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Timothy H J Goodship

Showing results (51-60 of 78) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 23, 2013
Genotype/phenotype correlations in complement factor H deficiency arising from uniparental isodisomyValerie Wilson, Rebecca Darlay, William Wong, et al.
Journal of the American Society of Nephrology : JASN|December 5, 2009
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxHeather J Cordell, Rebecca Darlay, Pimphen Charoen, et al.
Blood Advances|January 4, 2018
Use of the complement inhibitor Coversin to treat HSCT-associated TMATimothy H J Goodship, Fernando Pinto, Wynn H Weston-Davies, et al.
Blood|October 29, 2009
Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndromeIain Moore, Lisa Strain, Isabel Pappworth, et al.
Journal of Medical Genetics|September 28, 2014
Factors determining penetrance in familial atypical haemolytic uraemic syndromeFrancis H Sansbury, Heather J Cordell, Coralie Bingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2003
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndromeAnna Richards, Elizabeth J Kemp, M Kathryn Liszewski, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 7, 2012
Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?David Kavanagh, Isabel Y Pappworth, Holly Anderson, et al.
Molecular Immunology|August 25, 2014
Autoantibodies to CD59, CD55, CD46 or CD35 are not associated with atypical haemolytic uraemic syndrome (aHUS)Rachael Watson, Emma Wearmouth, Amy-Claire McLoughlin, et al.
Kidney International|March 29, 2002
Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutationsCoralie Bingham, Sian Ellard, Trevor R P Cole, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 22, 2008
A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activityAnna M Blom, Frida Bergström, Matthew Edey, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 23, 2013
Genotype/phenotype correlations in complement factor H deficiency arising from uniparental isodisomyValerie Wilson, Rebecca Darlay, William Wong, et al.
Journal of the American Society of Nephrology : JASN|December 5, 2009
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxHeather J Cordell, Rebecca Darlay, Pimphen Charoen, et al.
Blood Advances|January 4, 2018
Use of the complement inhibitor Coversin to treat HSCT-associated TMATimothy H J Goodship, Fernando Pinto, Wynn H Weston-Davies, et al.
Blood|October 29, 2009
Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndromeIain Moore, Lisa Strain, Isabel Pappworth, et al.
Journal of Medical Genetics|September 28, 2014
Factors determining penetrance in familial atypical haemolytic uraemic syndromeFrancis H Sansbury, Heather J Cordell, Coralie Bingham, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2003
Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndromeAnna Richards, Elizabeth J Kemp, M Kathryn Liszewski, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 7, 2012
Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?David Kavanagh, Isabel Y Pappworth, Holly Anderson, et al.
Molecular Immunology|August 25, 2014
Autoantibodies to CD59, CD55, CD46 or CD35 are not associated with atypical haemolytic uraemic syndrome (aHUS)Rachael Watson, Emma Wearmouth, Amy-Claire McLoughlin, et al.
Kidney International|March 29, 2002
Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutationsCoralie Bingham, Sian Ellard, Trevor R P Cole, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 22, 2008
A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activityAnna M Blom, Frida Bergström, Matthew Edey, et al.
Pageof 8