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The British Journal of Dermatology|October 2, 2020
Randomized controlled trial of topical corticosteroid and home-based narrowband ultraviolet B for active and limited vitiligo: results of the HI-Light Vitiligo TrialK S Thomas, J M Batchelor, P Akram, et al.JAMA Neurology|July 6, 2026
Antisense Oligonucleotide Tofersen Distribution in the Central Nervous System of SOD1-ALS Autopsy Tissue DonorsAmanda J Guise, Monica Thanawala Sellon, Shanu F Roemer, et al.Journal of the American Society of Nephrology : JASN|January 19, 2019
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Daniela A Braun, Kassaundra Amann, et al.Kidney International|September 13, 2017
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosisAnkana Daga, Amar J Majmundar, Daniela A Braun, et al.Science (New York, N.Y.)|July 5, 2008
Phanerozoic trends in the global diversity of marine invertebratesJohn Alroy, Martin Aberhan, David J Bottjer, et al.Proceedings of the National Academy of Sciences of the United States of America|June 24, 2026
Creating common virtual ground: Protocols to democratize open VR researchAnand P A van Zelderen, Theodore C Masters-Waage, Salvatore J Affinito, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUTSteve Seltzsam, Chunyan Wang, Bixia Zheng, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT familiesLea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.Clinical Journal of the American Society of Nephrology : CJASN|November 12, 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic SyndromeJillian K Warejko, Weizhen Tan, Ankana Daga, et al.Journal of the American Society of Nephrology : JASN|August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.Pageof 207