Resultados de procura - Neill R. Graff‐Radford
- Mostrando 1 - 20 Resultados de 231
- Go to Next Page
-
1
-
2
-
3
Alzheimer Disease por Richard J. Caselli, Thomas G. Beach, David S. Knopman, Neill R. Graff‐Radford
Publicado 2017Revisão -
4
-
5
-
6
-
7
-
8
-
9
Hippocampal Sclerosis in the Elderly por Winnie Pao, Dennis W. Dickson, Julia E. Crook, NiCole A. Finch, Rosa Rademakers, Neill R. Graff‐Radford
Publicado 2011Artigo -
10
-
11
Computerized Analysis of Speech and Language to Identify Psycholinguistic Correlates of Frontotemporal Lobar Degeneration por Serguei Pakhomov, Glenn E. Smith, Dustin Alfonso Chacón, Yara Feliciano, Neill R. Graff‐Radford, Richard J. Caselli, David S. Knopman
Publicado 2010Artigo -
12
Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains por Li Ma, Mariet Allen, Nobutaka Sakae, Nilüfer Ertekin‐Taner, Neill R. Graff‐Radford, Dennis W. Dickson, Steven G. Younkin, Daniel Sevlever
Publicado 2016Artigo -
13
-
14
-
15
-
16
Pathology and temporal onset of visual hallucinations, misperceptions and family misidentification distinguishes dementia with Lewy bodies from Alzheimer's disease por Tanis J. Ferman, Zoe Arvanitakis, Hiroshige Fujishiro, Ranjan Duara, Francine Parfitt, M. Purdy, Carol Waters, Warren Barker, Neill R. Graff‐Radford, Dennis W. Dickson
Publicado 2012Artigo -
17
Genetic variants in a haplotype block spanningIDE are significantly associated with plasma A?42 levels and risk for Alzheimer disease por Nil�fer Ertekin-Taner, Mariet Allen, Daniel J. Fadale, Leah Scanlin, Linda H. Younkin, Ronald C. Petersen, Neill R. Graff‐Radford, Steven G. Younkin
Publicado 2004Artigo -
18
Influence of comorbidities in idiopathic normal pressure hydrocephalus — research and clinical care. A report of the ISHCSF task force on comorbidities in INPH por Jan Malm, Neill R. Graff‐Radford, Masatsune Ishikawa, Bjarne Winther Kristensen, Ville Leinonen, Etsuro Mori, Brian Owler, Mats Tullberg, Michael A. Williams, Norman Relkin
Publicado 2013Artigo -
19
-
20
<i>Fus</i> gene mutations in familial and sporadic amyotrophic lateral sclerosis por Rosa Rademakers, Heather Stewart, Mariely DeJesus‐Hernandez, Charles Krieger, Neill R. Graff‐Radford, Marife Fabros, Hannah Briemberg, Neil R. Cashman, Andrew Eisen, Ian R. Mackenzie
Publicado 2010Artigo
Ferramentas de procura:
Materias Relacionadas
Medicine
Disease
Biology
Pathology
Dementia
Genetics
Internal medicine
Gene
Alzheimer's disease
Neuroscience
Psychology
Frontotemporal dementia
Frontotemporal lobar degeneration
Allele
Genotype
Psychiatry
Single-nucleotide polymorphism
C9orf72
Mutation
Atrophy
Oncology
Amyotrophic lateral sclerosis
Genome-wide association study
Apolipoprotein E
Dementia with Lewy bodies
Genetic association
Biomarker
Cognition
Progressive supranuclear palsy
Trinucleotide repeat expansion