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47 results on '"Girelli D."'

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1. Clinical factors associated with death in 3044 COVID-19 patients managed in internal medicine wards in Italy: results from the SIMI-COVID-19 study of the Italian Society of Internal Medicine (SIMI)

2. Underdiagnosis and undertreatment of osteoporotic patients admitted in internal medicine wards in Italy between 2010 and 2016 (the REPOSI Register)

3. The multifaceted spectrum of liver cirrhosis in older hospitalised patients: Analysis of the REPOSI registry

4. Prognostic value of degree and types of anaemia on clinical outcomes for hospitalised older patients

5. Disability, and not diabetes, is a strong predictor of mortality in oldest old patients hospitalized with pneumonia

6. CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients

7. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

8. Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders

9. Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery disease

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

11. What changed in the Italian internal medicine and geriatric wards during the lockdown

12. Pain and Frailty in Hospitalized Older Adults

13. Pattern of comorbidities and 1-year mortality in elderly patients with COPD hospitalized in internal medicine wards: data from the RePoSI Registry

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

15. Choice and Outcomes of Rate Control versus Rhythm Control in Elderly Patients with Atrial Fibrillation: A Report from the REPOSI Study

16. Defining aging phenotypes and related outcomes: Clues to recognize frailty in hospitalized older patients

17. Pattern of in-hospital changes in drug use in the older people from 2010 to 2016

18. Adherence to antithrombotic therapy guidelines improves mortality among elderly patients with atrial fibrillation: insights from the REPOSI study

19. Genetic studies of body mass index yield new insights for obesity biology

20. rs629301 CELSR2 polymorphism confers a ten-year equivalent risk of critical stenosis assessed by coronary angiography

21. Measurement of urinary hepcidin levels by SELDI-TOF-MS in HFE-hemochromatosis

22. Oxidative stress biomarkers in Fabry disease: is there a room for them?

23. A Five-Step Vascular Ultrasound Examination in Heart Failure: The First Two Years of the 'ABCDE' G-SIUMB Multicenter Study 2018-2022

24. MOLECULAR CHARACTERIZATION OF PATIENTS WITH AND WITHOUT CORONARY ARTERY DISEASE WITH 'EXTREME LDL-C PHENOTYPES'

25. Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype

26. A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia

27. Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations

28. Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA)

29. Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis

30. Frequency and Indications of Parenteral Nutrition in an Acute Palliative Care Unit

31. An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis

32. Correction: Increased Serum Hepcidin Levels in Subjects with the Metabolic Syndrome: A Population Study

33. Correction: Increased Serum Hepcidin Levels in Subjects with the Metabolic Syndrome: A Population Study

34. The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis

35. A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis

36. Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients

37. Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutations

38. Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele

39. Sleep disorders in advanced cancer patients: prevalence and factors associated

40. Interaction of antibodies against cytomegalovirus with heat-shock protein 60 in pathogenesis of atherosclerosis

41. Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

42. Heterogeneity of hemochromatosis in Italy

43. The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients

44. Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F

45. Hepcidin modulation in human diseases: From research to clinic

46. Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies

47. Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms

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