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Clinical Journal of the American Society of Nephrology : CJASN|September 10, 2011
Cardiac magnetic resonance assessment of left ventricular mass in autosomal dominant polycystic kidney diseaseRonald D Perrone, Kaleab Z Abebe, Robert W Schrier, et al.Kidney International|December 30, 2011
Analysis of baseline parameters in the HALT polycystic kidney disease trialsVicente E Torres, Arlene B Chapman, Ronald D Perrone, et al.Revista De Gastroenterologia De Mexico (English)|April 25, 2019
The Mexican consensus on the diagnosis and treatment of diverticular disease of the colonR Raña-Garibay, N Salgado-Nesme, R Carmona-Sánchez, et al.Cancer Discovery|March 24, 2018
The Pancreatic Cancer Microbiome Promotes Oncogenesis by Induction of Innate and Adaptive Immune SuppressionSmruti Pushalkar, Mautin Hundeyin, Donnele Daley, et al.Gastroenterology|December 15, 2023
Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver DiseaseRia Schönauer, Dana Sierks, Melissa Boerrigter, et al.BMC Cancer|February 15, 2018
HIPECT4: multicentre, randomized clinical trial to evaluate safety and efficacy of Hyperthermic intra-peritoneal chemotherapy (HIPEC) with Mitomycin C used during surgery for treatment of locally advanced colorectal carcinomaA Arjona-Sánchez, P Barrios, E Boldo-Roda, et al.ESMO Open|June 25, 2025
Hyalinization-based pathologic response and immune infiltration following neoadjuvant radiotherapy with or without immune-checkpoint blockade in localized undifferentiated pleomorphic sarcomaR S Traweek, M Zoghbi, R Lazcano, et al.Emerging Infectious Diseases|July 11, 2026
Virulence of Burkholderia pseudomallei Strains from Western Hemisphere and Africa in MiceChristopher P Klimko, J Matthew Meinig, Kevin D Mlynek, et al.American Journal of Human Genetics|December 10, 2021
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotypeSarah R Senum, Ying Sabrina M Li, Katherine A Benson, et al.Nature Genetics|January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk ratUrsula M Smith, Mark Consugar, Louise J Tee, et al.Pageof 125