Rezultaty - Neill R. Graff‐Radford
- Rezultaty 1 - 20 Rezultaty od 231
- Idź do następnej strony
-
1
-
2
-
3
Alzheimer Disease od Richard J. Caselli, Thomas G. Beach, David S. Knopman, Neill R. Graff‐Radford
Wydane 2017Revisão -
4
-
5
-
6
-
7
-
8
-
9
-
10
-
11
Computerized Analysis of Speech and Language to Identify Psycholinguistic Correlates of Frontotemporal Lobar Degeneration od Serguei Pakhomov, Glenn E. Smith, Dustin Alfonso Chacón, Yara Feliciano, Neill R. Graff‐Radford, Richard J. Caselli, David S. Knopman
Wydane 2010Artigo -
12
Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains od Li Ma, Mariet Allen, Nobutaka Sakae, Nilüfer Ertekin‐Taner, Neill R. Graff‐Radford, Dennis W. Dickson, Steven G. Younkin, Daniel Sevlever
Wydane 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 od Tanis J. Ferman, Zoe Arvanitakis, Hiroshige Fujishiro, Ranjan Duara, Francine Parfitt, M. Purdy, Carol Waters, Warren Barker, Neill R. Graff‐Radford, Dennis W. Dickson
Wydane 2012Artigo -
17
Genetic variants in a haplotype block spanningIDE are significantly associated with plasma A?42 levels and risk for Alzheimer disease od Nil�fer Ertekin-Taner, Mariet Allen, Daniel J. Fadale, Leah Scanlin, Linda H. Younkin, Ronald C. Petersen, Neill R. Graff‐Radford, Steven G. Younkin
Wydane 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 od Jan Malm, Neill R. Graff‐Radford, Masatsune Ishikawa, Bjarne Winther Kristensen, Ville Leinonen, Etsuro Mori, Brian Owler, Mats Tullberg, Michael A. Williams, Norman Relkin
Wydane 2013Artigo -
19
APOE ε4/ε4 diminishes neurotrophic function of human iPSC-derived astrocytes od Jing Zhao, Mary Dabney Davis, Yuka A. Martens, Mitsuru Shinohara, Neill R. Graff‐Radford, Steven G. Younkin, Zbigniew K. Wszołek, Takahisa Kanekiyo, Guojun Bu
Wydane 2017Artigo -
20
<i>Fus</i> gene mutations in familial and sporadic amyotrophic lateral sclerosis od 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
Wydane 2010Artigo
Narzędzie wyszukiwania:
Podobne hasła
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