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European Journal of Heart Failure|December 7, 2019
Selenium and outcome in heart failureNils Bomer, Niels Grote Beverborg, Martijn F Hoes, et al.
The Journal of Clinical Endocrinology and Metabolism|October 15, 2010
Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous familyEva Morava, Jirko Kühnisch, Jefte M Drijvers, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 28, 2020
Reduced Vitamin K Status as a Potentially Modifiable Risk Factor of Severe Coronavirus Disease 2019Anton S M Dofferhoff, Ianthe Piscaer, Leon J Schurgers, et al.
Journal of the American College of Cardiology|August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathyAnnalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Cardiovascular Diabetology|September 19, 2020
Circulating Receptor Activator of Nuclear Factor kB Ligand and triglycerides are associated with progression of lower limb arterial calcification in type 2 diabetes: a prospective, observational cohort studyOlivier Bourron, Franck Phan, Mamadou Hassimiou Diallo, et al.
Ecology|October 7, 2025
Habitat fidelity in hawksbill sea turtlesAndrew S Maurer, Julia A Horrocks, Claudio Bellini, et al.
Virchows Archiv : an International Journal of Pathology|January 14, 2022
Cell-of-origin classification using the Hans and Lymph2Cx algorithms in primary cutaneous large B-cell lymphomasAnne M R Schrader, Ruben A L de Groen, Rein Willemze, et al.
The Journal of Pediatrics|May 24, 2020
A Phase II Randomized Clinical Trial of the Safety and Efficacy of Intravenous Umbilical Cord Blood Infusion for Treatment of Children with Autism Spectrum DisorderGeraldine Dawson, Jessica M Sun, Jennifer Baker, et al.
Nature Immunology|February 15, 2024
IL-23 stabilizes an effector T<sub>reg</sub> cell program in the tumor microenvironmentTobias Wertheimer, Pascale Zwicky, Lukas Rindlisbacher, et al.
Human Mutation|May 8, 2026
Variant Curation of the Largest Compendium of <i>FOXL2</i> Coding and Noncoding Sequence and Structural Variants in BPESCharlotte Matton, Julie Van De Velde, Marieke De Bruyne, et al.
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