Bilaketaren emaitzak - Neill R. Graff‐Radford
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Alzheimer CSF biomarkers may be misleading in normal-pressure hydrocephalus nork Neill R. Graff‐Radford
Argitaratua 2014Artigo -
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Alzheimer Disease nork Richard J. Caselli, Thomas G. Beach, David S. Knopman, Neill R. Graff‐Radford
Argitaratua 2017Revisão -
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Hippocampal Sclerosis in the Elderly nork Winnie Pao, Dennis W. Dickson, Julia E. Crook, NiCole A. Finch, Rosa Rademakers, Neill R. Graff‐Radford
Argitaratua 2011Artigo -
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Pathology and temporal onset of visual hallucinations, misperceptions and family misidentification distinguishes dementia with Lewy bodies from Alzheimer's disease nork Tanis J. Ferman, Zoe Arvanitakis, Hiroshige Fujishiro, Ranjan Duara, Francine Parfitt, M. Purdy, Carol Waters, Warren Barker, Neill R. Graff‐Radford, Dennis W. Dickson
Argitaratua 2012Artigo -
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Genetic variants in a haplotype block spanningIDE are significantly associated with plasma A?42 levels and risk for Alzheimer disease nork Nil�fer Ertekin-Taner, Mariet Allen, Daniel J. Fadale, Leah Scanlin, Linda H. Younkin, Ronald C. Petersen, Neill R. Graff‐Radford, Steven G. Younkin
Argitaratua 2004Artigo -
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Influence of comorbidities in idiopathic normal pressure hydrocephalus — research and clinical care. A report of the ISHCSF task force on comorbidities in INPH nork Jan Malm, Neill R. Graff‐Radford, Masatsune Ishikawa, Bjarne Winther Kristensen, Ville Leinonen, Etsuro Mori, Brian Owler, Mats Tullberg, Michael A. Williams, Norman Relkin
Argitaratua 2013Artigo -
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<i>Fus</i> gene mutations in familial and sporadic amyotrophic lateral sclerosis nork 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
Argitaratua 2010Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
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