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T H J Goodship

Showing results (11-20 of 16) with videos related to

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Journal of Medical Genetics|March 24, 2005
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsV Fremeaux-Bacchi, E J Kemp, J A Goodship, et al.
Molecular Immunology|March 21, 2007
The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulationD Kavanagh, R Burgess, D Spitzer, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 3, 2009
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850TA M Waters, I Pappworth, K Marchbank, et al.
Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.
Journal of Thrombosis and Haemostasis : JTH|November 13, 2015
The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathiesE H Phillips, J P Westwood, V Brocklebank, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 17, 2012
Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantationJ H Brown, J Tellez, V Wilson, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Journal of Medical Genetics|March 24, 2005
The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsV Fremeaux-Bacchi, E J Kemp, J A Goodship, et al.
Molecular Immunology|March 21, 2007
The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulationD Kavanagh, R Burgess, D Spitzer, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 3, 2009
Successful renal transplantation in factor H autoantibody associated HUS with CFHR1 and 3 deficiency and CFH variant G2850TA M Waters, I Pappworth, K Marchbank, et al.
Molecular Immunology|March 23, 2010
Impact of compound heterozygous complement factor H mutations on development of atypical hemolytic uremic syndrome-A pedigree revisitedS A Johnson, J M Williams, S Hakobyan, et al.
Journal of Thrombosis and Haemostasis : JTH|November 13, 2015
The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathiesE H Phillips, J P Westwood, V Brocklebank, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 17, 2012
Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantationJ H Brown, J Tellez, V Wilson, et al.
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