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Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|October 27, 2025
Incremental start and clinical outcomes in peritoneal dialysis: International results from PDOPPSAshik Hayat, Melissa S Cheetham, Yeoungjee Cho, et al.Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|September 18, 2025
Validating the standardised outcomes in nephrology-life participation (SONG-LP) measure in people receiving peritoneal dialysis: Rationale and processCameron Thomas Burnett, Allison Jaure, Anastasia Hughes, et al.Ebiomedicine|September 15, 2024
Tissue-specific TCF4 triplet repeat instability revealed by optical genome mappingChristina Zarouchlioti, Stephanie Efthymiou, Stefano Facchini, et al.Paediatric and Perinatal Epidemiology|October 16, 2012
Trends in the use of antiepileptic drugs among pregnant women in the US, 2001-2007: a medication exposure in pregnancy risk evaluation program studyWilliam V Bobo, Robert L Davis, Sengwee Toh, et al.Ophthalmology Science|January 15, 2025
Visual Acuity, Full-field Stimulus Thresholds, and Electroretinography for 4 Years in The Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) StudyDavid G Birch, Peiyao Cheng, Maureen G Maguire, et al.Plos One|March 14, 2012
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapyMei Hong Tan, Donna S Mackay, Jill Cowing, et al.Plos Genetics|May 7, 2024
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated diseaseNihar Bhattacharyya, Niuzheng Chai, Nathaniel J Hafford-Tear, et al.Genome Research|June 21, 2022
Somatic retrotransposition in the developing rhesus macaque brainVictor Billon, Francisco J Sanchez-Luque, Jay Rasmussen, et al.American Journal of Human Genetics|February 1, 2025
Inter-chromosomal insertions at Xq27.1 associated with retinal dystrophy induce dysregulation of LINC00632 and CDR1as/ciRS-7Jessica C Gardner, Katarina Jovanovic, Daniele Ottaviani, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
DLG2 variants in patients with pubertal disordersYoun Hee Jee, Sehoon Won, Julian C Lui, et al.Pageof 149