-
1
-
-
0032974746
-
Factor H and disease: A complement regulator affects vital body functions
-
Zipfel PF, Hellwage J, Friese MA, Hegasy G, Jokiranta ST, Meri S. Factor H and disease: a complement regulator affects vital body functions. Mol Immunol 1999; 36: 241-248
-
(1999)
Mol. Immunol.
, vol.36
, pp. 241-248
-
-
Zipfel, P.F.1
Hellwage, J.2
Friese, M.A.3
Hegasy, G.4
Jokiranta, S.T.5
Meri, S.6
-
2
-
-
0033868902
-
Factor H and the pathogenesis of renal diseases
-
Ault BH. Factor H and the pathogenesis of renal diseases. Pediatr Nephrol 2000; 14: 1045-1053
-
(2000)
Pediatr. Nephrol.
, vol.14
, pp. 1045-1053
-
-
Ault, B.H.1
-
3
-
-
0032919054
-
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency
-
Warwicker P, Donne RL, Goodship JA et al. Familial relapsing haemolytic uraemic syndrome and complement factor H deficiency. Nephrol Dial Transplant 1999; 14: 1229-1233
-
(1999)
Nephrol. Dial. Transplant.
, vol.14
, pp. 1229-1233
-
-
Warwicker, P.1
Donne, R.L.2
Goodship, J.A.3
-
4
-
-
0031693194
-
Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H
-
Ohali M, Shalev H, Schlesinger M et al. Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H. Pediatr Nephrol 1998; 12: 619-624
-
(1998)
Pediatr. Nephrol.
, vol.12
, pp. 619-624
-
-
Ohali, M.1
Shalev, H.2
Schlesinger, M.3
-
5
-
-
0035143299
-
The molecular basis of familial hemolytic uremic syndrome: Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20
-
and the Italian Registry of Familial and Recurrent HUS/TTP
-
Caprioli J, Bettinaglio P, Zipfel PF et al. and the Italian Registry of Familial and Recurrent HUS/TTP. The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. J Am Soc Nephrol 2001; 12: 297-307
-
(2001)
J. Am. Soc. Nephrol.
, vol.12
, pp. 297-307
-
-
Caprioli, J.1
Bettinaglio, P.2
Zipfel, P.F.3
-
6
-
-
0022904646
-
Factor H deficiency in two brothers with atypical dense intramembranous deposit disease
-
Levy M, Halbwachs-Mecarelli L, Gubler MC et al. Factor H deficiency in two brothers with atypical dense intramembranous deposit disease. Kidney Int 1986; 30: 949-956
-
(1986)
Kidney Int.
, vol.30
, pp. 949-956
-
-
Levy, M.1
Halbwachs-Mecarelli, L.2
Gubler, M.C.3
-
7
-
-
0001727641
-
A familial deficiency of complement factor H
-
Lopez-Larrea C, Dieguez M, Enguix A, Dominguez O, Marin B, Gomez F. A familial deficiency of complement factor H. Biochem Soc Trans 1987; 15: 648-649
-
(1987)
Biochem. Soc. Trans.
, vol.15
, pp. 648-649
-
-
Lopez-Larrea, C.1
Dieguez, M.2
Enguix, A.3
Dominguez, O.4
Marin, B.5
Gomez, F.6
-
8
-
-
0028809266
-
Inherited factor H deficiency and collagen type III glomerulopathy
-
Vogt BA, Wyatt RJ, Burke BA, Simonton SC, Kashtan CE. Inherited factor H deficiency and collagen type III glomerulopathy. Pediatr Nephrol 1995; 9: 11-15
-
(1995)
Pediatr. Nephrol.
, vol.9
, pp. 11-15
-
-
Vogt, B.A.1
Wyatt, R.J.2
Burke, B.A.3
Simonton, S.C.4
Kashtan, C.E.5
-
9
-
-
0032986645
-
Long term effects of cyclosporine A in Alport's syndrome
-
Callis L, Vila A, Carrera M, Nieto J. Long term effects of cyclosporine A in Alport's syndrome. Kidney Int 1999; 55: 1051-1056
-
(1999)
Kidney Int.
, vol.55
, pp. 1051-1056
-
-
Callis, L.1
Vila, A.2
Carrera, M.3
Nieto, J.4
-
10
-
-
0347418134
-
Cyclosporine A slows the progressive renal disease of Alport Syndrome (X-Linked Hereditary Nephritis): Results of a canine model
-
Chen D, Jefferson B, Harvey SC et al. Cyclosporine A slows the progressive renal disease of Alport Syndrome (X-Linked Hereditary Nephritis): results of a canine model. J Am Soc Nephrol 2003; 14: 690-698
-
(2003)
J. Am. Soc. Nephrol.
, vol.14
, pp. 690-698
-
-
Chen, D.1
Jefferson, B.2
Harvey, S.C.3
-
11
-
-
0036699540
-
Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H
-
Pickering MC, Cook HT, Warren J et al. Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H. Nature Genet 2002; 31: 424-428
-
(2002)
Nature Genet.
, vol.31
, pp. 424-428
-
-
Pickering, M.C.1
Cook, H.T.2
Warren, J.3
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