray R.M., Morris R.G. Episodic memory and learning in patients with chronic schizophrenia. Schizophr Res. 35:1999;85-96.
16. Servan-Schreiber D., Cohen J.D., Steingard S. Schizophrenia deficits in the processing of context. A test of a theoretical model. Arch Gen Psychiatry. 53:1996;1105-1112.
17. Slamecka N.J., Graf P. The generation effect Delineation of a phenomenon. J Exp Psychol Learn Mem Cogn. 4:1978;592-604.
18. Wilkinson G.S. The Wide Range Achievement Test 3, Administration Manual. 1993;Wide Range, Wilmington, DE.