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Bone|February 8, 2017
Unexpected widespread hypophosphatemia and bone disease associated with elemental formula use in infants and childrenLuisa F Gonzalez Ballesteros, Nina S Ma, Rebecca J Gordon, et al.
Trends in Psychiatry and Psychotherapy|August 27, 2020
Cross-cultural adaptation of the Internet Gaming Disorder Scale - Short Form (IGDS9-SF) to the Brazilian contextMariana F Donadon, Marcos H N Chagas, Thiago D Apolinário-da-Silva, et al.
Global Food Security|September 13, 2021
Emerging COVID-19 impacts, responses, and lessons for building resilience in the seafood systemDavid C Love, Edward H Allison, Frank Asche, et al.
Cancer Causes & Control : CCC|July 19, 2013
The California Breast Cancer Survivorship Consortium (CBCSC): prognostic factors associated with racial/ethnic differences in breast cancer survivalAnna H Wu, Scarlett Lin Gomez, Cheryl Vigen, et al.
Science (New York, N.Y.)|November 20, 2025
The synaptic ectokinase VLK triggers the EphB2-NMDAR interaction to drive injury-induced painKolluru D Srikanth, Hajira Elahi, Praveen Chander, et al.
Journal of the National Cancer Institute|November 17, 2005
Lifetime recreational exercise activity and breast cancer risk among black women and white womenLeslie Bernstein, Alpa V Patel, Giske Ursin, et al.
Bioorganic & Medicinal Chemistry Letters|September 18, 2012
Preparation and optimization of new 4-(morpholin-4-yl)-(6-oxo-1,6-dihydropyrimidin-2-yl)amide derivatives as PI3Kβ inhibitorsVictor Certal, Frank Halley, Angela Virone-Oddos, et al.
The Lancet. Infectious Diseases|October 10, 2024
Aztreonam-avibactam versus meropenem for the treatment of serious infections caused by Gram-negative bacteria (REVISIT): a descriptive, multinational, open-label, phase 3, randomised trialYehuda Carmeli, José Miguel Cisneros, Mical Paul, et al.
Annals of the Rheumatic Diseases|May 1, 2026
Impact of tofacitinib on growth in patients with juvenile idiopathic arthritisHermine I Brunner, Mittermayer Santiago, Beth Gottlieb, et al.
Human Mutation|February 11, 2011
Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis ComplexMarianne Hoogeveen-Westerveld, Marjolein Wentink, Diana van den Heuvel, et al.
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