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American Journal of Medical Genetics. Part A|October 12, 2020
Immune dysfunction in MGAT2-CDG: A clinical report and review of the literatureSheri A Poskanzer, Matthew J Schultz, Coleman T Turgeon, et al.Cancer Cell|September 29, 2023
Loss of p53 and mutational heterogeneity drives immune resistance in an autochthonous mouse lung cancer model with high tumor mutational burdenMingrui Zhu, Jiwoong Kim, Qing Deng, et al.The Canadian Journal of Cardiology|December 14, 2020
Anticoagulation for Patients With Atrial Fibrillation and End-Stage Renal Disease on Dialysis: A National SurveyLaura F Halperin, May K Lee, Janet Liew, et al.JCI Insight|July 27, 2018
Extreme erythrocyte macrocytic and microcytic percentages are highly predictive of morbidity and mortalityBenjamin D Horne, Joseph B Muhlestein, Sterling T Bennett, et al.Nature Genetics|November 14, 1997
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB GroupS T Bennett, A J Wilson, L Esposito, et al.Heart Rhythm|August 27, 2013
The Canadian experience with Durata and Riata ST Optim defibrillator leads: a report from the Canadian Heart Rhythm Society Device CommitteeMatthew T Bennett, Andrew C T Ha, Derek V Exner, et al.American Journal of Human Genetics|August 5, 2005
Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26Susan A Treloar, Jacqueline Wicks, Dale R Nyholt, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowthTara L Wenger, Sheila Ganti, Catherine Bull, et al.Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|June 23, 2022
Randomized trial of conventional versus radiofrequency needle transseptal puncture for cryoballoon ablation: the CRYO-LATS trialJason G Andrade, Laurent Macle, Matthew T Bennett, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2026
Mutations in VCP cause Adams-Oliver syndrome with or without pulmonary hypertensionAnna Lehman, Sana Ahmed, Arezoo Mohajeri, et al.Pageof 76