284 related articles for article (PubMed ID: 14978182)
1. Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.
Dragon-Durey MA; Frémeaux-Bacchi V; Loirat C; Blouin J; Niaudet P; Deschenes G; Coppo P; Herman Fridman W; Weiss L
J Am Soc Nephrol; 2004 Mar; 15(3):787-95. PubMed ID: 14978182
[TBL] [Abstract][Full Text] [Related]
2. Human complement factor H deficiency associated with hemolytic uremic syndrome.
Rougier N; Kazatchkine MD; Rougier JP; Fremeaux-Bacchi V; Blouin J; Deschenes G; Soto B; Baudouin V; Pautard B; Proesmans W; Weiss E; Weiss L
J Am Soc Nephrol; 1998 Dec; 9(12):2318-26. PubMed ID: 9848786
[TBL] [Abstract][Full Text] [Related]
3. Factor H and the pathogenesis of renal diseases.
Ault BH
Pediatr Nephrol; 2000 Sep; 14(10-11):1045-53. PubMed ID: 10975323
[TBL] [Abstract][Full Text] [Related]
4. An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations.
Saunders RE; Goodship TH; Zipfel PF; Perkins SJ
Hum Mutat; 2006 Jan; 27(1):21-30. PubMed ID: 16281287
[TBL] [Abstract][Full Text] [Related]
5. Hemolytic uremic syndrome due to homozygous factor H deficiency.
Sethi SK; Marie-Agnes DD; Thaker N; Hari P; Bagga A
Clin Exp Nephrol; 2009 Oct; 13(5):526-530. PubMed ID: 19568827
[TBL] [Abstract][Full Text] [Related]
6. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.
Servais A; Frémeaux-Bacchi V; Lequintrec M; Salomon R; Blouin J; Knebelmann B; Grünfeld JP; Lesavre P; Noël LH; Fakhouri F
J Med Genet; 2007 Mar; 44(3):193-9. PubMed ID: 17018561
[TBL] [Abstract][Full Text] [Related]
7. Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.
Vaziri-Sani F; Holmberg L; Sjöholm AG; Kristoffersson AC; Manea M; Frémeaux-Bacchi V; Fehrman-Ekholm I; Raafat R; Karpman D
Kidney Int; 2006 Mar; 69(6):981-8. PubMed ID: 16528247
[TBL] [Abstract][Full Text] [Related]
8. Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate.
Cho HY; Lee BS; Moon KC; Ha IS; Cheong HI; Choi Y
Pediatr Nephrol; 2007 Jun; 22(6):874-80. PubMed ID: 17295030
[TBL] [Abstract][Full Text] [Related]
9. Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome.
Abarrategui-Garrido C; Martínez-Barricarte R; López-Trascasa M; de Córdoba SR; Sánchez-Corral P
Blood; 2009 Nov; 114(19):4261-71. PubMed ID: 19745068
[TBL] [Abstract][Full Text] [Related]
10. Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case.
Gnappi E; Allinovi M; Vaglio A; Bresin E; Sorosina A; Pilato FP; Allegri L; Manenti L
Pediatr Nephrol; 2012 Oct; 27(10):1995-9. PubMed ID: 22669321
[TBL] [Abstract][Full Text] [Related]
11. Heterogeneous pattern of renal disease associated with homozygous factor H deficiency.
Servais A; Noël LH; Dragon-Durey MA; Gübler MC; Rémy P; Buob D; Cordonnier C; Makdassi R; Jaber W; Boulanger E; Lesavre P; Frémeaux-Bacchi V
Hum Pathol; 2011 Sep; 42(9):1305-11. PubMed ID: 21396679
[TBL] [Abstract][Full Text] [Related]
12. 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.
Saunders RE; Abarrategui-Garrido C; Frémeaux-Bacchi V; Goicoechea de Jorge E; Goodship TH; López Trascasa M; Noris M; Ponce Castro IM; Remuzzi G; Rodríguez de Córdoba S; Sánchez-Corral P; Skerka C; Zipfel PF; Perkins SJ
Hum Mutat; 2007 Mar; 28(3):222-34. PubMed ID: 17089378
[TBL] [Abstract][Full Text] [Related]
13. Complement factor H and hemolytic uremic syndrome.
Zipfel PF; Skerka C; Caprioli J; Manuelian T; Neumann HH; Noris M; Remuzzi G
Int Immunopharmacol; 2001 Mar; 1(3):461-8. PubMed ID: 11367530
[TBL] [Abstract][Full Text] [Related]
14. Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.
Pickering MC; Cook HT
Clin Exp Immunol; 2008 Feb; 151(2):210-30. PubMed ID: 18190458
[TBL] [Abstract][Full Text] [Related]
15. Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains.
Pickering MC; de Jorge EG; Martinez-Barricarte R; Recalde S; Garcia-Layana A; Rose KL; Moss J; Walport MJ; Cook HT; de Córdoba SR; Botto M
J Exp Med; 2007 Jun; 204(6):1249-56. PubMed ID: 17517971
[TBL] [Abstract][Full Text] [Related]
16. Atypical haemolytic uraemic syndrome and mutations in complement regulator genes.
Dragon-Durey MA; Frémeaux-Bacchi V
Springer Semin Immunopathol; 2005 Nov; 27(3):359-74. PubMed ID: 16189652
[TBL] [Abstract][Full Text] [Related]
17. Translational mini-review series on complement factor H: therapies of renal diseases associated with complement factor H abnormalities: atypical haemolytic uraemic syndrome and membranoproliferative glomerulonephritis.
Noris M; Remuzzi G
Clin Exp Immunol; 2008 Feb; 151(2):199-209. PubMed ID: 18070148
[TBL] [Abstract][Full Text] [Related]
18. Rare genetic variant in the CFB gene presenting as atypical hemolytic uremic syndrome and immune complex diffuse membranoproliferative glomerulonephritis, with crescents, successfully treated with eculizumab.
Alfakeeh K; Azar M; Alfadhel M; Abdullah AM; Aloudah N; Alsaad KO
Pediatr Nephrol; 2017 May; 32(5):885-891. PubMed ID: 28210841
[TBL] [Abstract][Full Text] [Related]
19. Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMD.
Goodship TH
Kidney Int; 2006 Jul; 70(1):12-3. PubMed ID: 16810287
[TBL] [Abstract][Full Text] [Related]
20. Genotype/phenotype correlations in complement factor H deficiency arising from uniparental isodisomy.
Wilson V; Darlay R; Wong W; Wood KM; McFarlane J; Schejbel L; Schmidt IM; Harris CL; Tellez J; Hunze EM; Marchbank K; Goodship JA; Goodship TH
Am J Kidney Dis; 2013 Nov; 62(5):978-83. PubMed ID: 23870792
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
