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1. Pharmacogenetics of antipsychotic therapy: pivotal research issues and the prospects for clinical implementation

2. Genetics of Posttraumatic Stress Disorder

3. Angiotensin converting enzyme gene insertion/deletion polymorphism: Case-control association studies in schizophrenia, major affective disorder, and tardive dyskinesia and a family-based association study in schizophrenia

4. Association between the serotonin 2C receptor gene and tardive dyskinesia in chronic schizophrenia: additive contribution of 5-HT2C ser and DRD3 gly alleles to susceptibility

5. Possible precipitants of psychiatric hospitalization in patients with major depression: Results from the Jerusalem collaborative depression project

6. Support for a Chromosome 18p Locus Conferring Susceptibility to Functional Psychoses in Families with Schizophrenia, by Association and Linkage Analysis

7. An association between clozapine-induced agranulocytosis in schizophrenics and HLA-DQB1*0201

8. 5-HT2C (HTR2C)serotonin receptor gene polymorphism associated with the human personality trait of reward dependence: Interaction with dopamine D4 receptor (D4DR) and dopamine D3 receptor (D3DR) polymorphisms

9. Onset and time course of antidepressant action: psychopharmacological implications of a controlled trial of electroconvulsive therapy

10. Interactive effect of cytochrome P450 17α-hydroxylase and dopamine D3 receptor gene polymorphisms on abnormal involuntary movements in chronic schizophrenia

11. Genetics of unipolar major depressive disorder

12. PFO

13. PRPP Synthetase Superactivity

14. Pyoderma Gangrenosum

15. Poly- and Dermatomyositis

16. Parasternal Chondrodynia

17. Purpura Rheumatica

18. Puna Soroche

19. Primary Systemic Carnitine Deficiency

20. Pancreatitis, Autoimmune

21. Pure Cutaneous Histiocytosis

22. Polyneuropathy, Chronic Inflammatory Demyelinating

23. Persistent Atrioventricular Ostium

24. Primary (Congenital) Intestinal Lymphangiectasia

25. Primary Carnitine Deficiency

26. Primary Sclerosing Cholangitis

27. Pulmonary Hypertension

28. Phosphorylase B Kinase Deficiency

29. Primary Open Angle Glaucoma

30. Pseudohypoaldosteronism Type II

31. Pulmonary Atresia with Ventricular Septal Defect

32. Pharyngoesophageal Diverticula

33. Purpura Schoenlein-Henoch

34. Partial Androgen Insensitivity Syndrome

35. Primary Cutaneous Anaplastic Large-Cell Lymphoma

36. Primary Pulmonary Hypertension

37. Pott’s Disease (Spine)

38. Pelizaeus-Merzbacher Disease

39. Pityriasis Simplex Faciei

40. PME Type 1

41. Papillary Duct Ectasia

42. Porphyria, Variegate

43. Pneumonia, Cryptogenic Organizing

44. Persistent Truncus Arteriosus

45. Pulmonary Valve Insufficiency

46. Pyridoxine Excess

47. Propionyl CoA Carboxylase Deficiency

48. 9p Monosomy

49. PFIC Type 2

50. Polyendocrinopathy Ectodermal Dystrophy, Autoimmune

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