Zika Virus infection and Guillain-Barré syndrome in Northeastern Mexico: A case-control study.

Autor: Fernando Gongora-Rivera, Israel Grijalva, Adrian Infante-Valenzuela, Carlos Cámara-Lemarroy, Elvira Garza-González, Martin Paredes-Cruz, Concepción Grajales-Muñiz, José Guerrero-Cantera, Ignacio Vargas-Ramos, Jesus Soares, Joseph Y Abrams, Ashley R Styczynski, Adrián Camacho-Ortiz, Margarita E Villarino, Ermias D Belay, Lawrence B Schonberger, James J Sejvar, GBS HU-IMSS Working Group

Publikováno v: PLoS ONE, Vol 15, Iss 3, p e0230132 (2020)

BackgroundBeginning August 2017, we conducted a prospective case-control investigation in Monterrey, Mexico to assess the association between Zika virus (ZIKV) and Guillain-Barré syndrome (GBS).MethodsFor each of 50 GBS case-patients, we enrolled 2-

Externí odkaz: https://doaj.org/article/b57b87dd378642c098f0504c55c7a196

Increased rates of Guillain-Barré syndrome associated with Zika virus outbreak in the Salvador metropolitan area, Brazil.

Autor: Ashley R Styczynski, Juliane M A S Malta, Elisabeth R Krow-Lucal, Jadher Percio, Martha E Nóbrega, Alexander Vargas, Tatiana M Lanzieri, Priscila L Leite, J Erin Staples, Marc X Fischer, Ann M Powers, Gwong-Jen J Chang, P L Burns, Erin M Borland, Jeremy P Ledermann, Eric C Mossel, Lawrence B Schonberger, Ermias B Belay, Jorge L Salinas, Roberto D Badaro, James J Sejvar, Giovanini E Coelho

Publikováno v: PLoS Neglected Tropical Diseases, Vol 11, Iss 8, p e0005869 (2017)

In mid-2015, Salvador, Brazil, reported an outbreak of Guillain-Barré syndrome (GBS), coinciding with the introduction and spread of Zika virus (ZIKV). We found that GBS incidence during April-July 2015 among those ≥12 years of age was 5.6 cases/1

Externí odkaz: https://doaj.org/article/8f7c5fe229014028ab3cc7ba0aa921f7

Human prion diseases in the United States.

Autor: Robert C Holman, Ermias D Belay, Krista Y Christensen, Ryan A Maddox, Arialdi M Minino, Arianne M Folkema, Dana L Haberling, Teresa A Hammett, Kenneth D Kochanek, James J Sejvar, Lawrence B Schonberger

Publikováno v: PLoS ONE, Vol 5, Iss 1, p e8521 (2010)

BackgroundPrion diseases are a family of rare, progressive, neurodegenerative disorders that affect humans and animals. The most common form of human prion disease, Creutzfeldt-Jakob disease (CJD), occurs worldwide. Variant CJD (vCJD), a recently eme

Externí odkaz: https://doaj.org/article/480beb80972e4d89bb002f1131dbca25

Corticosteroids Added to Initial Intravenous Immunoglobulin Treatment for the Prevention of Coronary Artery Abnormalities in High‐Risk Patients With Kawasaki Disease

Autor: Ryusuke Ae, Joseph Y. Abrams, Ryan A. Maddox, Lawrence B. Schonberger, Yosikazu Nakamura, Masanari Kuwabara, Nobuko Makino, Yuri Matsubara, Koki Kosami, Teppei Sasahara, Ermias D. Belay

Publikováno v: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 9, Iss 17 (2020)

BACKGROUND Randomized controlled trials previously provided different conclusions about the superiority of adding corticosteroids to initial intravenous immunoglobulin treatment for the prevention of coronary artery abnormalities in patients with Kaw

Externí odkaz: https://doaj.org/article/ca24626b7d5d4910a0653decf8e2437f

A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI

Autor: Vikram Venkatraghavan, Riccardo Pascuzzo, Esther E. Bron, Marco Moscatelli, Marina Grisoli, Amy Pickens, Mark L. Cohen, Lawrence B. Schonberger, Pierluigi Gambetti, Brian S. Appleby, Stefan Klein, Alberto Bizzi

Publikováno v: Alzheimer's and Dementia. Elsevier Inc.
Venkatraghavan, V, Pascuzzo, R, Bron, E E, Moscatelli, M, Grisoli, M, Pickens, A, Cohen, M L, Schonberger, L B, Gambetti, P, Appleby, B S, Klein, S & Bizzi, A 2023, ' A discriminative event-based model for subtype diagnosis of sporadic Creutzfeldt-Jakob disease using brain MRI ', Alzheimer's and Dementia . https://doi.org/10.1002/alz.12939
Alzheimer's and Dementia. Elsevier

Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, MV2C, MV2K, VV1, and VV2) with distinct disease durations and spatiotemporal cascades of brain lesions. Our goal was to establish the ante mortem diag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1fcd0a44219e175387db8a10837134
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