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152. Associating Alzheimer’s disease pathology with its cerebrospinal fluid biomarkers

154. De BPSD-DS evaluatieschaal voor dementiegerelateerde gedragsveranderingen bij mensen met downsyndroom (BPSD-DS II): optimalisatie en verdere validatie

157. Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

168. Microtubule associated protein tau p.R406W patient carriers present with a nonconforming clinical phenotype.

170. The Behavioral and Psychological Symptoms of Dementia in Down Syndrome Scale (BPSD-DS II): Optimization and Further Validation

172. Extensive Genetic And Phenotypic Description Of MAPT p.R406W In The Flanders-Belgian Population

187. Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

188. Association study of cholesterol-related genes in Alzheimer’s disease

189. A family‐based genetic study identifies mutations in TLR9 impairing receptor activation

190. Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.

191. Serum and cerebrospinal fluid Neutrophil gelatinase-associated lipocalin (NGAL) levels as biomarkers for the conversion from mild cognitive impairment to Alzheimer's disease dementia

198. Extensive Genetic And Phenotypic Description Of MAPT p.R406W In The Flanders-Belgian Population (4248)

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