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International Braz J Urol : Official Journal of the Brazilian Society of Urology
|
January 28, 2017
Research prioritization of men's health and urologic diseases
Tyler Okland, Chante Karimkhani, Hannah Pederson, et al.
Transplantation
|
June 26, 2007
Two years postconversion from a prograf-based regimen to a once-daily tacrolimus extended-release formulation in stable kidney transplant recipients
Rita Alloway, Steven Steinberg, Kassem Khalil, 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 population
Sebastien Levesque, Charles Morin, Simon-Pierre Guay, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
November 6, 2010
Switching from calcineurin inhibitor-based regimens to a belatacept-based regimen in renal transplant recipients: a randomized phase II study
Lionel Rostaing, Pablo Massari, Valter Duro Garcia, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
July 24, 2012
Improvement in renal function in kidney transplant recipients switched from cyclosporine or tacrolimus to belatacept: 2-year results from the long-term extension of a phase II study
Josep Grinyo, Josefina Alberu, Fabiana L C Contieri, et al.
The New England Journal of Medicine
|
January 28, 2016
Belatacept and Long-Term Outcomes in Kidney Transplantation
Flavio Vincenti, Lionel Rostaing, Joseph Grinyo, et al.
Surgical Endoscopy
|
February 8, 2011
A comparison of outcomes between open and laparoscopic surgical repair of recurrent inguinal hernias
Nilay R Shah, Dean J Mikami, Charles Cook, et al.
Plos One
|
May 20, 2016
Common miR-590 Variant rs6971711 Present Only in African Americans Reduces miR-590 Biogenesis
Xiaoping Lin, Steven Steinberg, Suresh K Kandasamy, et al.
Plos Genetics
|
February 12, 2014
Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24
Caryline Agler, Dahlia M Nielsen, Ganokon Urkasemsin, et al.
Molecular Genetics and Metabolism
|
June 25, 2011
X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism
Ying Wang, Rachel Busin, Catherine Reeves, et al.
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Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
International Braz J Urol : Official Journal of the Brazilian Society of Urology
|
January 28, 2017
Research prioritization of men's health and urologic diseases
Tyler Okland, Chante Karimkhani, Hannah Pederson, et al.
Transplantation
|
June 26, 2007
Two years postconversion from a prograf-based regimen to a once-daily tacrolimus extended-release formulation in stable kidney transplant recipients
Rita Alloway, Steven Steinberg, Kassem Khalil, 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 population
Sebastien Levesque, Charles Morin, Simon-Pierre Guay, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
November 6, 2010
Switching from calcineurin inhibitor-based regimens to a belatacept-based regimen in renal transplant recipients: a randomized phase II study
Lionel Rostaing, Pablo Massari, Valter Duro Garcia, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
July 24, 2012
Improvement in renal function in kidney transplant recipients switched from cyclosporine or tacrolimus to belatacept: 2-year results from the long-term extension of a phase II study
Josep Grinyo, Josefina Alberu, Fabiana L C Contieri, et al.
The New England Journal of Medicine
|
January 28, 2016
Belatacept and Long-Term Outcomes in Kidney Transplantation
Flavio Vincenti, Lionel Rostaing, Joseph Grinyo, et al.
Surgical Endoscopy
|
February 8, 2011
A comparison of outcomes between open and laparoscopic surgical repair of recurrent inguinal hernias
Nilay R Shah, Dean J Mikami, Charles Cook, et al.
Plos One
|
May 20, 2016
Common miR-590 Variant rs6971711 Present Only in African Americans Reduces miR-590 Biogenesis
Xiaoping Lin, Steven Steinberg, Suresh K Kandasamy, et al.
Plos Genetics
|
February 12, 2014
Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24
Caryline Agler, Dahlia M Nielsen, Ganokon Urkasemsin, et al.
Molecular Genetics and Metabolism
|
June 25, 2011
X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism
Ying Wang, Rachel Busin, Catherine Reeves, et al.
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of 5