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75 results on '"Ambrosetto G."'

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1. The Prognostic Roles of Gender and O6-Methylguanine-DNA Methyltransferase Methylation Status in Glioblastoma Patients: The Female Power

2. Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy

4. Correction to: Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study

5. Erratum to: Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy

6. High dose intravenous immune globulins and plasma exchange in Guillain-Barré Syndrome

8. Correction to: Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study (Journal of Neuro-Oncology, (2016), 128, 1, (157-162), 10.1007/s11060-016-2093-1)

9. Which elderly newly diagnosed glioblastoma patients can benefit from radiotherapy and temozolomide? A PERNO prospective study

10. Erratum to: Survival prediction in high-grade gliomas using CT perfusion imaging [J Neurooncol (2015) 123, 93-102, DOI 10.1007/s11060-015-1766-5]

11. Erratum to: Incidence of neuroepithelial primary brain tumors among adult population of Emilia-Romagna Region, Italy

12. Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I-III

14. Definition of miRNAs Expression Profile in Glioblastoma Samples: The Relevance of Non-Neoplastic Brain Reference

15. A prospective study on the incidence and prognosis of Guillain-Barre syndrome in Emilia-Romagna region, Italy (1992-1993)

20. "Painful legs and moving toes" associated with polyneuropathy.

24. Familial amyloid polyneuropathy: report of a family

28. Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?

31. The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance.

32. The syndrome of polymicrogyria, thalamic hypoplasia, and epilepsy with CSWS.

33. Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?

34. Paroxysmal bipedal activity during syncope related to carotid body tumor.

35. Sleep-related hypermotor seizures in aspartylglucosaminuria: a case report.

36. Variation in lamotrigine plasma concentrations with hormonal contraceptive monthly cycles in patients with epilepsy.

37. Late-onset PANDAS syndrome with abdominal muscle involvement.

38. Ictal and nonictal paroxysmal events in infantile neuroaxonal dystrophy: polygraphic study of a case.

39. Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE)

40. Treatable partial epilepsy and unilateral opercular neuronal migration disorder.

41. Unilateral opercular macrogyria and benign childhood epilepsy with centrotemporal (rolandic) spikes: report of a case.

42. Occipital lobe seizures related to clinically asymptomatic celiac disease in adulthood.

43. Antiepileptic drug treatment of benign childhood epilepsy with rolandic spikes: is it necessary?

44. Orthostatic tremor: essential and symptomatic cases.

45. Hyperammonemia in asterixis induced by carbamazepine: two case reports.

46. Familial amyloid polyneuropathy: report of a family.

47. Drop attacks: an ominous change in the evolution of partial epilepsy.

49. Marfan's syndrome, recurrent complex partial status epilepticus and myoclonus: a case report.

50. Predictive factors of seizure frequency and duration of antiepileptic treatment in rolandic epilepsy: a retrospective study.

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