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Complement factor H mutation associated with membranoproliferative glomerulonephritis with transformation to atypical haemolytic uraemic syndrome
Clinical Kidney Journal
◽
10.1093/ckj/sfs190
◽
2013
◽
Vol 6
(2)
◽
pp. 216-219
◽
Cited By ~ 11
Author(s):
K. Janssen van Doorn
◽
E. Dirinck
◽
G. A. Verpooten
◽
M. M. Couttenye
Keyword(s):
Membranoproliferative Glomerulonephritis
◽
Haemolytic Uraemic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
◽
Atypical Haemolytic Uraemic Syndrome
◽
Factor H Mutation
Download Full-text
Related Documents
Cited By
References
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
Clinical & Experimental Immunology
◽
10.1111/j.1365-2249.2007.03558.x
◽
2007
◽
Vol 151
(2)
◽
pp. 199-209
◽
Cited By ~ 22
Author(s):
M. Noris
◽
G. Remuzzi
Keyword(s):
Membranoproliferative Glomerulonephritis
◽
Haemolytic Uraemic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Renal Diseases
◽
Complement Factor
◽
Atypical Haemolytic Uraemic Syndrome
Download Full-text
Novel complement factor H gene mutation causing atypical haemolytic uraemic syndrome: early Eculizumab prevents acute dialysis
Clinical Kidney Journal
◽
10.1093/ckj/sfw132
◽
2017
◽
Vol 10
(2)
◽
pp. 263-265
Author(s):
James Collett
◽
Amali Mallawaarachchi
◽
Eddy Fischer
◽
Muralikrishna Gangadharan Komala
◽
Kamal Sud
◽
...
Keyword(s):
Gene Mutation
◽
Haemolytic Uraemic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
◽
Acute Dialysis
◽
Atypical Haemolytic Uraemic Syndrome
◽
H Gene
Download Full-text
Novel complement factor H mutation in SCR7 in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis type II
Molecular Immunology
◽
10.1016/j.molimm.2007.06.168
◽
2007
◽
Vol 44
(16)
◽
pp. 3973
Author(s):
Tamara Montes
◽
Rosa Ramos
◽
Rubén Martínez-Barricarte
◽
Sheila Pinto
◽
Monserrat Gomà
◽
...
Keyword(s):
Macular Degeneration
◽
Membranoproliferative Glomerulonephritis
◽
Factor H
◽
Age Related Macular Degeneration
◽
Complement Factor H
◽
Complement Factor
◽
Type Ii
◽
Age Related
◽
Factor H Mutation
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COMPLEMENT FACTOR H FUNCTIONAL ASSAY MAY HELP TO MONITOR ATYPICAL HAEMOLYTIC URAEMIC SYNDROME: A PILOT STUDY
Acta Clinica Belgica
◽
10.2143/acb.68.1.2062713
◽
2013
◽
Vol 68
(1)
◽
pp. 9-14
◽
Cited By ~ 1
Author(s):
A Massart
◽
S Golmarvi
◽
S Hachimi-Idrissi
◽
E Broeders
◽
Y Tournay
◽
...
Keyword(s):
Pilot Study
◽
Haemolytic Uraemic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Functional Assay
◽
Complement Factor
◽
Atypical Haemolytic Uraemic Syndrome
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Defects in complement Factor H-related proteins and susceptibility to atypical Haemolytic Uraemic Syndrome
Molecular Immunology
◽
10.1016/j.molimm.2013.05.119
◽
2013
◽
Vol 56
(3)
◽
pp. 281
Author(s):
M. Bernabéu-Herrero
◽
M. Jiménez-Alcázar
◽
S. Pinto
◽
M. López-Trascasa
◽
S. Rodríguez de Córdoba
◽
...
Keyword(s):
Haemolytic Uraemic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
◽
Atypical Haemolytic Uraemic Syndrome
◽
Related Proteins
Download Full-text
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
Journal of Medical Genetics
◽
10.1136/jmg.2008.064766
◽
2009
◽
Vol 46
(7)
◽
pp. 447-450
◽
Cited By ~ 108
Author(s):
M-A Dragon-Durey
◽
C Blanc
◽
F Marliot
◽
C Loirat
◽
J Blouin
◽
...
Keyword(s):
High Frequency
◽
Haemolytic Uraemic Syndrome
◽
Gene Deletion
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
◽
Atypical Haemolytic Uraemic Syndrome
Download Full-text
Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Mutation and IgA Nephropathy: A Case Report Successfully Treated with Eculizumab
Nephron
◽
10.1159/000485194
◽
2017
◽
Vol 138
(4)
◽
pp. 324-327
◽
Cited By ~ 6
Author(s):
Hironori Nakamura
◽
Mariko Anayama
◽
Mutsuki Makino
◽
Yasushi Makino
◽
Katsuhiko Tamura
◽
...
Keyword(s):
Case Report
◽
Hemolytic Uremic Syndrome
◽
Iga Nephropathy
◽
Atypical Hemolytic Uremic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
◽
Uremic Syndrome
◽
Factor H Mutation
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Glomerulonephritis associated with a novel factor H mutation and a large deletion in the complement factor H locus
Molecular Immunology
◽
10.1016/j.molimm.2009.05.197
◽
2009
◽
Vol 46
(14)
◽
pp. 2821-2822
Author(s):
L. Schejbel
◽
I.M. Schmidt
◽
H. Marquart
◽
P. Garred
Keyword(s):
Large Deletion
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
◽
Factor H Mutation
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Familial membranoproliferative glomerulonephritis type I associated with a functionally significant mutation in complement factor H
Immunobiology
◽
10.1016/j.imbio.2012.08.121
◽
2012
◽
Vol 217
(11)
◽
pp. 1171
Author(s):
Edwin Wong
◽
Holly Anderson
◽
Rachel Challis
◽
Andrew Herbert
◽
Paul Barlow
◽
...
Keyword(s):
Membranoproliferative Glomerulonephritis
◽
Factor H
◽
Complement Factor H
◽
Type I
◽
Complement Factor
◽
Membranoproliferative Glomerulonephritis Type I
Download Full-text
Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease
Human Molecular Genetics
◽
10.1093/hmg/ddg363
◽
2003
◽
Vol 12
(24)
◽
pp. 3385-3395
◽
Cited By ~ 228
Author(s):
Jessica Caprioli
◽
Federica Castelletti
◽
Sara Bucchioni
◽
Paola Bettinaglio
◽
Elena Bresin
◽
...
Keyword(s):
Gene Polymorphisms
◽
Haemolytic Uraemic Syndrome
◽
Factor H
◽
Complement Factor H
◽
Complement Factor
Download Full-text
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