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Author Details
Full Name
Brian S Appleby
Affiliation
Case Western Reserve University
ORCID
Career Start Year
2005
Papers
107
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36749840
A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI.
Alzheimers Dement
2023
37156880
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques.
Acta Neuropathol
2023
36949796
Creutzfeldt-Jakob Disease Misdiagnosed as Multiple System Atrophy.
Mov Disord Clin Pract
2023
37253983
Correction: A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques.
Acta Neuropathol
2023
37180971
Feasibility and acceptability of remote smartphone cognitive testing in frontotemporal dementia research.
Alzheimers Dement (Amst)
2023
36977552
Plasma inflammation for predicting phenotypic conversion and clinical progression of autosomal dominant frontotemporal lobar degeneration.
J Neurol Neurosurg Psychiatry
2023
37431188
Network Connectivity Alterations across the MAPT Mutation Clinical Spectrum.
Ann Neurol
2023
36591730
Multisite ALLFTD study modeling progressive empathy loss from the earliest stages of behavioral variant frontotemporal dementia.
Alzheimers Dement
2023
35262719
Prevalence of Surgical Procedures at Symptomatic Onset of Prion Disease.
JAMA Netw Open
2022
35614914
Atypical Case of VV1 Creutzfeldt-Jakob Disease Subtype: Case Report.
Front Neurol
2022
35584922
Sensitivity of the Social Behavior Observer Checklist to Early Symptoms of Patients With Frontotemporal Dementia.
Neurology
2022
35349636
Proposed research criteria for prodromal behavioural variant frontotemporal dementia.
Brain
2022
35790423
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar Degeneration.
Neurology
2022
36277922
Genetic aspects of human prion diseases.
Front Neurol
2022
34854532
The contribution of behavioral features to caregiver burden in FTLD spectrum disorders.
Alzheimers Dement
2022
35172059
Case 5-2022: A 65-Year-Old Woman with Rapidly Progressive Weakness in the Right Arm and Recurrent Falls.
N Engl J Med
2022
33274461
Subtype Diagnosis of Sporadic Creutzfeldt-Jakob Disease with Diffusion Magnetic Resonance Imaging.
Ann Neurol
2021
33827706
Streamlined alpha-synuclein RT-QuIC assay for various biospecimens in Parkinson's disease and dementia with Lewy bodies.
Acta Neuropathol Commun
2021
33766126
Two distinct conformers of PrP<sup>D</sup> type 1 of sporadic Creutzfeldt-Jakob disease with codon 129VV genotype faithfully propagate in vivo.
Acta Neuropathol Commun
2021
33925126
Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease.
Viruses
2021
33609480
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
Lancet Neurol
2021
33857770
Recognition memory and divergent cognitive profiles in prodromal genetic frontotemporal dementia.
Cortex
2021
34497065
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person.
Neurology
2021
34578375
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion.
Viruses
2021
34324063
Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Acta Neuropathol
2021
31272932
Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration.
Alzheimers Dement
2020
32001774
Co-existence of PrP<sup>D</sup> types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics.
Sci Rep
2020
31757870
Prion disease incidence in the United States: 2003-2015.
Neurology
2020
31784375
Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration.
Alzheimers Dement
2020
31953922
A case report of genetic prion disease with two different PRNP variants.
Mol Genet Genomic Med
2020
31914230
Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint.
Alzheimers Dement
2020
31914218
Utility of the global CDR[®] plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium.
Alzheimers Dement
2020
31914217
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.
Alzheimers Dement
2020
33064135
Human Prion Disease Surveillance in Washington State, 2006-2017.
JAMA Netw Open
2020
32571851
Diagnosis of prion diseases by RT-QuIC results in improved surveillance.
Neurology
2020
32733203
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a <i>De Novo</i> Seven-Octapeptide Repeat Insertion.
Front Cell Neurosci
2020
32949544
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
Lancet Neurol
2020
32478816
Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging.
JAMA Neurol
2020
32560672
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease.
Acta Neuropathol Commun
2020
32535770
Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt-Jakob disease.
Acta Neuropathol
2020
32371446
Revised Self-Monitoring Scale: A potential endpoint for frontotemporal dementia clinical trials.
Neurology
2020
30612334
In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP<sup>V180I</sup> Mutation.
Mol Neurobiol
2019
31872042
Nonlinear Z-score modeling for improved detection of cognitive abnormality.
Alzheimers Dement (Amst)
2019
31366689
Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease.
J Clin Microbiol
2019
31337719
Chronic Wasting Disease in Cervids: Implications for Prion Transmission to Humans and Other Animal Species.
mBio
2019
30861521
Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance.
Dement Geriatr Cogn Disord
2019
31008724
Human prion diseases.
Curr Opin Infect Dis
2019
30914754
PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission study.
Sci Rep
2019
30718499
Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals.
Nat Commun
2019
30651538
Early preclinical detection of prions in the skin of prion-infected animals.
Nat Commun
2019
1 - 50 of 107
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Rosa Rademakers
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Giovanni Coppola
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Tatiana Foroud
Indiana University School of Medicine
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Diana R Kerwin
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Peter V Rabins
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