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2. SIRT5 rs12216101 T>G variant is associated with oxidative stress and mitochondrial dysfunction in patients with non-alcoholic fatty liver disease

3. Hepatocyte depletion of ERK5 impairs the response to lipotoxic oxidative stress resulting in defective insulin receptor signaling

4. Programmed cell death 1 genetic variant and liver damage in nonalcoholic fatty liver disease

5. OC.08.1 PROGRAMMED CELL DEATH 1 GENETIC VARIANT AND LIVER DAMAGE IN NONALCOHOLIC FATTY LIVER DISEASE

6. OC-06A cholestatic pattern predicts liver-related events in patients with nonalcoholic fatty liver disease

9. Neurotensin up-regulation is associated with advanced fibrosis and hepatocellular carcinoma in patients with MAFLD

12. SIRT5 rs12216101 T>G variant is associated with fibrosis severity in patients with non-alcoholic fatty liver disease

13. NR1H4 rs35724 G>C variant modulates liver damage in nonalcoholic fatty liver disease

16. T04.01.11 PREVALENCE OF NAFLD (NON ALCOHOLIC FATTY LIVER DISEASE) IN INFLAMMATORY BOWEL DISEASE: THE IMPACT OF TRADITIONAL RISK FACTORS, INTESTINAL INFLAMMATION AND GENETIC PHENOTYPE

17. PCSK9 rs11591147 R46L loss-of-function variant protects against liver damage in individuals with non-alcoholic fatty liver

21. Causal relationship of hepatic fat with liver damage and insulin resistance in nonalcoholic fatty liver

24. FXR rs35724 G>C variant modulates cholesterol levels, carotid atherosclerosis and liver damage in non-alcoholic fatty liver

25. AA genotype of deSNP rs6726639 of MERTK gene is associated with development of Hepatocellular Carcinoma after eradication of Hepatitis C Virus infection

28. Changes in 13C-aminopyrine breath test predict liver-related events and death in patients with HCV-related previous decompensated child A5 or child A6 to B cirrhosis who achieve SVR after DAA therapy

29. Serum coding and non-coding RNAs as biomarkers of NAFLD and fibrosis severity

30. NS5A gene analysis by next generation sequencing in HCV nosocomial transmission clusters of HCV genotype 1b infected patients

31. Protein phosphatase 1 regulatory subunit 3B gene variation protects against hepatic fat accumulation and fibrosis in individuals at high risk of nonalcoholic fatty liver disease

34. Causal relationship of hepatic fat with liver damage and insulin resistance in nonalcoholic fatty liver

35. TM6SF2gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease

38. Liver follicular helper T-cells in chronic hepatitis C

39. Superficial venous thrombosis: role of inherited deficiency of natural anticoagulants in extension to deep veins

48. IL28B genotype, differential expression of intrahepatis interferon-stimulated genes and response to PEG-IFN and ribavirin therapy in an Italian prospective cohort of genotype 1 hepatitis C patients in 'real life'

49. P0760 : PNPLA3 rs738409 I748M is associated with steatohepatitis in non obese subjects with hepatitis C

50. PNPLA3 RS738409 I748M is associated with steatohepatitis in non obese subjects with hepatitis C

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