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Physical Review Letters|September 28, 2010
Density-dependent reorientation and rehybridization of chemisorbed conjugated molecules for controlling interface electronic structureB Bröker, O T Hofmann, G M Rangger, et al.Journal of the American Heart Association|November 10, 2023
Joint Associations of Pregnancy Complications and Postpartum Maternal Renal Biomarkers With Severe Cardiovascular Morbidities: A US Racially and Ethnically Diverse Prospective Birth Cohort StudyXiumei Hong, Avi Z Rosenberg, Jurgen Heymann, et al.Plos Genetics|March 5, 2016
Role of APOBEC3F Gene Variation in HIV-1 Disease Progression and Pneumocystis PneumoniaPing An, Sudhir Penugonda, Christian W Thorball, et al.American Journal of Nephrology|January 21, 2009
Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN studyBarry I Freedman, Jeffrey B Kopp, Cheryl A Winkler, et al.Stroke (Hoboken, N.J.)|January 23, 2026
Pressurized Contrast-Related Posterior Reversible Encephalopathy Syndrome After Cerebral Digital Subtraction AngiographyLea Scherschinski, Tyler D Schriber, Stefan W Koester, et al.World Neurosurgery|September 8, 2023
Occipital Artery to Middle Cerebral Artery Direct Bypass: A Salvage Revascularization Technique for Ischemic Moyamoya DiseaseJacob F Baranoski, Joshua S Catapano, Joseph H Garcia, et al.Frontiers in Genetics|February 3, 2023
Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2Yu Toyoda, Sung Kweon Cho, Velibor Tasic, et al.World Neurosurgery|July 8, 2023
Factors Associated with Unfavorable Clinical Presentations in Patients with Ruptured BrainArteriovenous MalformationsJoseph H Garcia, Luis Carrete, W Caleb Rutledge, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 19, 2020
Clinical outcomes after revascularization for pediatric moyamoya disease and syndrome: A single-center seriesRamin A Morshed, Adib A Abla, Daniel Murph, et al.Kidney International|May 21, 2015
Sequencing rare and common APOL1 coding variants to determine kidney disease riskSophie Limou, George W Nelson, Laurence Lecordier, et al.Pageof 95