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2. Genome wide association study of clinical duration and age at onset of sporadic CJD

3. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (Nature Communications, (2021), 12, 1, (3417), 10.1038/s41467-021-22491-8)

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

5. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores (Nature Communications, (2021), 12, 1, (3417), 10.1038/s41467-021-22491-8)

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

8. 20769. IDENTIFICACIÓN DE UNA MUTACIÓN PATOGÉNICA EN ARPP21 EN PACIENTES CON ESCLEROSIS LATERAL AMIOTRÓFICA

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

12. Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study

13. Concordance of cerebrospinal fluid real-time quaking-induced conversion across the European Creutzfeldt-Jakob Disease Surveillance Network

14. Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.

15. Tau deposition patterns are associated with functional connectivity in primary tauopathies

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

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

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

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

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

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

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

36. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

37. SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

38. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

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

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

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