ELENA
GOICOECHEA DE JORGE
Profesora contratada doctora
Hospital Universitario La Paz
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario La Paz (13)
2023
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Clinical Profiles and Patterns of Kidney Disease Progression in C3 Glomerulopathy
Kidney360, Vol. 4, Núm. 5, pp. 659-672
2022
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Development and validation of a nomogram to predict kidney survival at baseline in patients with C3 glomerulopathy
Clinical Kidney Journal, Vol. 15, Núm. 9, pp. 1737-1746
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Longitudinal change in proteinuria and kidney outcomes in C3 glomerulopathy
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, Vol. 37, Núm. 7, pp. 1270-1280
2021
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Validation of a Histologic Scoring Index for C3 Glomerulopathy
American Journal of Kidney Diseases, Vol. 77, Núm. 5, pp. 684-695.e1
2018
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Common and rare genetic variants of complement components in human disease
Molecular Immunology, Vol. 102, pp. 42-57
2017
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Elevated factor H–related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy
Kidney International, Vol. 92, Núm. 4, pp. 953-963
2008
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Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis
Molecular Immunology, Vol. 45, Núm. 10, pp. 2897-2904
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Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome
American Journal of Kidney Diseases, Vol. 52, Núm. 1, pp. 171-180
2007
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Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Núm. 1, pp. 240-245
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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 models
Human Mutation, Vol. 28, Núm. 3, pp. 222-234
2006
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Insights into hemolytic uremic syndrome: Segregation of three independent predisposition factors in a large, multiple affected pedigree
Molecular Immunology, Vol. 43, Núm. 11, pp. 1769-1775
2005
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Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32
Human Molecular Genetics, Vol. 14, Núm. 5, pp. 703-712
2004
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The human complement factor H: Functional roles, genetic variations and disease associations
Molecular Immunology, Vol. 41, Núm. 4, pp. 355-367