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

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

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

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

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

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

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

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

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

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

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

22. Inappropriate prescription of benzodiazepines in acutely hospitalized older patients

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

24. Thrombotic and hemorrhagic complications in idiopathic erythrocytosis

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

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

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

29. HFE mutations in idiopathic erythrocytosis

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

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

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

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

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

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

37. Effect of busulfan on JAK2V617F allele burden

38. How the Real-Life Diagnostic and Therapeutic Approach Changed in the Last Two Decades in the Thrombocythemic Patients with Ph- Negative Myeloproliferative Neoplasm. Report on 2388 Subjects of the Registro Italiano Trombocitemie (RIT)

39. Thrombosis History and Relationship With Low Thrombocytosis, Leukocytosis, and Other Characteristics At Diagnosis In 977 Essential Thrombocythemia Patients A Multivariate Analysis Of The Registro Italiano Trombocitemie (RIT)

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