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Your search keyword '"Pierantoni Chiara"' showing total 577 results

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1. Trans-arterial chemo-embolization (TACE), with either lipiodol (traditional TACE) or drug-eluting microspheres (precision TACE, pTACE) in the treatment of hepatocellular carcinoma: efficacy and safety results from a large mono-institutional analysis

2. Epidermal Growth Factor Receptor (EGFR) gene copy number (GCN) correlates with clinical activity of irinotecan-cetuximab in K-RAS wild-type colorectal cancer: a fluorescence in situ (FISH) and chromogenic in situ hybridization (CISH) analysis

5. Factors That Affect Adequacy of Colon Cleansing for Colonoscopy in Hospitalized Patients

10. Irinotecan-Induced Transient Dysarthria: Case Series and Updated Literature Review

17. Role of maspin in cancer

18. Chromoendoscopy is not superior to white light endoscopy in improving adenoma detection in Lynch Syndrome cohort undergoing surveillance with high-resolution colonoscopy: a real-world evidence study

20. Cetuximab plus gemcitabine and cisplatin compared with gemcitabine and cisplatin alone in patients with advanced pancreatic cancer: a randomised, multicentre, phase II trial

21. Chromoendoscopy Is Not Superior to White Light Endoscopy in Improving Adenoma Detection in Lynch Syndrome Cohort Undergoing Surveillance with High-Resolution Colonoscopy: A Real-World Evidence Study.

22. Factors That Affect Adequacy of Colon Cleansing for Colonoscopy in Hospitalized Patients

23. Pancreas Annulare

24. Pulmonary Valve Incompetence

25. Precocious Puberty

26. Protein S Deficiency

27. Proliferative Diabetic Retinopathy

28. Purine Nucleoside Phosphorylase Deficiency

29. Progressive Myoclonus Epilepsy of Unverricht-Lundborg Type

30. Pseudohypoaldosteronism, Autosomal Recessive

31. Pendred Syndrome

32. Protoporphyria, Erythropoietic

33. Premature Complexes, Atrial and Ventricular

34. PHT

35. Porphyria, Variegate

36. Paroxysmal Cold Hemoglobinuria

37. Polychondritis Recidivans

38. Pierre Robin Syndrome

39. Preauricular Cyst

40. Phrenic Nerve Palsy

41. Pancreatitis, Hereditary

42. Palmitoylcarnitine Transferase

43. PFK Deficiency

44. 5p Monosomy

45. Partial Tetrasomy 15(pter-q13)

46. Primary Empty Sella

47. Persistent Neonatal Hyperinsulinism

48. Periodic Vestibulocerebellar Ataxia

49. Pachyonychia Congenita Type I

50. Pterin-4a-Carbinolamine Dehydratase Deficiency

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