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1. Phenotype and imaging features associated with APP duplications

2. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

3. Comparison of Pittsburgh compound B and florbetapir in cross‐sectional and longitudinal studies

4. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

5. Primary brain calcification: an international study reporting novel variants and associated phenotypes.

6. Analysis of shared heritability in common disorders of the brain

7. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

8. Analysis of shared heritability in common disorders of the brain.

9. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.

10. Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers

11. A trial of gantenerumab or solanezumab in dominantly inherited Alzheimer’s disease

13. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.

14. Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease

15. Frontotemporal dementia and its subtypes: a genome-wide association study

16. Plasma amyloid levels within the Alzheimer's process and correlations with central biomarkers

17. Added value of 18F-florbetaben amyloid PET in the diagnostic workup of most complex patients with dementia in France: A naturalistic study

18. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

20. Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experience

23. Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers

24. Early Cognitive, Structural, and Microstructural Changes in Presymptomatic C9orf72 Carriers Younger Than 40 Years

25. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

28. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

29. Exploring Links Between Psychosis and Frontotemporal Dementia Using Multimodal Machine Learning: Dementia Praecox Revisited

32. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

35. Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

36. Effect of the Histone Deacetylase Inhibitor FRM-0334 on Progranulin Levels in Patients With Progranulin Gene Haploinsufficiency

37. Clinical and genetic characteristics of late-onset Huntington's disease

38. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

40. Adult-onset genetic leukoencephalopathies: A MRI pattern-based approach in a comprehensive study of 154 patients

43. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

45. Frontal Assessment Battery is a marker of dorsolateral and medial frontal functions: A SPECT study in frontotemporal dementia

46. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

48. PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum

49. Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings

50. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

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