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Molecular Genetics & Genomic Medicine|January 18, 2020
Compound heterozygous mutations in FBN1 in a large family with Marfan syndromeAideen M McInerney-Leo, Jennifer West, Lawrie Wheeler, et al.
Diabetes Technology & Therapeutics|August 18, 2025
Accuracy of Dexcom G6 Pro and G7 Continuous Glucose Monitors in Patients Treated with Maintenance DialysisLeila R Zelnick, Subbulaxmi Trikudanathan, Yoshio N Hall, et al.
JAMA Network Open|August 29, 2024
Persistent Neighborhood Poverty and Breast Cancer OutcomesJ C Chen, Demond Handley, Mohamed I Elsaid, et al.
Journal of Patient Safety|May 24, 2013
Patient safety event reporting expectation: does it influence residents' attitudes and reporting behaviors?Justin R Boike, Jared S Bortman, Jonathan M Radosta, et al.
Kidney International Reports|September 18, 2024
Corrigendum to "WCN24-813 MANAGEMENT OF ACUTE FLUID OVERLOAD IN HEART FAILURE PATIENTS WITH CKD USING HOME DELIVERED SUBCUTANEOUS FUROSEMIDE" [Kidney International Reports Volume 9, Issue 4, Supplement, April 2024, Page S251-S252]Rosa Montero, Ashwin Anenden, Jane Nokes, et al.
Frontiers in Cellular Neuroscience|November 30, 2020
DAPK1 Promotes Extrasynaptic GluN2B Phosphorylation and Striatal Spine Instability in the YAC128 Mouse Model of Huntington DiseaseMandi E Schmidt, Nicholas S Caron, Amirah E Aly, et al.
Biopreservation and Biobanking|August 7, 2026
The Nonhuman Primate Developmental Genotype-Tissue Expression Biospecimen and Histopathology ResourceJenna N Castro, Samia Silva de Castro, Rebecca L Linn, et al.
NPJ Breast Cancer|June 12, 2024
Allostatic load as a predictor of postoperative complications in patients with breast cancerJ C Chen, Mohamed I Elsaid, Demond Handley, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|April 29, 2016
Validation of T2* in-line analysis for tissue iron quantification at 1.5 TMohammed H Alam, Taigang He, Dominique Auger, et al.
Human Molecular Genetics|November 10, 2017
HACE1 is essential for astrocyte mitochondrial function and influences Huntington disease phenotypes in vivoDagmar E Ehrnhoefer, Amber L Southwell, Meenalochani Sivasubramanian, et al.
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