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1. P156 Muscle biopsy findings in a large cohort of patients affected by valosin containing protein disease: preliminary analysis of the international multicentric VCP study

2. Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease

5. Clinicopathologic correlations in 172 cases of rapid eye movement sleep behavior disorder with or without a coexisting neurologic disorder

7. Neuropathology of a patient with Alzheimer disease treated with low doses of verubecestat

8. Copathology in Progressive Supranuclear Palsy: Does It Matter?

10. Type II beta-amyloid 42 Filaments from Human Brain

15. Does ALS‐FUS without FUS mutation represent ALS‐FET? Report of three cases

16. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

17. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

18. Heterozygous APOE Christchurch in familial Alzheimer's disease without mutations in other Mendelian genes

26. Clinical Conditions 'Suggestive of Progressive Supranuclear Palsy'—Diagnostic Performance

35. How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy

36. Nanoscale structure of amyloid-beta plaques in Alzheimer's disease

37. Leukotriene Generation and Neutrophil Infiltration After Experimental Acute Pancreatitis

38. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt–Jakob disease

42. Hepatic involvement in pancreatitis-induced lung damage

43. Predictors of survival in sporadic Creutzfeldt–Jakob disease and other human transmissible spongiform encephalopathies

47. Nephropathies and exposure to perchloroethylene in dry-cleaners

48. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

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