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American Journal of Ophthalmology|May 14, 2017
Measurement and Reproducibility of Preserved Ellipsoid Zone Area and Preserved Retinal Pigment Epithelium Area in Eyes With ChoroideremiaAmir H Hariri, Swetha B Velaga, Aniz Girach, et al.
Human Molecular Genetics|August 1, 1997
Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groupsM P Marron, L J Raffel, H J Garchon, et al.
The Journal of Experimental Medicine|February 4, 2010
Chronic mucocutaneous candidiasis in APECED or thymoma patients correlates with autoimmunity to Th17-associated cytokinesKai Kisand, Anette S Bøe Wolff, Katarina Trebusak Podkrajsek, et al.
Physical Review Letters|September 10, 2025
Demonstration of a Novel Radiochemical Mix Diagnostic for Fusion Implosions at the National Ignition FacilityS A MacLaren, E L Dewald, D A Martinez, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophyKornelia Neveling, Lilian A Martinez-Carrera, Irmgard Hölker, et al.
Seminars in Dialysis|June 4, 2014
Guidelines for reporting case studies on extracorporeal treatments in poisonings: methodologyValéry Lavergne, Georges Ouellet, Josée Bouchard, et al.
Critical Care Medicine|January 20, 2026
Conversion From Venovenous to Venoarterial or Hybrid Extracorporeal Membrane Oxygenation: Analysis From the Extracorporeal Life Support Organization RegistryMaria Elena De Piero, Francesco Alessandri, Silvia Mariani, et al.
JCI Insight|February 8, 2024
Predictors of HIV rebound differ by timing of antiretroviral therapy initiationJonathan Z Li, Meghan Melberg, Autumn Kittilson, et al.
Nature Communications|January 9, 2021
HIV-1 diversity considerations in the application of the Intact Proviral DNA Assay (IPDA)Natalie N Kinloch, Yanqin Ren, Winiffer D Conce Alberto, et al.
Nature Medicine|February 26, 2020
Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGRJasmina Cehajic-Kapetanovic, Kanmin Xue, Cristina Martinez-Fernandez de la Camara, et al.
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