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Kidney International|August 1, 2000
Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's diseaseT Igarashi, J Inatomi, T Ohara, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2005
A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): mutational analysis, phenotypic variability and treatment challengesC P Burren, A Curley, P Christie, et al.
Free Radical Biology & Medicine|May 27, 2005
JNK activation limits dendritic cell maturation in response to reactive oxygen species by the induction of apoptosisMatthew E Handley, Manish Thakker, Gabriele Pollara, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|May 25, 2022
Can a Situational Judgment Test Identify Trainees at Risk of Professionalism Issues? A Multi-Institutional, Prospective Cohort StudyMichael J Cullen, Charlene Zhang, Paul R Sackett, et al.
Nature Reviews. Endocrinology|November 17, 2018
The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseasesFadil M Hannan, Enikö Kallay, Wenhan Chang, et al.
Journal of Assisted Reproduction and Genetics|March 22, 2022
Sociodemographic differences in utilization of fertility services among reproductive age women diagnosed with cancer in the USAPaxton Voigt, Jesse Persily, Jennifer K Blakemore, et al.
Studies in Health Technology and Informatics|September 16, 2010
Why don't innovation models help with informatics implementations?Rod Ward
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