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European Journal of Endocrinology|June 22, 2023
Natural history of non-functioning pituitary microadenomas: results from the UK non-functioning pituitary adenoma consortiumRoss Hamblin, Athanasios Fountas, Kirstie Lithgow, et al.
JCI Insight|October 18, 2022
Culture media composition influences patient-derived organoid ability to predict therapeutic responses in gastrointestinal cancersTara L Hogenson, Hao Xie, William J Phillips, et al.
Diabetes Care|July 23, 2024
A Randomized Comparison of Postprandial Glucose Excursion Using Inhaled Insulin Versus Rapid-Acting Analog Insulin in Adults With Type 1 Diabetes Using Multiple Daily Injections of Insulin or Automated Insulin DeliveryIrl B Hirsch, Roy W Beck, Martin Chase Marak, et al.
The New England Journal of Medicine|September 8, 2010
Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedemaMarco Cicardi, Aleena Banerji, Francisco Bracho, et al.
The New England Journal of Medicine|March 19, 2025
A Randomized Trial of Automated Insulin Delivery in Type 2 DiabetesYogish C Kudva, Dan Raghinaru, John W Lum, et al.
Obstetrical & Gynecological Survey|December 30, 2025
A Randomized Trial of Automated Insulin Delivery in Type 2 DiabetesYogish C Kudva, Dan Raghinaru, John W Lum, et al.
American Journal of Human Genetics|February 20, 2025
Pathogenic de novo variants in PPP2R5C cause a neurodevelopmental disorder within the Houge-Janssens syndrome spectrumIris Verbinnen, Sofia Douzgou Houge, Tzung-Chien Hsieh, et al.
Gastrointestinal Endoscopy|February 14, 2016
EUS Needle Identification Comparison and Evaluation study (with videos)Shou-Jiang Tang, Andreas S Vilmann, Adrian Saftoiu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 31, 2024
Expanding the phenotype and genotype spectrum of TAOK1 neurodevelopmental disorder and delineating TAOK2 neurodevelopmental disorderNour Elkhateeb, Renarta Crookes, Michael Spiller, et al.
Nature Genetics|April 8, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changesRocio Rius, Alexander J M Blakes, Yuyang Chen, et al.
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