Suchergebnisse - "Brooks, William"

PubPharm (15)

1

Biomarker clustering in autosomal dominant Alzheimer's disease

enthalten in: Alzheimer's & dementia : the journal of the Alzheimer's Association | 2023

von Luckett, P. | Chen, C. | Gordon, B. | +41

2

Association of BDNF Val66Met With Tau Hyperphosphorylation and Cognition in Dominantly Inherited Alzheimer Disease

enthalten in: JAMA neurology | 2022

von Lim, Y. | Maruff, P. | Barthélemy, N. | +118

ErratumIn: JAMA Neurol. 2022 Mar 1;79(3):313. - PMID 35285879

3

Higher CSF sTNFR1-related proteins associate with better prognosis in very early Alzheimer's disease

enthalten in: Nature communications | 2021

von Hu, W. | Ozturk, T. | Kollhoff, A. | +103

4

Amyloid and Tau Pathology Associations With Personality Traits, Neuropsychiatric Symptoms, and Cognitive Lifestyle in the Preclinical Phases of Sporadic and Autosomal Dominant Alzheimer's Disease

enthalten in: Biological psychiatry | 2021

von Pichet Binette, A. | Vachon-Presseau, �. | Morris, J. | +108

5

A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer's disease

enthalten in: Nature medicine | 2020

von Barthélemy, N. | Li, Y. | Joseph-Mathurin, N. | +118

6

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

enthalten in: Nature medicine | 2019

von Swarup, V. | Hinz, F. | Rexach, J. | +116

7

Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2 : genetic, clinical and neuropathological analysis

enthalten in: Acta neuropathologica | 2013

von Dobson-Stone, C. | Luty, A. | Thompson, E. | +12

8

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology : genetic linkage to chromosome 9

enthalten in: BMC neurology | 2008

von Luty, A. | Kwok, J. | Thompson, E. | +9

9

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation : an international initiative

enthalten in: The Lancet. Neurology | 2007

von Rademakers, R. | Baker, M. | Gass, J. | +47

ErratumIn: Lancet Neurol. 2007 Dec;6(12):1037

10

Mutations in progranulin explain atypical phenotypes with variants in MAPT

enthalten in: Brain : a journal of neurology | 2006

von Pickering-Brown, S. | Baker, M. | Gass, J. | +11

CommentIn: Brain. 2006 Nov;129(Pt 11):2808-10. - PMID 17071919