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Journal of Immunology (Baltimore, Md. : 1950)|July 23, 2003
Promiscuous CTL recognition of viral epitopes on multiple human leukocyte antigens: biological validation of the proposed HLA A24 supertypeScott R Burrows, Rebecca A Elkington, John J Miles, et al.
BMC Pediatrics|August 3, 2018
Twin-to-twin transfusion syndrome neurodevelopmental follow-up study (neurodevelopmental outcomes for children whose twin-to-twin transfusion syndrome was treated with placental laser photocoagulation)Christie Bolch, Michael Fahey, Dinah Reddihough, et al.
Obstetrical & Gynecological Survey|January 20, 2026
Intrapartum Sildenafil to Improve Perinatal Outcomes: A Randomized Clinical TrialSailesh Kumar, William Tarnow-Mordi, Ben W Mol, et al.
American Journal of Medical Genetics. Part A|July 12, 2020
A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndromeMeredith Curtis, Danielle Baribeau, Susan Walker, et al.
JAMA|June 9, 2025
Intrapartum Sildenafil to Improve Perinatal Outcomes: A Randomized Clinical TrialSailesh Kumar, William Tarnow-Mordi, Ben W Mol, et al.
Clinical Drug Investigation|June 28, 2018
Effect of Renal Impairment on the Pharmacokinetics and Pharmacodynamics of Verinurad, a Selective Uric Acid Reabsorption InhibitorWilliam B Smith, Jesse Hall, Jolene K Berg, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 22, 2019
Relative contributions of diabetes and chronic kidney disease to neuropathy development in diabetic nephropathy patientsTushar Issar, Ria Arnold, Natalie C G Kwai, et al.
Cancer Drug Resistance (Alhambra, Calif.)|September 30, 2022
A nano-enhanced vaccine for metastatic melanoma immunotherapyKatelyn E Salotto, Walter C Olson, Karlyn E Pollack, et al.
NPJ Genomic Medicine|December 22, 2017
Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosageBreanne Dale, Bonnie MacKinnon Modi, Sanne Jilderda, et al.
NPJ Genomic Medicine|June 27, 2017
Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genesMarc Woodbury-Smith, Rob Nicolson, Mehdi Zarrei, et al.
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