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Dementia and Geriatric Cognitive Disorders|March 23, 2021
Neurobehavioral Characteristics of FDG-PET Defined Right-Dominant Semantic Dementia: A Longitudinal StudyAlexis X Curet Burleson, Nha Trang Thu Pham, Marina Buciuc, et al.
Antiviral Research|March 12, 2022
A highly sensitive cell-based luciferase assay for high-throughput automated screening of SARS-CoV-2 nsp5/3CLpro inhibitorsK Y Chen, T Krischuns, L Ortega Varga, et al.
The Journal of Allergy and Clinical Immunology|May 11, 2021
Neutralizing anti-IL-1 receptor antagonist autoantibodies induce inflammatory and fibrotic mediators in IgG4-related diseaseJustin A Jarrell, Matthew C Baker, Cory A Perugino, et al.
European Journal of Neurology|February 17, 2015
Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance imagesJ L Whitwell, B F Boeve, S D Weigand, et al.
Annals of the Rheumatic Diseases|July 21, 2026
A phase 2 trial of rilzabrutinib in IgG4-related diseaseJohn H Stone, Mollie Carruthers, Matthew C Baker, et al.
Journal of the American College of Radiology : JACR|May 26, 2023
ACR Appropriateness Criteria® Soft Tissue Masses: 2022 Update, Hillary W Garner, Daniel E Wessell, et al.
American Journal of Human Genetics|April 9, 2013
A mechanism for controlled access to GWAS data: experience of the GAIN Data Access CommitteeErin M Ramos, Corina Din-Lovinescu, Ebony B Bookman, et al.
The Journal of Trauma|July 11, 2009
Hemostatic resuscitation during surgery improves survival in patients with traumatic-induced coagulopathyJuan C Duchesne, Tareq M Islam, Lance Stuke, et al.
Research on Child and Adolescent Psychopathology|January 21, 2022
Parental Knowledge/Monitoring and Depressive Symptoms During Adolescence: Protective Factor or Spurious Association?William E Pelham, Susan F Tapert, Marybel R Gonzalez, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.
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