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Hepatology (Baltimore, Md.)|November 26, 2008
Naturally occurring dominant resistance mutations to hepatitis C virus protease and polymerase inhibitors in treatment-naïve patientsThomas Kuntzen, Joerg Timm, Andrew Berical, et al.
Kidney International|July 3, 2009
The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification, Daniel C Cattran, Rosanna Coppo, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 18, 2019
Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basisKarin Weiss, Hayley P Lazar, Alina Kurolap, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 8, 2019
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basisKarin Weiss, Hayley P Lazar, Alina Kurolap, et al.
Kidney International|March 5, 2010
The Oxford IgA nephropathy clinicopathological classification is valid for children as well as adults, Rosanna Coppo, Stéphan Troyanov, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 13, 2018
Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) updateRosanna Coppo, Graziella D'Arrigo, Giovanni Tripepi, et al.
JAMA|June 20, 2024
A Clinical Diagnostic Test for Calcium Release Deficiency SyndromeMingke Ni, Ziv Dadon, Julian O M Ormerod, et al.
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