Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation

[1]  C. Sautès-Fridman,et al.  Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome. , 2010, Kidney international.

[2]  P. Barlow,et al.  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 syndrome. , 2010, Blood.

[3]  M. Mihatsch,et al.  C3 deposition glomerulopathy due to a functional factor H defect. , 2009, Kidney International.

[4]  V. D’Agati,et al.  Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients. , 2009, Clinical journal of the American Society of Nephrology : CJASN.

[5]  S. Rodríguez de Córdoba,et al.  Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis. , 2008, Molecular immunology.

[6]  B. Boudailliez,et al.  Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. , 2007, Journal of the American Society of Nephrology : JASN.

[7]  R. Salomon,et al.  A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation. , 2007, Molecular immunology.

[8]  R. Salomon,et al.  Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome , 2006, Journal of Medical Genetics.

[9]  P. Zipfel,et al.  Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II). , 2006, Kidney international.

[10]  A. Sjöholm,et al.  Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome. , 2006, Kidney international.

[11]  G. Deschênes,et al.  Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases. , 2004, Journal of the American Society of Nephrology : JASN.

[12]  C. West Idiopathic membranoproliferative glomerulonephritis in childhood , 2004, Pediatric Nephrology.

[13]  M. Walport,et al.  Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H , 2002, Nature Genetics.

[14]  N. Gretz,et al.  Complement analysis in children with idiopathic membranoproliferative glomerulonephritis: A long‐term follow‐up , 2001, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[15]  R. Portman,et al.  Changing patterns in the histopathology of idiopathic nephrotic syndrome in children. , 1999, Kidney international.

[16]  T. Srivastava,et al.  High incidence of focal segmental glomerulosclerosis in nephrotic syndrome of childhood , 1999, Pediatric Nephrology.

[17]  J. H. Jansen,et al.  Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency. , 1995, The Journal of clinical investigation.

[18]  T. Fujita,et al.  Significance of C3 nephritic factor (C3NeF) in non‐hypocomplementaemic serum with membranoproliferative glomerulonephritis (MPGN) , 1992, Clinical and experimental immunology.

[19]  C. López-Larrea,et al.  A familial deficiency of complement factor H , 1987 .

[20]  M. Gubler,et al.  H deficiency in two brothers with atypical dense intramembranous deposit disease. , 1986, Kidney international.

[21]  M. Gubler,et al.  Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (Type I MPGN) , 1978, Clinical immunology and immunopathology.

[22]  T. Cavallo,et al.  Membranoproliferative glomerulonephritis. Localization of early components of complement in glomerular deposits. , 1976, The American journal of pathology.

[23]  G. Schwartz,et al.  A simple estimate of glomerular filtration rate in children derived from body length and plasma creatinine , 1976, Pediatrics.

[24]  M. Gubler,et al.  Idiopathic membranoproliferative glomerulonephritis in children. Report of 105 cases. , 1973, Clinical Nephrology.

[25]  C. West,et al.  CHARACTERISTICS OF A NON-COMPLEMENT-DEPENDENT C3-REACTIVE COMPLEX FORMED FROM FACTORS IN NEPHRITIC AND NORMAL SERUM , 1970, The Journal of experimental medicine.