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14. Effect of Fluvoxamine on Amyloid-β Peptide Generation and Memory

15. Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies

16. CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.

19. IsCHCHD10Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?: Figure 1

20. Effect of Fluvoxamine on Amyloid-β Peptide Generation and Memory.

21. DNA methylation of theMAPTgene in Parkinson's disease cohorts and modulation by vitamin EIn Vitro

22. C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients

23. Endogenous progesterone levels and frontotemporal dementia: modulation of TDP-43 and Tau levels in vitro and treatment of the A315T TARDBP mouse model

24. P1-285: Sigma non-opioid intracellular receptor 1 and neurodegeneration: prevalence of mutations and therapeutic implications

26. Glycogen synthase kinase-3β and tau genes interact in Alzheimer's disease

33. Variable phenotype of Alzheimer's disease with spastic paraparesis

37. Two novel presenilin-1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimerʼs disease

38. Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22

39. Two novel (M233T and ρ278T) presenilin-1 mutations in early-onset Alzheimerʼs disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype

40. Effect of PSEN1 mutations on MAPT methylation in early-onset Alzheimer’s disease

41. C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients.

44. Rapid and automated quantification of TDP‐43 and FUS mislocalisation for screening of frontotemporal dementia and amyotrophic lateral sclerosis gene variants.

45. C9ORF72repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts

46. GSK3Bpolymorphisms alter transcription and splicing in Parkinson's disease

48. Two novel M233T and ρ278T presenilin1 mutations in earlyonset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin1 mutations with a novel phenotype

49. Two novel presenilin1 mutations Ser169Leu and Pro436Gln associated with very early onset Alzheimer's disease

50. No association of spastic paraparesis genes in PSEN1Alzheimer's disease with spastic paraparesis

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