164 results on '"Fiorelli, G"'
Search Results
2. Stroke and Alcohol Intake in a Hospital Population: A Case-Control Study
3. Rosette Inhibition Test And Cell-Mediated Immunity
4. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload
5. Bone and joint involvement in genetic hemochromatosis: role of cirrhosis and iron overload
6. Liver iron influences the response to interferon alpha therapy in chronic hepatitis C
7. Relationship between TNF-alpha and iron metabolism in differentiating human monocytic THP-1 cells
8. Haemochromatosis in patients with b-thalassemia trait
9. No association between genetic hemochromatosis and alpha1-antitrypsin deficiency
10. Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overload
11. Iron stores, response to alpha-interferon therapy, and effects of iron depletion in chronic hepatitis C
12. Liver iron concentration in chronic viral hepatitis: a study of 98 patients
13. Prognostic factors for hepatocellular carcinoma in genetic hemochromatosis
14. HCV-RNA POSITIVE HEPATITIS IN LIVER-TRANSPLANT RECIPIENTS
15. H-ferritin receptors, intracellular H-ferritin and tumor necrosis factor alpha in activated THP-1 myielomonocytic cells
16. Preclinical hypogonadism in genetic hemochromatosis in the early stage of the disease: evidence of hypothalamic dysfunction
17. Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association
18. Liver damage in Italian patients with hereditary hemochromatosis is highly influenced by hepatitis B and C virus infection
19. Hepatitis C virus infection in patients with idiopathic hemochromatosis (IH) and porphyria cutanea tarda (PCT)
20. Prevalence of idiopathic hemochromatosis in Italy: study of 1301 blood donors
21. Cardiac alterations in 36 consecutive patients with idiopathic haemochromatosis: polygraphic and echocardiographic evaluation
22. Linkage analysius of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F
23. SPECIFIC BINDING-SITES FOR H-FERRITIN ON HUMAN-LYMPHOCYTES - MODULATION DURING CELLULAR PROLIFERATION AND POTENTIAL IMPLICATION IN CELL-GROWTH CONTROL
24. Characteristics of the membrane receptor for human H-ferritin
25. Prevalence of idiopathic hemochromatosis in Italy: study of 1301 blood donors
26. The effect of dietary magnesium supplementation on the cellular abnormalities of erythrocytes in patients with beta thalassemia intermedia
27. A survey of adverse events in 11,241 patients with chronic viral hepatitis treated with alfa interferon
28. Dietary magnesium supplementation affects erythrocyte ion transport and composition in patients with beta thalassemia intermedia
29. Malattie Neurologiche
30. Binding and bioeffects of Ipriflavone on a human preosteoclastic cell line. S
31. Haemochromatosis in patients with beta-thalassaemia trait
32. High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda
33. Nontransfusional Iron Overload in Thalassemia Intermedia: Role of the Hemochromatosis Allele
34. Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis
35. Iron in the pathogenesis of hepatocellular carcinoma
36. Heterogeneity of binding sites of estrogens and proliferative effect of estrogenic molecules in human colon cancer cell lines
37. Erythrocyte ferritin in patients on chronic hemodialysis treatment
38. Iron metabolism in thalassemia intermedia
39. Epidermal growth factor, epidermal growth factor receptor, and transforming growth factor-alpha in human hyperplastic prostate tissue: expression and cellular localization.
40. Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean
41. Role of hemichrome binding to erythrocyte membrane in the generation of band-3 alterations in beta-thalassemia intermedia erythrocytes
42. Genetic interactions in thalassemia intermedia: Analysis of β‐Mutations, α‐Genotype, γ‐Promoters, and β‐LCR hypersensitive sites 2 and 4 in Italian patients
43. Different origin of nt 1246 glucose-6-phosphate dehydrogenase mutation [letter; comment]
44. Effect of estrogens and progesterone on human peripheral erythroid burst‐forming unit (BFU‐E) growth
45. Specific binding sites for H-ferritin on human lymphocytes: modulation during cellular proliferation and potential implication in cell growth control
46. Association of hereditary spherocytosis and idiopathic hemochromatosis. A synergistic effect in determining iron overload
47. The iron status of Italian subjects with beta-thalassemia trait
48. Iron overload in subjects with beta-thalassaemia trait: role of idiopathic haemochromatosis gene
49. Impiego di un'associazione contenente i coenzimi delle vitamine B1, B6 e B12 nella terapia di supporto dell'epatopatia alcoolica. [Use of a combination containing the coenzymes of vitamins B1, B6 and B12 in support therapy of alcoholic hepatopathy]
50. Immunohistochemical evaluation of a panel of monoclonal antibodies for the diagnosis of small cell lung cancer
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