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1. First-Episode Psychosis Patients Who Deteriorated in the Premorbid Period Do Not Have Higher Polygenic Risk Scores Than Others: A Cluster Analysis of EU-GEI Data

2. Cannabis use as a potential mediator between childhood adversity and first-episode psychosis: results from the EU-GEI case-control study

4. Cognitive functioning throughout adulthood and illness stages in individuals with psychotic disorders and their unaffected siblings

5. Pre-training inter-rater reliability of clinical instruments in an international psychosis research project

6. T regulatory cells as a potential therapeutic target in psychosis? Current challenges and future perspectives.

7. Anxiolytic and panicolytic effects of escitalopram in the elevated T-maze

8. Daily use of high-potency cannabis is associated with more positive symptoms in first-episode psychosis patients: The EU-GEI case-control study

9. Schizophrenia polygenic risk score and cannabis use modify psychosis expression in first episode psychosis patients and population controls

10. The independent and combined influence of schizophrenia polygenic risk score and heavy cannabis use on risk for psychotic disorder: A case-control analysis from the EUGEI study

11. Treated Incidence of Psychotic Disorders in the Multinational EU-GEI Study

14. Comparability between telephone and face-to-face structured clinical interview for DSM-IV in assessing social anxiety disorder.

16. Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

17. Cannabis use and cognitive biases in people with first-episode psychosis and their siblings.

18. The effect of polygenic risk score and childhood adversity on transdiagnostic symptom dimensions at first-episode psychosis: evidence for an affective pathway to psychosis.

19. Methylomic signature of current cannabis use in two first-episode psychosis cohorts.

20. Mental disorders in adults from Ribeirão Preto, Brazil: a cross-sectional analysis of two birth cohorts.

21. The Role of Social Deprivation and Cannabis Use in Explaining Variation in the Incidence of Psychotic Disorders: Findings From the EU-GEI Study.

22. Disengagement from the Ribeirão Preto early intervention program for psychosis: A retrospective cohort study.

23. Self-reported suicidal ideation among individuals with first episode psychosis and healthy controls: Findings from the international multicentre EU-GEI study.

24. Transdiagnostic dimensions of symptoms and experiences associated with immune proteins in the continuity of psychosis.

25. Neurocognition and brain functional connectivity in a non-clinical population-based sample with psychotic experiences.

26. Cannabis use as a potential mediator between childhood adversity and first-episode psychosis: results from the EU-GEI case-control study.

27. The association between reasons for first using cannabis, later pattern of use, and risk of first-episode psychosis: the EU-GEI case-control study.

28. Low doses of fluoxetine for the treatment of emotional premenstrual syndrome: a randomized double-blind, placebo-controlled, pilot study.

29. The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case-control study.

30. Child maltreatment, migration and risk of first-episode psychosis: results from the multinational EU-GEI study.

31. Differences in Patterns of Stimulant Use and Their Impact on First-Episode Psychosis Incidence: An Analysis of the EUGEI Study.

32. Exploring the mediation of DNA methylation across the epigenome between childhood adversity and First Episode of Psychosis-findings from the EU-GEI study.

33. Colchicine reduces the activation of NLRP3 inflammasome in COVID-19 patients.

34. Lifetime cannabis use and childhood trauma associated with CNR1 genetic variants increase the risk of psychosis: findings from the STREAM study.

35. Synergistic effects of childhood adversity and polygenic risk in first-episode psychosis: the EU-GEI study.

36. Development and Validation of Predictive Model for a Diagnosis of First Episode Psychosis Using the Multinational EU-GEI Case-control Study and Modern Statistical Learning Methods.

37. Excess mortality in a cohort of Brazilian patients with a median follow-up of 11 years after the first psychiatric hospital admission.

38. First-Episode Psychosis Patients Who Deteriorated in the Premorbid Period Do Not Have Higher Polygenic Risk Scores Than Others: A Cluster Analysis of EU-GEI Data.

39. Increased blood neutrophil extracellular traps (NETs) associated with early life stress: translational findings in recent-onset schizophrenia and rodent model.

40. Preterm birth and postpartum depression within 6 months after childbirth in a Brazilian cohort.

41. Migration history and risk of psychosis: results from the multinational EU-GEI study.

42. Genetic and psychosocial stressors have independent effects on the level of subclinical psychosis: findings from the multinational EU-GEI study.

43. Validation of the Brazilian version of the Hinting Task and Facial Emotion Recognition Test (FERT-100) in patients with schizophrenia.

44. Early intervention in psychosis in emerging countries: Findings from a first-episode psychosis programme in the Ribeirão Preto catchment area, southeastern Brazil.

45. Childhood Maltreatment, Educational Attainment, and IQ: Findings From a Multicentric Case-control Study of First-episode Psychosis (EU-GEI).

46. Early Schizophrenia and Bipolar Disorder Patients Display Reduced Neural Prepulse Inhibition.

47. Family environment and depressive episode are associated with relapse after first-episode psychosis.

49. Duration of Untreated Psychosis in First-Episode Psychosis is not Associated With Common Genetic Variants for Major Psychiatric Conditions: Results From the Multi-Center EU-GEI Study.

50. The Independent Effects of Psychosocial Stressors on Subclinical Psychosis: Findings From the Multinational EU-GEI Study.

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