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2. COEXISTENCE OF MULTIPLE GENE VARIANTS IN SOME PATIENTS WITH ERYTHROCYTOSES

4. Peculiar, poorly known, rare congenital bleeding disorders presenting thrombotic events: an understudied chapter of molecular, blood coagulation defects

7. Systemic Mastocytosis and Essential Thrombocythemia: Case Report and Literature Overview

9. Antihypertensive treatment changes and related clinical outcomes in older hospitalized patients

10. Clinical features and outcomes of elderly hospitalised patients with chronic obstructive pulmonary disease, heart failure or both

11. Hyperglycemia at admission, comorbidities, and in-hospital mortality in elderly patients hospitalized in internal medicine wards: data from the RePoSI Registry

12. Peculiar, poorly known, rare congenital bleeding disorders presenting thrombotic events: an understudied chapter of molecular, blood coagulation defects

13. Thrombotic Events in Homozygotes with a Proven or Highly Probable Arg304Gln Factor VII Mutation (FVII Padua)1): Only Limited Replacement Therapy is Needed in Case of Surgery

14. Prevalence and Causes of Anemia in Hospitalized Patients: Impact on Diseases Outcome

17. Increased Prevalence of Reported Cases of Congenital Prekallikrein Deficiency Among African Americans as Compared With the General Population of the United States

18. Vitamin K-Dependent Coagulation Factors That May be Responsible for Both Bleeding and Thrombosis (FII, FVII, and FIX)

19. Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study

20. A structure–function analysis in patients with prekallikrein deficiency

21. New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice

22. African and African-American Contribution to the Knowledge of the FVII Padua (Arg304Gln) Defect

23. Prevalence of use and appropriateness of antidepressants prescription in acutely hospitalized elderly patients

24. Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations

25. Use and prescription appropriateness of drugs for peptic ulcer and gastrooesophageal reflux disease in hospitalized older people

26. The Dysprothrombinemias due to Arg596 Mutations: A Conundrum With No Bleeding Tendency and Venous Thrombosis due to Antithrombin Resistance

27. Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period

29. Inappropriate prescription of benzodiazepines in acutely hospitalized older patients

30. Hospital Care of Older Patients With COPD: Adherence to International Guidelines for Use of Inhaled Bronchodilators and Corticosteroids

31. Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term study

32. Pulmonary embolism in congenital bleeding disorders

33. Thrombotic and hemorrhagic complications in idiopathic erythrocytosis

34. Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed

35. Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis

37. Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders

38. Heparin, coumarin, protein C, antithrombin, fibrinolysis and other clotting related resistances: old and new concepts in blood coagulation

40. HFE mutations in idiopathic erythrocytosis

41. Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period*

42. Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders

43. Factor X Friuli Coagulation Disorder: Almost 50 Years Later

44. Systemic Mastocytosis and Essential Thrombocythemia: Case Report and Literature Overview

45. Prethrombotic, prothrombotic, thrombophilic states, hypercoagulable state, thrombophilia etc.: semantics should be respected even in medical papers

46. Drug-Induced Thrombophilic or Prothrombotic States: An Underestimated Clinical Problem That Involves Both Legal and Illegal Compounds

47. Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years)

48. Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions

49. Unravelling Genetic Mechanisms of Erythrocytosis: A Real-Life Experience from a Single Center

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