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Timothy H J Goodship

Showing results (41-50 of 78) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 25, 2006
Complement factor H-associated atypical hemolytic uremic syndrome in monozygotic twins: concordant presentation, discordant response to treatmentJean-Claude Davin, Karolien H Olie, René Verlaak, et al.
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Immunobiology|June 9, 2016
Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndromePatrick J Gleeson, Valerie Wilson, Thomas E Cox, et al.
Journal of the American Society of Nephrology : JASN|May 27, 2005
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndromeDavid Kavanagh, Elizabeth J Kemp, Elizabeth Mayland, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 29, 2011
Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bankHeather J Lambert, Aisling Stewart, Ambrose M Gullett, et al.
Blood|November 8, 2011
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndromeNigel J Francis, Bairbre McNicholas, Atif Awan, et al.
Molecular Immunology|June 29, 2007
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndromeDavid Kavanagh, Anna Richards, Marina Noris, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 10, 2010
Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulationChantal Loirat, Marie-Alice Macher, Monique Elmaleh-Berges, et al.
Journal of the American Society of Nephrology : JASN|February 23, 2013
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotypeElena Bresin, Erica Rurali, Jessica Caprioli, et al.
Plos Genetics|March 21, 2007
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndromePeter F Zipfel, Matthew Edey, Stefan Heinen, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 25, 2006
Complement factor H-associated atypical hemolytic uremic syndrome in monozygotic twins: concordant presentation, discordant response to treatmentJean-Claude Davin, Karolien H Olie, René Verlaak, et al.
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Immunobiology|June 9, 2016
Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndromePatrick J Gleeson, Valerie Wilson, Thomas E Cox, et al.
Journal of the American Society of Nephrology : JASN|May 27, 2005
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndromeDavid Kavanagh, Elizabeth J Kemp, Elizabeth Mayland, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 29, 2011
Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bankHeather J Lambert, Aisling Stewart, Ambrose M Gullett, et al.
Blood|November 8, 2011
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndromeNigel J Francis, Bairbre McNicholas, Atif Awan, et al.
Molecular Immunology|June 29, 2007
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndromeDavid Kavanagh, Anna Richards, Marina Noris, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 10, 2010
Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulationChantal Loirat, Marie-Alice Macher, Monique Elmaleh-Berges, et al.
Journal of the American Society of Nephrology : JASN|February 23, 2013
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotypeElena Bresin, Erica Rurali, Jessica Caprioli, et al.
Plos Genetics|March 21, 2007
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndromePeter F Zipfel, Matthew Edey, Stefan Heinen, et al.
Pageof 8