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Molecular Genetics and Metabolism|November 16, 2004
The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrumSteven Steinberg, Li Chen, Liumei Wei, et al.
Journal of Endourology|June 13, 2019
Is Your Career Hurting You? The Ergonomic Consequences of Surgery in 701 Urologists WorldwideGranville L Lloyd, Amanda S J Chung, Steven Steinberg, et al.
Clinical Transplants|August 7, 2014
Immunoglobulin G subclass analysis of HLA donor specific antibodies in heart and renal transplant recipientsJames C Cicciarelli, Noriyuki Kasahara, Nathan A Lemp, et al.
Molecular Genetics and Metabolism|January 12, 2010
A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeletonNancy Braverman, Rui Zhang, Li Chen, et al.
The American Surgeon|December 15, 2010
The use of extracorporeal membrane oxygenation in severe necrotizing soft tissue infections complicated by septic shockMichael S Firstenberg, Erik Abel, Danielle Blais, et al.
Transplantation Direct|April 14, 2017
mTOR Inhibition by Everolimus Does Not Impair Closure of Punch Biopsy Wounds in Renal Transplant PatientsShelley B Dutt, Josephine Gonzales, Megan Boyett, et al.
Kidney International Reports|July 26, 2021
A Randomized Trial of Roxadustat in Anemia of Kidney Failure: SIERRAS StudyChaim Charytan, Roberto Manllo-Karim, Edouard R Martin, et al.
International Braz J Urol : Official Journal of the Brazilian Society of Urology|January 28, 2017
Research prioritization of men's health and urologic diseasesTyler Okland, Chante Karimkhani, Hannah Pederson, et al.
BMC Medical Genetics|August 17, 2012
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian populationSebastien Levesque, Charles Morin, Simon-Pierre Guay, et al.
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