Yvonne Cohen
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Explore the profile of Yvonne Cohen including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
Bayazid R, Orru C, Aslam R, Cohen Y, Silva-Rohwer A, Lee S, et al.
Acta Neuropathol
. 2023 May;
146(1):167-170.
PMID: 37253983
No abstract available.
2.
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques
Bayazid R, Orru C, Aslam R, Cohen Y, Silva-Rohwer A, Lee S, et al.
Acta Neuropathol
. 2023 May;
146(1):121-143.
PMID: 37156880
The presence of amyloid kuru plaques is a pathological hallmark of sporadic Creutzfeldt-Jakob disease (sCJD) of the MV2K subtype. Recently, PrP plaques (p) have been described in the white matter...
3.
Ryan C, Mac Hale D, Cohen Y
Arch Dis Child
. 2017 Feb;
102(8):693-694.
PMID: 28235836
No abstract available.
4.
Foutz A, Appleby B, Hamlin C, Liu X, Yang S, Cohen Y, et al.
Ann Neurol
. 2016 Nov;
81(1):79-92.
PMID: 27893164
Objective: Several prion amplification systems have been proposed for detection of prions in cerebrospinal fluid (CSF), most recently, the measurements of prion seeding activity with second-generation real-time quaking-induced conversion (RT-QuIC)....
5.
Umeh C, Kalakoti P, Greenberg M, Notari S, Cohen Y, Gambetti P, et al.
Mov Disord Clin Pract
. 2016 Sep;
3(4):355-358.
PMID: 27617269
Parkinsonism-dystonia is rare in carriers of PRNP P102L mutation. Severity and distribution of prion protein (PrP) deposition may influence the clinical presentation. We present such clinic-pathological correlation in a 56-year-old...
6.
Minikel E, Vallabh S, Lek M, Estrada K, Samocha K, Sathirapongsasuti J, et al.
Sci Transl Med
. 2016 Jan;
8(322):322ra9.
PMID: 26791950
More than 100,000 genetic variants are reported to cause Mendelian disease in humans, but the penetrance-the probability that a carrier of the purported disease-causing genotype will indeed develop the disease-is...
7.
Maheshwari A, Fischer M, Gambetti P, Parker A, Ram A, Soto C, et al.
Emerg Infect Dis
. 2015 Apr;
21(5):750-9.
PMID: 25897712
Variant Creutzfeldt-Jakob disease (vCJD) is a rare, fatal prion disease resulting from transmission to humans of the infectious agent of bovine spongiform encephalopathy. We describe the clinical presentation of a...
8.
Safar J, Xiao X, Kabir M, Chen S, Kim C, Haldiman T, et al.
PLoS Pathog
. 2015 Apr;
11(4):e1004832.
PMID: 25875953
The infectious pathogen responsible for prion diseases is the misfolded, aggregated form of the prion protein, PrPSc. In contrast to recent progress in studies of laboratory rodent-adapted prions, current understanding...
9.
Cohen M, Kim C, Haldiman T, ElHag M, Mehndiratta P, Pichet T, et al.
Brain
. 2015 Feb;
138(Pt 4):1009-22.
PMID: 25688081
Genetic and environmental factors that increase the risk of late-onset Alzheimer disease are now well recognized but the cause of variable progression rates and phenotypes of sporadic Alzheimer's disease is...
10.
Notari S, Xiao X, Espinosa J, Cohen Y, Qing L, Aguilar-Calvo P, et al.
Emerg Infect Dis
. 2014 Nov;
20(12):2006-14.
PMID: 25418590
Variably protease-sensitive prionopathy (VPSPr), a recently identified and seemingly sporadic human prion disease, is distinct from Creutzfeldt-Jakob disease (CJD) but shares features of Gerstmann-Sträussler-Scheinker disease (GSS). However, contrary to exclusively...