(Q33374215)

26 July 2017

Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate (English)

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atypical hemolytic uremic syndrome

26 July 2017

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Byong Sop Lee

2

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author name string

Hee Yeon Cho

1

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26 July 2017

Kyung Chul Moon

3

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26 July 2017

Il Soo Ha

4

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26 July 2017

Hae Il Cheong

5

1 reference

26 July 2017

Yong Choi

6

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26 July 2017

13 February 2007

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26 July 2017

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26 July 2017

22

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26 July 2017

6

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26 July 2017

874-880

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https://scigraph.springernature.com/pub.10.1007/s00467-007-0438-x

26 July 2017

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cites work

Inherited factor H deficiency and collagen type III glomerulopathy.

1 reference

12 December 2020

Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome

1 reference

12 December 2020

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

1 reference

12 December 2020

Hemolytic uremic syndrome: a fatal outcome after kidney and liver transplantation performed to correct factor h gene mutation

1 reference

12 December 2020

Atypical haemolytic uraemic syndrome

1 reference

12 December 2020

Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation

1 reference

12 December 2020

Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura

1 reference

12 December 2020

Collagen Type III Glomerulopathy: A New Idiopathic Glomerular Disease

1 reference

12 December 2020

Attempted treatment of factor H deficiency by liver transplantation

1 reference

12 December 2020

Genetic studies into inherited and sporadic hemolytic uremic syndrome

1 reference

12 December 2020

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

1 reference

12 December 2020

Complement factor H-associated atypical hemolytic uremic syndrome in monozygotic twins: concordant presentation, discordant response to treatment

1 reference

12 December 2020

Haemolytic uraemic syndrome following mumps, measles, and rubella vaccination

1 reference

12 December 2020

Renal transplantation in patients with hemolytic uremic syndrome: high rate of recurrence and increased incidence of acute rejections

1 reference

12 December 2020

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

1 reference

12 December 2020

MPGN II--genetically determined by defective complement regulation?

1 reference

12 December 2020

The role of defective complement control in hemolytic uremic syndrome

1 reference

12 December 2020

Factor H deficiency and fibrillary glomerulopathy

1 reference

12 December 2020

Familial haemolytic uraemic syndrome and an MCP mutation

1 reference

12 December 2020

Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

1 reference

12 December 2020

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

1 reference

12 December 2020

The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

1 reference

12 December 2020

Combined kidney and liver transplantation for familial haemolytic uraemic syndrome

1 reference

12 December 2020

Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15.

1 reference

12 December 2020

The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children

1 reference

12 December 2020

Renal transplantation in HUS patients with disorders of complement regulation

1 reference

12 December 2020

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

1 reference

12 December 2020

Membrane cofactor protein and factor I: mutations and transplantation

1 reference

12 December 2020

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

1 reference

12 December 2020

Recurrence of haemolytic-uraemic syndrome in renal transplants: a single-centre report

1 reference

12 December 2020

Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree

1 reference

12 December 2020

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

1 reference

12 December 2020

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

1 reference

12 December 2020

Complement dysfunction in hemolytic uremic syndrome

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12 December 2020

Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.

1 reference

12 December 2020

Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition

1 reference

12 December 2020

10.1007/S00467-007-0438-X

Identifiers

DOI

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Dimensions Publication ID

26 July 2017

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1 reference