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Timothy H J Goodship

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Kidney International|December 20, 2016
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceTimothy H J Goodship, H Terence Cook, Fadi Fakhouri, et al.
Human Mutation|February 14, 2006
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndromeStefan Heinen, Pilar Sanchez-Corral, Michael S Jackson, et al.
Plos Medicine|November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement geneJulian P Venables, Lisa Strain, Danny Routledge, et al.
Journal of the American Society of Nephrology : JASN|October 23, 2015
A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic SyndromeRachel C Challis, Geisilaine S R Araujo, Edwin K S Wong, et al.
Human Mutation|November 8, 2006
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural modelsRebecca E Saunders, Cynthia Abarrategui-Garrido, Véronique Frémeaux-Bacchi, et al.
Investigative Ophthalmology & Visual Science|July 2, 2010
Complement factor h autoantibodies and age-related macular degenerationBaljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Journal of the American Society of Nephrology : JASN|December 16, 2016
Thrombotic Microangiopathy in Inverted Formin 2<i>-</i>Mediated Renal DiseaseRachel C Challis, Troels Ring, Yaobo Xu, et al.
Molecular Immunology|June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritisTimothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Scientific Reports|January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Journal of the American Society of Nephrology : JASN|April 12, 2014
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GNEdwin K S Wong, Holly E Anderson, Andrew P Herbert, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Kidney International|December 20, 2016
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies ConferenceTimothy H J Goodship, H Terence Cook, Fadi Fakhouri, et al.
Human Mutation|February 14, 2006
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndromeStefan Heinen, Pilar Sanchez-Corral, Michael S Jackson, et al.
Plos Medicine|November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement geneJulian P Venables, Lisa Strain, Danny Routledge, et al.
Journal of the American Society of Nephrology : JASN|October 23, 2015
A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic SyndromeRachel C Challis, Geisilaine S R Araujo, Edwin K S Wong, et al.
Human Mutation|November 8, 2006
The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural modelsRebecca E Saunders, Cynthia Abarrategui-Garrido, Véronique Frémeaux-Bacchi, et al.
Investigative Ophthalmology & Visual Science|July 2, 2010
Complement factor h autoantibodies and age-related macular degenerationBaljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Journal of the American Society of Nephrology : JASN|December 16, 2016
Thrombotic Microangiopathy in Inverted Formin 2<i>-</i>Mediated Renal DiseaseRachel C Challis, Troels Ring, Yaobo Xu, et al.
Molecular Immunology|June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritisTimothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Scientific Reports|January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Journal of the American Society of Nephrology : JASN|April 12, 2014
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GNEdwin K S Wong, Holly E Anderson, Andrew P Herbert, et al.
Pageof 8